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Graeme Bell

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Chemicals & Drugs

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Type 2 Diabetes Mellitus

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Amino Acid Sequence

Procedures

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Islets of Langerhans

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Co-Publications
Name
42
Cox, Nancy
26
Le Beau, Michelle
23
Xiang, Kun-san
22
Polonsky, Kenneth
21
Reisine, Terry
20
Iwasaki, Naoko
18
Steiner, Donald
17
Espinosa, Rafael
16
Horikawa, Yukio
13
Cockburn, Brian
13
Ogata, Makiko
12
Iwamoto, Yasuhiko
12
Philipson, Louis
12
Hattersley, Andrew
11
Hanis, Craig

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Publications

TOP 3
Kawai Toshihide; Ng Maggie C Y; Hayes M Geoffrey; Yoshiuchi Issei; Tsuchiya Takafumi; Robertson Heather; Cox Nancy J; Polonsky Kenneth S; Bell Graeme I; Ehrmann David A
Variation in the perilipin gene (PLIN) affects glucose and lipid metabolism in non-Hispanic white women with and without polycystic ovary syndrome.
Steiner D F; Park S-Y; Støy J; Philipson L H; Bell G I
A brief perspective on insulin production.
Park S-Y; Bell G I
Noninvasive monitoring of changes in pancreatic beta-cell mass by bioluminescent imaging in MIP-luc transgenic mice.

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All Publications

2009: Kawai Toshihide; Ng Maggie C Y; Hayes M Geoffrey; Yoshiuchi Issei; Tsuchiya Takafumi; Robertson Heather; Cox Nancy J; Polonsky Kenneth S; Bell Graeme I; Ehrmann David A
Variation in the perilipin gene (PLIN) affects glucose and lipid metabolism in non-Hispanic white women with and without polycystic ovary syndrome.
Diabetes research and clinical practice 2009;86(3):186-92.
2009: Steiner D F; Park S-Y; Støy J; Philipson L H; Bell G I
A brief perspective on insulin production.
Diabetes, obesity & metabolism 2009;11 Suppl 4():189-96.
2009: Park S-Y; Bell G I
Noninvasive monitoring of changes in pancreatic beta-cell mass by bioluminescent imaging in MIP-luc transgenic mice.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 2009;41(1):1-4.
2008: Støy Julie; Greeley Siri Atma W; Paz Veronica P; Ye Honggang; Pastore Ashley N; Skowron Kinga B; Lipton Rebecca B; Cogen Fran R; Bell Graeme I; Philipson Louis H;
Diagnosis and treatment of neonatal diabetes: a United States experience.
Pediatric diabetes 2008;9(5):450-9.
2008: Molven Anders; Ringdal Monika; Nordbø Anita M; Raeder Helge; Støy Julie; Lipkind Gregory M; Steiner Donald F; Philipson Louis H; Bergmann Ines; Aarskog Dagfinn; Undlien Dag E; Joner Geir; Søvik Oddmund; Bell Graeme I; Njølstad Pål R
Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes.
Diabetes 2008;57(4):1131-5.
2008: Edghill Emma L; Flanagan Sarah E; Patch Ann-Marie; Boustred Chris; Parrish Andrew; Shields Beverley; Shepherd Maggie H; Hussain Khalid; Kapoor Ritika R; Malecki Maciej; MacDonald Michael J; Støy Julie; Steiner Donald F; Philipson Louis H; Bell Graeme I; Hattersley Andrew T; Ellard Sian
Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.
Diabetes 2008;57(4):1034-42.
2007: Hayes M Geoffrey; Pluzhnikov Anna; Miyake Kazuaki; Sun Ying; Ng Maggie C Y; Roe Cheryl A; Below Jennifer E; Nicolae Raluca I; Konkashbaev Anuar; Bell Graeme I; Cox Nancy J; Hanis Craig L
Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies.
Diabetes 2007;56(12):3033-44.
2007: Hara M; Shen J; Pugh W; Polonsky K S; Le Beau M M; Bell G I
Sustained expression of hepatocyte nuclear factor-6 leads to loss of pancreatic beta-cells by apoptosis.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2007;115(10):654-61.
2007: Støy Julie; Edghill Emma L; Flanagan Sarah E; Ye Honggang; Paz Veronica P; Pluzhnikov Anna; Below Jennifer E; Hayes M Geoffrey; Cox Nancy J; Lipkind Gregory M; Lipton Rebecca B; Greeley Siri Atma W; Patch Ann-Marie; Ellard Sian; Steiner Donald F; Hattersley Andrew T; Philipson Louis H; Bell Graeme I;
Insulin gene mutations as a cause of permanent neonatal diabetes.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(38):15040-4.
2006: Hathout Eba; Mace John; Bell Graeme I; Njølstad Pål R
Treatment of hyperglycemia in a 7-year-old child diagnosed with neonatal diabetes.
Diabetes care 2006;29(6):1458.
2006: Sagen Jørn V; Odili Stella; Bjørkhaug Lise; Zelent Dorothy; Buettger Carol; Kwagh Jae; Stanley Charles; Dahl-Jørgensen Knut; de Beaufort Carine; Bell Graeme I; Han Yi; Grimsby Joseph; Taub Rebecca; Molven Anders; Søvik Oddmund; Njølstad Pål R; Matschinsky Franz M
From clinicogenetic studies of maturity-onset diabetes of the young to unraveling complex mechanisms of glucokinase regulation.
Diabetes 2006;55(6):1713-22.
2005: Hayes M Geoffrey; del Bosque-Plata Laura; Tsuchiya Takafumi; Hanis Craig L; Bell Graeme I; Cox Nancy J
Patterns of linkage disequilibrium in the type 2 diabetes gene calpain-10.
Diabetes 2005;54(12):3573-6.
2005: Ng M C Y; Miyake K; So W Y; Poon E W M; Lam V K L; Li J K Y; Cox N J; Bell G I; Chan J C N
The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population.
Diabetologia 2005;48(10):2018-24.
2005: Park Soo-Young; Wang Xiaoyu; Chen Zhongyi; Powers Alvin C; Magnuson Mark A; Head W Steven; Piston David W; Bell Graeme I
Optical imaging of pancreatic beta cells in living mice expressing a mouse insulin I promoter-firefly luciferase transgene.
Genesis (New York, N.Y. : 2000) 2005;43(2):80-6.
2005: Grasberger Helmut; Bell Graeme I
Subcellular recruitment by TSG118 and TSPYL implicates a role for zinc finger protein 106 in a novel developmental pathway.
The international journal of biochemistry & cell biology 2005;37(7):1421-37.
2005: Xie Jing-Tian; Mehendale Sangeeta R; Li Xinmin; Quigg Richard; Wang Xiaoyu; Wang Chong-Zhi; Wu Ji An; Aung Han H; A Rue Paul; Bell Graeme I; Yuan Chun-Su
Anti-diabetic effect of ginsenoside Re in ob/ob mice.
Biochimica et biophysica acta 2005;1740(3):319-25.
2005: Cockburn B N; Bermano G; Boodram L L; Teelucksingh S; Tsuchiya T; Mahabir D; Allan A B; Stein R; Docherty K; Bell G I
Gene symbol: IPF1. Disease: MODY 4.
Human genetics 2005;116(6):538.
2005: Wang Chang-Zheng; Wang Yong; Di Anke; Magnuson Mark A; Ye Honggang; Roe Michael W; Nelson Deborah J; Bell Graeme I; Philipson Louis H
5-amino-imidazole carboxamide riboside acutely potentiates glucose-stimulated insulin secretion from mouse pancreatic islets by KATP channel-dependent and -independent pathways.
Biochemical and biophysical research communications 2005;330(4):1073-9.
2005: Gunawardana Subhadra C; Hara Manami; Bell Graeme I; Head W Steven; Magnuson Mark A; Piston David W
Imaging Beta cell development in real-time using pancreatic explants from mice with green fluorescent protein-labeled pancreatic Beta cells.
In vitro cellular & developmental biology. Animal 2005;41(1-2):7-11.
2005: Grasberger Helmut; Ye Honggang; Mashima Hirosato; Bell Graeme I
Dual promoter structure of ZFP106: regulation by myogenin and nuclear respiratory factor-1.
Gene 2005;344():143-59.
2005: Iwasaki Naoko; Horikawa Yukio; Tsuchiya Takafumi; Kitamura Yutaka; Nakamura Takahiro; Tanizawa Yukio; Oka Yoshitomo; Hara Kazuo; Kadowaki Takashi; Awata Takuya; Honda Masashi; Yamashita Katsuko; Oda Naohisa; Yu Li; Yamada Norihiro; Ogata Makiko; Kamatani Naoyuki; Iwamoto Yasuhiko; Del Bosque-Plata Laura; Hayes M Geoffrey; Cox Nancy J; Bell Graeme I
Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population.
Journal of human genetics 2005;50(2):92-8.
2004: Sagen Jørn V; Raeder Helge; Hathout Eba; Shehadeh Naim; Gudmundsson Kolbeinn; Baevre Halvor; Abuelo Dianne; Phornphutkul Chanika; Molnes Janne; Bell Graeme I; Gloyn Anna L; Hattersley Andrew T; Molven Anders; Søvik Oddmund; Njølstad Pål R
Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy.
Diabetes 2004;53(10):2713-8.
2004: Ng Maggie C Y; So Wing-Yee; Lam Vincent K L; Cockram Clive S; Bell Graeme I; Cox Nancy J; Chan Juliana C N
Genome-wide scan for metabolic syndrome and related quantitative traits in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25.
Diabetes 2004;53(10):2676-83.
2004: Alcoser Sergio Y; Hara Manami; Bell Graeme I; Ehrmann David A
Association of the (AU)AT-rich element polymorphism in PPP1R3 with hormonal and metabolic features of polycystic ovary syndrome.
The Journal of clinical endocrinology and metabolism 2004;89(6):2973-6.
2004: Ng Maggie C Y; So Wing-Yee; Cox Nancy J; Lam Vincent K L; Cockram Clive S; Critchley Julian A J H; Bell Graeme I; Chan Juliana C N
Genome-wide scan for type 2 diabetes loci in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25.
Diabetes 2004;53(6):1609-13.
2004: Cockburn Brian N; Bermano Giovanna; Boodram Laura-Lee G; Teelucksingh Surujpal; Tsuchiya Takafumi; Mahabir Deepak; Allan Andrew B; Stein Roland; Docherty Kevin; Bell Graeme I
Insulin promoter factor-1 mutations and diabetes in Trinidad: identification of a novel diabetes-associated mutation (E224K) in an Indo-Trinidadian family.
The Journal of clinical endocrinology and metabolism 2004;89(2):971-8.
2004: Cox Nancy J; Hayes M Geoffrey; Roe Cheryl A; Tsuchiya Takafumi; Bell Graeme I
Linkage of calpain 10 to type 2 diabetes: the biological rationale.
Diabetes 2004;53 Suppl 1():S19-25.
2004: del Bosque-Plata Laura; Aguilar-Salinas Carlos A; Tusié-Luna María Teresa; Ramírez-Jiménez Salvador; Rodríguez-Torres Maribel; Aurón-Gómez Moisés; Ramírez Erika; Velasco-Pérez María Luisa; Ramírez-Silva Alfredo; Gómez-Pérez Francisco; Hanis Craig L; Tsuchiya Takafumi; Yoshiuchi Issei; Cox Nancy J; Bell Graeme I
Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population.
Molecular genetics and metabolism 2004;81(2):122-6.
2003: So W Y; Ng Maggie C Y; Horikawa Yukio; Njølstad Pal R; Li June K Y; Ma Ronald C W; Bell Graeme I; Chan Juliana C N
Genetic variants of hepatocyte nuclear factor-1beta in Chinese young-onset diabetic patients with nephropathy.
Journal of diabetes and its complications 2003;17(6):369-73.
2003: Weedon Michael N; Schwarz Peter E H; Horikawa Yukio; Iwasaki Naoko; Illig Thomas; Holle Rolf; Rathmann Wolfgang; Selisko Thomas; Schulze Jan; Owen Katherine R; Evans Julie; Del Bosque-Plata Laura; Hitman Graham; Walker Mark; Levy Jonathan C; Sampson Mike; Bell Graeme I; McCarthy Mark I; Hattersley Andrew T; Frayling Timothy M
Meta-analysis and a large association study confirm a role for calpain-10 variation in type 2 diabetes susceptibility.
American journal of human genetics 2003;73(5):1208-12.
2003: Naoumova Rossitza P; Bonney Stephanie A; Eichenbaum-Voline Sophie; Patel Hetal N; Jones Bethan; Jones Emma L; Amey Joanna; Colilla Susan; Neuwirth Clare K Y; Allotey Rebecca; Seed Mary; Betteridge D John; Galton David J; Cox Nancy J; Bell Graeme I; Scott James; Shoulders Carol C
Confirmed locus on chromosome 11p and candidate loci on 6q and 8p for the triglyceride and cholesterol traits of combined hyperlipidemia.
Arteriosclerosis, thrombosis, and vascular biology 2003;23(11):2070-7.
2003: Zhou Yun-Ping; Sreenan Seamus; Pan Chien-Yuan; Currie Kevin P M; Bindokas Vytautas P; Horikawa Yukio; Lee Jean-Pyo; Ostrega Diane; Ahmed Noreen; Baldwin Aaron C; Cox Nancy J; Fox Aaron P; Miller Richard J; Bell Graeme I; Polonsky Kenneth S
A 48-hour exposure of pancreatic islets to calpain inhibitors impairs mitochondrial fuel metabolism and the exocytosis of insulin.
Metabolism: clinical and experimental 2003;52(5):528-34.
2003: Canizales-Quinteros Samuel; Aguilar-Salinas Carlos A; Reyes-Rodríguez Eduardo; Riba Laura; Rodríguez-Torres Maribel; Ramírez-Jiménez Salvador; Huertas-Vázquez Adriana; Fragoso-Ontiveros Verónica; Zentella-Dehesa Alejandro; Ventura-Gallegos José L; Vega-Hernández Gerardo; López-Estrada Angelina; Aurón-Gómez Moisés; Gómez-Pérez Francisco; Rull Juan; Cox Nancy J; Bell Graeme I; Tusié-Luna Maria Teresa
Locus on chromosome 6p linked to elevated HDL cholesterol serum levels and to protection against premature atherosclerosis in a kindred with familial hypercholesterolemia.
Circulation research 2003;92(5):569-76.
2003: Iwasaki Naoko; Cox Nancy J; Wang Yan-Qing; Schwarz Peter E H; Bell Graeme I; Honda Masashi; Imura Mitsuo; Ogata Makiko; Saito Masayuki; Kamatani Naoyuki; Iwamoto Yasuhiko
Mapping genes influencing type 2 diabetes risk and BMI in Japanese subjects.
Diabetes 2003;52(1):209-13.
2003: Hara Manami; Wang Xiaoyu; Kawamura Toshihiko; Bindokas Vytas P; Dizon Restituto F; Alcoser Sergio Y; Magnuson Mark A; Bell Graeme I
Transgenic mice with green fluorescent protein-labeled pancreatic beta -cells.
American journal of physiology. Endocrinology and metabolism 2003;284(1):E177-83.
2002: Rasmussen Søren K; Urhammer Søren A; Berglund Lars; Jensen Jan N; Hansen Lars; Echwald Søren M; Borch-Johnsen Knut; Horikawa Yukio; Mashima Hirosato; Lithell Hans; Cox Nancy J; Hansen Torben; Bell Graeme I; Pedersen Oluf
Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians.
Diabetes 2002;51(12):3561-7.
2002: Ehrmann David A; Tang Xu; Yoshiuchi Issei; Cox Nancy J; Bell Graeme I
Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome.
The Journal of clinical endocrinology and metabolism 2002;87(9):4297-300.
2002: Haddad Lema; Evans Julie C; Gharani Neda; Robertson Carole; Rush Karen; Wiltshire Steven; Frayling Timothy M; Wilkin Terence J; Demaine Andrew; Millward Ann; Hattersley Andrew T; Conway Gerry; Cox Nancy J; Bell Graeme I; Franks Steve; McCarthy Mark I
Variation within the type 2 diabetes susceptibility gene calpain-10 and polycystic ovary syndrome.
The Journal of clinical endocrinology and metabolism 2002;87(6):2606-10.
2002: Fullerton Stephanie M; Bartoszewicz Angelika; Ybazeta Gustavo; Horikawa Yukio; Bell Graeme I; Kidd Kenneth K; Cox Nancy J; Hudson Richard R; Di Rienzo Anna
Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus.
American journal of human genetics 2002;70(5):1096-106.
2002: Ehrmann David A; Schwarz Peter E H; Hara Manami; Tang Xu; Horikawa Yukio; Imperial Jacqueline; Bell Graeme I; Cox Nancy J
Relationship of calpain-10 genotype to phenotypic features of polycystic ovary syndrome.
The Journal of clinical endocrinology and metabolism 2002;87(4):1669-73.
2002: Ogata Makiko; Awaji Takeo; Iwasaki Naoko; Miyazaki Shunichi; Bell Graeme I; Iwamoto Yasuhiko
Nuclear translocation of SHP and visualization of interaction with HNF-4alpha in living cells.
Biochemical and biophysical research communications 2002;292(1):8-12.
2002: Forsythe Sean M; Kogut Paul C; McConville John F; Fu Yiping; McCauley Joel A; Halayko Andrew J; Liu Hong Wei; Kao Allen; Fernandes Darren J; Bellam Shashi; Fuchs Elaine; Sinha Satrajit; Bell Graeme I; Camoretti-Mercado Blanca; Solway Julian
Structure and transcription of the human m3 muscarinic receptor gene.
American journal of respiratory cell and molecular biology 2002;26(3):298-305.
2001: Sreenan S K; Zhou Y P; Otani K; Hansen P A; Currie K P; Pan C Y; Lee J P; Ostrega D M; Pugh W; Horikawa Y; Cox N J; Hanis C L; Burant C F; Fox A P; Bell G I; Polonsky K S
Calpains play a role in insulin secretion and action.
Diabetes 2001;50(9):2013-20.
2001: Evans J C; Frayling T M; Cassell P G; Saker P J; Hitman G A; Walker M; Levy J C; O'Rahilly S; Rao P V; Bennett A J; Jones E C; Menzel S; Prestwich P; Simecek N; Wishart M; Dhillon R; Fletcher C; Millward A; Demaine A; Wilkin T; Horikawa Y; Cox N J; Bell G I; Ellard S; McCarthy M I; Hattersley A T
Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom.
American journal of human genetics 2001;69(3):544-52.
2001: Njølstad P R; Søvik O; Cuesta-Muñoz A; Bjørkhaug L; Massa O; Barbetti F; Undlien D E; Shiota C; Magnuson M A; Molven A; Matschinsky F M; Bell G I
Neonatal diabetes mellitus due to complete glucokinase deficiency.
The New England journal of medicine 2001;344(21):1588-92.
2001: del Bosque-Plata L; Lin J; Horikawa Y; Schwarz P E; Cox N J; Iwasaki N; Ogata M; Iwamoto Y; German M S; Bell G I
Mutations in the coding region of the neurogenin 3 gene (NEUROG3) are not a common cause of maturity-onset diabetes of the young in Japanese subjects.
Diabetes 2001;50(3):694-6.
2001: Hara M; Wang X; Paz V P; Iwasaki N; Honda M; Iwamoto Y; Bell G I
Identification of three missense mutations in the peroxisome proliferator-activated receptor alpha gene in Japanese subjects with maturity-onset diabetes of the young.
Journal of human genetics 2001;46(5):285-8.
2000: Horikawa Y; Horikawa Y; Cox N J; Iwasaki N; Ogata M; Iwamoto Y; Schwitzgebel V; German M S; Bell G I
beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4 (NEUROD4) in Japanese patients with MODY.
Diabetes 2000;49(11):1955-7.
2000: Horikawa Y; Oda N; Cox N J; Li X; Orho-Melander M; Hara M; Hinokio Y; Lindner T H; Mashima H; Schwarz P E; del Bosque-Plata L; Horikawa Y; Oda Y; Yoshiuchi I; Colilla S; Polonsky K S; Wei S; Concannon P; Iwasaki N; Schulze J; Baier L J; Bogardus C; Groop L; Boerwinkle E; Hanis C L; Bell G I
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.
Nature genetics 2000;26(2):163-75.
2000: Hara M; Wang X; Paz V P; Cox N J; Iwasaki N; Ogata M; Iwamoto Y; Bell G I
No diabetes-associated mutations in the coding region of the hepatocyte nuclear factor-4gamma gene (HNF4G) in Japanese patients with MODY.
Diabetologia 2000;43(8):1064-9.
2000: Bjørkhaug L; Søvik O; Bell G I; Njølstad P R; Molven A
A simple test for the high-frequency P291fsinsC mutation in the HNF1 alpha/MODY3 gene.
Diabetologia 2000;43(6):818-9.
2000: Bingham C; Ellard S; Allen L; Bulman M; Shepherd M; Frayling T; Berry P J; Clark P M; Lindner T; Bell G I; Ryffel G U; Nicholls A J; Hattersley A T
Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta.
Kidney international 2000;57(3):898-907.
2000: Hinokio Y; Horikawa Y; Furuta H; Cox N J; Iwasaki N; Honda M; Ogata M; Iwamoto Y; Bell G I
Beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3beta gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young.
Diabetes 2000;49(2):302-5.
1999: Ng M C; Cockburn B N; Lindner T H; Yeung V T; Chow C C; So W Y; Li J K; Lo Y M; Lee Z S; Cockram C S; Critchley J A; Bell G I; Chan J C
Molecular genetics of diabetes mellitus in Chinese subjects: identification of mutations in glucokinase and hepatocyte nuclear factor-1alpha genes in patients with early-onset type 2 diabetes mellitus/MODY.
Diabetic medicine : a journal of the British Diabetic Association 1999;16(11):956-63.
1999: Lindner T H; Njolstad P R; Horikawa Y; Bostad L; Bell G I; Sovik O
A novel syndrome of diabetes mellitus, renal dysfunction and genital malformation associated with a partial deletion of the pseudo-POU domain of hepatocyte nuclear factor-1beta.
Human molecular genetics 1999;8(11):2001-8.
1999: Rouard M; Bass J; Grigorescu F; Garrett T P; Ward C W; Lipkind G; Jaffiole C; Steiner D F; Bell G I
Congenital insulin resistance associated with a conformational alteration in a conserved beta-sheet in the insulin receptor L1 domain.
The Journal of biological chemistry 1999;274(26):18487-91.
1999: Hathout E H; Cockburn B N; Mace J W; Sharkey J; Chen-Daniel J; Bell G I
A case of hepatocyte nuclear factor-1 alpha diabetes/MODY3 masquerading as type 1 diabetes in a Mexican-American adolescent and responsive to a low dose of sulfonylurea.
Diabetes care 1999;22(5):867-8.
1999: Cox N J; Frigge M; Nicolae D L; Concannon P; Hanis C L; Bell G I; Kong A
Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans.
Nature genetics 1999;21(2):213-5.
1999: Lindner T H; Cockburn B N; Bell G I
Molecular genetics of MODY in Germany.
Diabetologia 1999;42(1):121-3.
1998: Sreenan S K; Cockburn B N; Baldwin A C; Ostrega D M; Levisetti M; Grupe A; Bell G I; Stewart T A; Roe M W; Polonsky K S
Adaptation to hyperglycemia enhances insulin secretion in glucokinase mutant mice.
Diabetes 1998;47(12):1881-8.
1998: Dukes I D; Sreenan S; Roe M W; Levisetti M; Zhou Y P; Ostrega D; Bell G I; Pontoglio M; Yaniv M; Philipson L; Polonsky K S
Defective pancreatic beta-cell glycolytic signaling in hepatocyte nuclear factor-1alpha-deficient mice.
The Journal of biological chemistry 1998;273(38):24457-64.
1998: Njølstad P R; Cockburn B N; Bell G I; Søvik O
A missense mutation, Val62Ala, in the glucokinase gene in a Norwegian family with maturity-onset diabetes of the young.
Acta paediatrica (Oslo, Norway : 1992) 1998;87(8):853-6.
1998: Furuta H; Horikawa Y; Iwasaki N; Hara M; Sussel L; Le Beau M M; Davis E M; Ogata M; Iwamoto Y; German M S; Bell G I
Beta-cell transcription factors and diabetes: mutations in the coding region of the BETA2/NeuroD1 (NEUROD1) and Nkx2.2 (NKX2B) genes are not associated with maturity-onset diabetes of the young in Japanese.
Diabetes 1998;47(8):1356-8.
1998: Beards F; Frayling T; Bulman M; Horikawa Y; Allen L; Appleton M; Bell G I; Ellard S; Hattersley A T
Mutations in hepatocyte nuclear factor 1beta are not a common cause of maturity-onset diabetes of the young in the U.K.
Diabetes 1998;47(7):1152-4.
1998: Søvik O; Njølstad P; Følling I; Sagen J; Cockburn B N; Bell G I
Hyperexcitability to sulphonylurea in MODY3.
Diabetologia 1998;41(5):607-8.
1998: Pontoglio M; Sreenan S; Roe M; Pugh W; Ostrega D; Doyen A; Pick A J; Baldwin A; Velho G; Froguel P; Levisetti M; Bonner-Weir S; Bell G I; Yaniv M; Polonsky K S
Defective insulin secretion in hepatocyte nuclear factor 1alpha-deficient mice.
The Journal of clinical investigation 1998;101(10):2215-22.
1998: Hara M; Lindner T H; Paz V P; Wang X; Iwasaki N; Ogata M; Iwamoto Y; Bell G I
Mutations in the coding region of the insulin promoter factor 1 gene are not a common cause of maturity-onset diabetes of the young in Japanese subjects.
Diabetes 1998;47(5):845-6.
1998: Njølstad P R; Søvik O; Bell G I; Cockburn B N; Følling I; Sagen J
[Non-insulin dependent diabetes in children and adolescents]
Tidsskrift for den Norske lægeforening : tidsskrift for praktisk medicin, ny række 1998;118(7):1054-7.
1997: Horikawa Y; Iwasaki N; Hara M; Furuta H; Hinokio Y; Cockburn B N; Lindner T; Yamagata K; Ogata M; Tomonaga O; Kuroki H; Kasahara T; Iwamoto Y; Bell G I
Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.
Nature genetics 1997;17(4):384-5.
1997: Furuta H; Iwasaki N; Oda N; Hinokio Y; Horikawa Y; Yamagata K; Yano N; Sugahiro J; Ogata M; Ohgawara H; Omori Y; Iwamoto Y; Bell G I
Organization and partial sequence of the hepatocyte nuclear factor-4 alpha/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY.
Diabetes 1997;46(10):1652-7.
1997: Gragnoli C; Lindner T; Cockburn B N; Kaisaki P J; Gragnoli F; Marozzi G; Bell G I
Maturity-onset diabetes of the young due to a mutation in the hepatocyte nuclear factor-4 alpha binding site in the promoter of the hepatocyte nuclear factor-1 alpha gene.
Diabetes 1997;46(10):1648-51.
1997: Chien E K; Tokuyama Y; Rouard M; Phillippe M; Bell G I
Identification of gestationally regulated genes in rat myometrium by use of messenger ribonucleic acid differential display.
American journal of obstetrics and gynecology 1997;177(3):645-52.
1997: Lindner T; Gragnoli C; Furuta H; Cockburn B N; Petzold C; Rietzsch H; Weiss U; Schulze J; Bell G I
Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4alpha/MODY1 gene.
The Journal of clinical investigation 1997;100(6):1400-5.
1997: Iwasaki N; Oda N; Ogata M; Hara M; Hinokio Y; Oda Y; Yamagata K; Kanematsu S; Ohgawara H; Omori Y; Bell G I
Mutations in the hepatocyte nuclear factor-1alpha/MODY3 gene in Japanese subjects with early- and late-onset NIDDM.
Diabetes 1997;46(9):1504-8.
1997: Cockburn B N; Ostrega D M; Sturis J; Kubstrup C; Polonsky K S; Bell G I
Changes in pancreatic islet glucokinase and hexokinase activities with increasing age, obesity, and the onset of diabetes.
Diabetes 1997;46(9):1434-9.
1997: Chien E K; Hara M; Rouard M; Yano H; Phillippe M; Polonsky K S; Bell G I
Increase in serum leptin and uterine leptin receptor messenger RNA levels during pregnancy in rats.
Biochemical and biophysical research communications 1997;237(2):476-80.
1997: Lindner T; Gragnoli C; Schulze J; Rietzsch H; Petzold C; Schröder H E; Cox N J; Bell G I
The 31-cM region of chromosome 11 including the obesity gene tubby and ATP-sensitive potassium channel genes, SUR1 and Kir6.2, does not contain a major susceptibility locus for NIDDM in 127 non-Hispanic white affected sibships.
Diabetes 1997;46(7):1227-9.
1997: Urhammer S A; Rasmussen S K; Kaisaki P J; Oda N; Yamagata K; Møller A M; Fridberg M; Hansen L; Hansen T; Bell G I; Pedersen O
Genetic variation in the hepatocyte nuclear factor-1 alpha gene in Danish Caucasians with late-onset NIDDM.
Diabetologia 1997;40(4):473-5.
1997: Vaxillaire M; Rouard M; Yamagata K; Oda N; Kaisaki P J; Boriraj V V; Chevre J C; Boccio V; Cox R D; Lathrop G M; Dussoix P; Philippe J; Timsit J; Charpentier G; Velho G; Bell G I; Froguel P
Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3).
Human molecular genetics 1997;6(4):583-6.
1997: Hansen T; Eiberg H; Rouard M; Vaxillaire M; Møller A M; Rasmussen S K; Fridberg M; Urhammer S A; Holst J J; Almind K; Echwald S M; Hansen L; Bell G I; Pedersen O
Novel MODY3 mutations in the hepatocyte nuclear factor-1alpha gene: evidence for a hyperexcitability of pancreatic beta-cells to intravenous secretagogues in a glucose-tolerant carrier of a P447L mutation.
Diabetes 1997;46(4):726-30.
1997: Frayling T M; Bulamn M P; Ellard S; Appleton M; Dronsfield M J; Mackie A D; Baird J D; Kaisaki P J; Yamagata K; Bell G I; Bain S C; Hattersley A T
Mutations in the hepatocyte nuclear factor-1alpha gene are a common cause of maturity-onset diabetes of the young in the U.K.
Diabetes 1997;46(4):720-5.
1997: Kaisaki P J; Menzel S; Lindner T; Oda N; Rjasanowski I; Sahm J; Meincke G; Schulze J; Schmechel H; Petzold C; Ledermann H M; Sachse G; Boriraj V V; Menzel R; Kerner W; Turner R C; Yamagata K; Bell G I
Mutations in the hepatocyte nuclear factor-1alpha gene in MODY and early-onset NIDDM: evidence for a mutational hotspot in exon 4.
Diabetes 1997;46(3):528-35.
1996: Yamagata K; Furuta H; Oda N; Kaisaki P J; Menzel S; Cox N J; Fajans S S; Signorini S; Stoffel M; Bell G I
Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1)
Nature 1996;384(6608):458-60.
1996: Yamagata K; Oda N; Kaisaki P J; Menzel S; Furuta H; Vaxillaire M; Southam L; Cox R D; Lathrop G M; Boriraj V V; Chen X; Cox N J; Oda Y; Yano H; Le Beau M M; Yamada S; Nishigori H; Takeda J; Fajans S S; Hattersley A T; Iwasaki N; Hansen T; Pedersen O; Polonsky K S; Bell G I
Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)
Nature 1996;384(6608):455-8.
1996: Semina E V; Datson N A; Leysens N J; Zabel B U; Carey J C; Bell G I; Bitoun P; Lindgren C; Stevenson T; Frants R R; van Ommen G; Murray J C
Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus.
American journal of human genetics 1996;59(6):1288-96.
1996: Byrne M M; Sturis J; Menzel S; Yamagata K; Fajans S S; Dronsfield M J; Bain S C; Hattersley A T; Velho G; Froguel P; Bell G I; Polonsky K S
Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12.
Diabetes 1996;45(11):1503-10.
1996: Hino A; Tokuyama Y; Weir B; Takeda J; Yano H; Bell G I; Macdonald R L
Changes in endothelial nitric oxide synthase mRNA during vasospasm after subarachnoid hemorrhage in monkeys.
Neurosurgery 1996;39(3):562-7; discussion 567-8.
1996: Furuta H; Nishi S; Le Beau M M; Fernald A A; Yano H; Bell G I
Sequence of human hexokinase III cDNA and assignment of the human hexokinase III gene (HK3) to chromosome band 5q35.2 by fluorescence in situ hybridization.
Genomics 1996;36(1):206-9.
1996: Glaum S R; Hara M; Bindokas V P; Lee C C; Polonsky K S; Bell G I; Miller R J
Leptin, the obese gene product, rapidly modulates synaptic transmission in the hypothalamus.
Molecular pharmacology 1996;50(2):230-5.
1996: Hino A; Tokuyama Y; Kobayashi M; Yano M; Weir B; Takeda J; Wang X; Bell G I; Macdonald R L
Increased expression of endothelin B receptor mRNA following subarachnoid hemorrhage in monkeys.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 1996;16(4):688-97.
1996: Yamagata K; Takeda J; Menzel S; Chen X; Eng S; Lim L R; Concannon P; Hanis C L; Spielman R S; Cox N J; Bell G I
Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle.
Diabetologia 1996;39(6):725-30.
1996: Hanis C L; Boerwinkle E; Chakraborty R; Ellsworth D L; Concannon P; Stirling B; Morrison V A; Wapelhorst B; Spielman R S; Gogolin-Ewens K J; Shepard J M; Williams S R; Risch N; Hinds D; Iwasaki N; Ogata M; Omori Y; Petzold C; Rietzch H; Schröder H E; Schulze J; Cox N J; Menzel S; Boriraj V V; Chen X; Lim L R; Lindner T; Mereu L E; Wang Y Q; Xiang K; Yamagata K; Yang Y; Bell G I
A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.
Nature genetics 1996;13(2):161-6.
1996: Miller R J; Bell G I
JAK/STAT eats the fat.
Trends in neurosciences 1996;19(5):159-61.
1996: Stoffel M; Le Beau M M; Espinosa R; Bohlander S F; Le Paslier D; Cohen D; Xiang K S; Cox N J; Fajans S S; Bell G I
A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(9):3937-41.
1996: Tokuyama Y; Fan Z; Furuta H; Makielski J C; Polonsky K S; Bell G I; Yano H
Rat inwardly rectifying potassium channel Kir6.2: cloning electrophysiological characterization, and decreased expression in pancreatic islets of male Zucker diabetic fatty rats.
Biochemical and biophysical research communications 1996;220(3):532-8.
1996: Gambino V; Menzel S; Trabb J B; Xiang K S; Lindner T; Louït A; Chen E; Mereu L E; Furuta H; Iwasaki N; Kawamura M; Omori Y; Rietzsch H; Schulze J; Schröder H E; Concannon P; Hanis C L; Spielman R S; Yamagata K; Cox N J; Bell G I
An approach for identifying simple sequence repeat DNA polymorphisms near cloned cDNAs and genes. Linkage studies of the islet amyloid polypeptide/amylin and liver glycogen synthase genes and NIDDM.
Diabetes 1996;45(3):291-4.
1996: Iwasaki N; Kawamura M; Yamagata K; Cox N J; Karibe S; Ohgawara H; Inagaki N; Seino S; Bell G I; Omori Y
Identification of microsatellite markers near the human genes encoding the beta-cell ATP-sensitive K+ channel and linkage studies with NIDDM in Japanese.
Diabetes 1996;45(2):267-9.
1996: Roe M W; Worley J F; Tokuyama Y; Philipson L H; Sturis J; Tang J; Dukes I D; Bell G I; Polonsky K S
NIDDM is associated with loss of pancreatic beta-cell L-type Ca2+ channel activity.
The American journal of physiology 1996;270(1 Pt 1):E133-40.
1996: Bell G I; Pilkis S J; Weber I T; Polonsky K S
Glucokinase mutations, insulin secretion, and diabetes mellitus.
Annual review of physiology 1996;58():171-86.
1995: Stirling B; Cox N J; Bell G I; Hanis C L; Spielman R S; Concannon P
Linkage studies in NIDDM with markers near the sulphonylurea receptor gene.
Diabetologia 1995;38(12):1479-81.
1995: Tokuyama Y; Sturis J; DePaoli A M; Takeda J; Stoffel M; Tang J; Sun X; Polonsky K S; Bell G I
Evolution of beta-cell dysfunction in the male Zucker diabetic fatty rat.
Diabetes 1995;44(12):1447-57.
1995: Takeda J; Espinosa R; Eng S; Le Beau M M; Bell G I
Chromosomal assignment and tissue distribution of novel expressed sequence tags from a human pancreatic islet cDNA library.
Genomics 1995;29(1):276-81.
1995: Reisine T; Bell G I
Molecular biology of somatostatin receptors.
Endocrine reviews 1995;16(4):427-42.
1995: Reisine T; Bell G I
Molecular properties of somatostatin receptors.
Neuroscience 1995;67(4):777-90.
1995: Stirling B; Cox N J; Bell G I; Hanis C L; Spielman R S; Concannon P
Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs.
Diabetes 1995;44(8):999-1001.
1995: Stoffel M; Fernald A A; Le Beau M M; Bell G I
Assignment of the gastric inhibitory polypeptide receptor gene (GIPR) to chromosome bands 19q13.2-q13.3 by fluorescence in situ hybridization.
Genomics 1995;28(3):607-9.
1995: Stoffel M; Tokuyama Y; Trabb J B; German M S; Tsaar M L; Jan L Y; Polonsky K S; Bell G I
Cloning of rat KATP-2 channel and decreased expression in pancreatic islets of male Zucker diabetic fatty rats.
Biochemical and biophysical research communications 1995;212(3):894-9.
1995: Stoffel M; Stein R; Wright C V; Espinosa R; Le Beau M M; Bell G I
Localization of human homeodomain transcription factor insulin promoter factor 1 (IPF1) to chromosome band 13q12.1.
Genomics 1995;28(1):125-6.
1995: Byrne M M; Sturis J; Fajans S S; Ortiz F J; Stoltz A; Stoffel M; Smith M J; Bell G I; Halter J B; Polonsky K S
Altered insulin secretory responses to glucose in subjects with a mutation in the MODY1 gene on chromosome 20.
Diabetes 1995;44(6):699-704.
1995: Tokuyama Y; Hara M; Jones E M; Fan Z; Bell G I
Cloning of rat and mouse P2Y purinoceptors.
Biochemical and biophysical research communications 1995;211(1):211-8.
1995: Rowe R E; Wapelhorst B; Bell G I; Risch N; Spielman R S; Concannon P
Linkage and association between insulin-dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7.
Nature genetics 1995;10(2):240-2.
1995: el-Maghrabi M R; Lange A J; Jiang W; Yamagata K; Stoffel M; Takeda J; Fernald A A; Le Beau M M; Bell G I; Baker L
Human fructose-1,6-bisphosphatase gene (FBP1): exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiency.
Genomics 1995;27(3):520-5.
1995: Takeda J; Fernald A A; Yamagata K; Le Beau M M; Bell G I
Localization of human somatostatin receptor 5 gene (SSTR5) to chromosome band 16p13.3 by fluorescence in situ hybridization.
Genomics 1995;26(3):638-9.
1995: Iwasaki N; Ohgawara H; Nagahara H; Kawamura M; Bell G I; Omori Y
Characterization of Japanese families with early-onset type 2 (non-insulin dependent) diabetes mellitus and screening for mutations in the glucokinase and mitochondrial tRNA(Leu(UUR)) genes.
Acta diabetologica 1995;32(1):17-22.
1995: Wapelhorst B; Bell G I; Risch N; Spielman R S; Concannon P
Linkage and association studies in insulin-dependent diabetes with a new dinucleotide repeat polymorphism at the GAD65 locus.
Autoimmunity 1995;21(2):127-30.
1995: Bell G I; Yasuda K; Kong H; Law S F; Raynor K; Reisine T
Molecular biology of somatostatin receptors.
Ciba Foundation symposium 1995;190():65-79; discussion 80-8.
1995: Jones E M; Fernald A; Bell G I; Le Beau M M
Assignment of SLC6A9 to human chromosome band 1p33 by in situ hybridization.
Cytogenetics and cell genetics 1995;71(3):211.
1994: DePaoli A M; Bell G I; Stoffel M
G protein-activated inwardly rectifying potassium channel (GIRK1/KGA) mRNA in adult rat heart and brain by in situ hybridization histochemistry.
Molecular and cellular neurosciences 1994;5(6):515-22.
1994: Tallent M; Dichter M A; Bell G I; Reisine T
The cloned kappa opioid receptor couples to an N-type calcium current in undifferentiated PC-12 cells.
Neuroscience 1994;63(4):1033-40.
1994: Blondel O; Bell G I; Moody M; Miller R J; Gibbons S J
Creation of an inositol 1,4,5-trisphosphate-sensitive Ca2+ store in secretory granules of insulin-producing cells.
The Journal of biological chemistry 1994;269(44):27167-70.
1994: Stoffel M; Espinosa R; Trabb J B; Le Beau M M; Bell G I
Human type I pituitary adenylate cyclase activating polypeptide receptor (ADCYAP1R): localization to chromosome band 7p14 and integration into the cytogenetic, physical, and genetic map of chromosome 7.
Genomics 1994;23(3):697-9.
1994: Pilkis S J; Weber I T; Harrison R W; Bell G I
Glucokinase: structural analysis of a protein involved in susceptibility to diabetes.
The Journal of biological chemistry 1994;269(35):21925-8.
1994: Raynor K; Kong H; Hines J; Kong G; Benovic J; Yasuda K; Bell G I; Reisine T
Molecular mechanisms of agonist-induced desensitization of the cloned mouse kappa opioid receptor.
The Journal of pharmacology and experimental therapeutics 1994;270(3):1381-6.
1994: Jones E M; Menzel S; Espinosa R; Le Beau M M; Bell G I; Takeda J
Localization of the gene encoding a neutral amino acid transporter-like protein to human chromosome band 19q13.3 and characterization of a simple sequence repeat DNA polymorphism.
Genomics 1994;23(2):490-1.
1994: Kong H; Raynor K; Yano H; Takeda J; Bell G I; Reisine T
Agonists and antagonists bind to different domains of the cloned kappa opioid receptor.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(17):8042-6.
1994: Blondel O; Moody M M; Depaoli A M; Sharp A H; Ross C A; Swift H; Bell G I
Localization of inositol trisphosphate receptor subtype 3 to insulin and somatostatin secretory granules and regulation of expression in islets and insulinoma cells.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(16):7777-81.
1994: Theveniau M A; Yasuda K; Bell G I; Reisine T
Immunological detection of isoforms of the somatostatin receptor subtype, SSTR2.
Journal of neurochemistry 1994;63(2):447-55.
1994: Yano H; Philipson L H; Kugler J L; Tokuyama Y; Davis E M; Le Beau M M; Nelson D J; Bell G I; Takeda J
Alternative splicing of human inwardly rectifying K+ channel ROMK1 mRNA.
Molecular pharmacology 1994;45(5):854-60.
1994: Sturis J; Kurland I J; Byrne M M; Mosekilde E; Froguel P; Pilkis S J; Bell G I; Polonsky K S
Compensation in pancreatic beta-cell function in subjects with glucokinase mutations.
Diabetes 1994;43(5):718-23.
1994: Stoffel M; Espinosa R; Powell K L; Philipson L H; Le Beau M M; Bell G I
Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): localization to chromosome 2 and identification of a simple tandem repeat polymorphism.
Genomics 1994;21(1):254-6.
1994: Law S F; Zaina S; Sweet R; Yasuda K; Bell G I; Stadel J; Reisine T
Gi alpha 1 selectively couples somatostatin receptor subtype 3 to adenylyl cyclase: identification of the functional domains of this alpha subunit necessary for mediating the inhibition by somatostatin of cAMP formation.
Molecular pharmacology 1994;45(4):587-90.
1994: Kong H; DePaoli A M; Breder C D; Yasuda K; Bell G I; Reisine T
Differential expression of messenger RNAs for somatostatin receptor subtypes SSTR1, SSTR2 and SSTR3 in adult rat brain: analysis by RNA blotting and in situ hybridization histochemistry.
Neuroscience 1994;59(1):175-84.
1994: Byrne M M; Sturis J; Clément K; Vionnet N; Pueyo M E; Stoffel M; Takeda J; Passa P; Cohen D; Bell G I
Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations.
The Journal of clinical investigation 1994;93(3):1120-30.
1994: Menzel S; Stoffel M; Espinosa R; Fernald A A; Le Beau M M; Bell G I
Localization of the glucagon receptor gene to human chromosome band 17q25.
Genomics 1994;20(2):327-8.
1994: Yasuda K; Espinosa R; Takeda J; Le Beau M M; Bell G I
Localization of the kappa opioid receptor gene to human chromosome band 8q11.2.
Genomics 1994;19(3):596-7.
1994: Raynor K; Kong H; Chen Y; Yasuda K; Yu L; Bell G I; Reisine T
Pharmacological characterization of the cloned kappa-, delta-, and mu-opioid receptors.
Molecular pharmacology 1994;45(2):330-4.
1994: Takeda J; Blackburn C L; Menzel S; Yano H; Bell G I
Dinucleotide repeat polymorphism at D9S328E (EST hbc220).
Human molecular genetics 1994;3(2):387.
1993: Lehto M; Xiang K; Stoffel M; Espinosa R; Groop L C; Le Beau M M; Bell G I
Human hexokinase II: localization of the polymorphic gene to chromosome 2.
Diabetologia 1993;36(12):1299-302.
1993: Roulston D; Espinosa R; Stoffel M; Bell G I; Le Beau M M
Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20.
Blood 1993;82(11):3424-9.
1993: Reisine T; Bell G I
Molecular biology of opioid receptors.
Trends in neurosciences 1993;16(12):506-10.
1993: Seo T S; Hanabusa T; Ohagi S; Steiner D F; Bell G I
Dinucleotide repeat polymorphism in the NEC2 gene.
Human molecular genetics 1993;2(11):1983.
1993: Kong H; Raynor K; Yasuda K; Moe S T; Portoghese P S; Bell G I; Reisine T
A single residue, aspartic acid 95, in the delta opioid receptor specifies selective high affinity agonist binding.
The Journal of biological chemistry 1993;268(31):23055-8.
1993: Reisine T; Kong H; Raynor K; Yano H; Takeda J; Yasuda K; Bell G I
Splice variant of the somatostatin receptor 2 subtype, somatostatin receptor 2B, couples to adenylyl cyclase.
Molecular pharmacology 1993;44(5):1016-20.
1993: Takeda J; Yano H; Eng S; Zeng Y; Bell G I
A molecular inventory of human pancreatic islets: sequence analysis of 1000 cDNA clones.
Human molecular genetics 1993;2(11):1793-8.
1993: Bell G I; Burant C F; Takeda J; Gould G W
Structure and function of mammalian facilitative sugar transporters.
The Journal of biological chemistry 1993;268(26):19161-4.
1993: Yasuda K; Espinosa R; Davis E M; Le Beau M M; Bell G I
Human somatostatin receptor genes: localization of SSTR5 to human chromosome 20p11.2.
Genomics 1993;17(3):785-6.
1993: Stoffel M; Espinosa R; Le Beau M M; Bell G I
Human glucagon-like peptide-1 receptor gene. Localization to chromosome band 6p21 by fluorescence in situ hybridization and linkage of a highly polymorphic simple tandem repeat DNA polymorphism to other markers on chromosome 6.
Diabetes 1993;42(8):1215-8.
1993: Hayashi Y; Mori Y; Janssen O E; Sunthornthepvarakul T; Weiss R E; Takeda K; Weinberg M; Seo H; Bell G I; Refetoff S
Human thyroxine-binding globulin gene: complete sequence and transcriptional regulation.
Molecular endocrinology (Baltimore, Md.) 1993;7(8):1049-60.
1993: Raynor K; O'Carroll A M; Kong H; Yasuda K; Mahan L C; Bell G I; Reisine T
Characterization of cloned somatostatin receptors SSTR4 and SSTR5.
Molecular pharmacology 1993;44(2):385-92.
1993: Kong H; Raynor K; Yasuda K; Bell G I; Reisine T
Mutation of an aspartate at residue 89 in somatostatin receptor subtype 2 prevents Na+ regulation of agonist binding but does not alter receptor-G protein association.
Molecular pharmacology 1993;44(2):380-4.
1993: Yasuda K; Raynor K; Kong H; Breder C D; Takeda J; Reisine T; Bell G I
Cloning and functional comparison of kappa and delta opioid receptors from mouse brain.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(14):6736-40.
1993: Iwashima Y; Pugh W; Depaoli A M; Takeda J; Seino S; Bell G I; Polonsky K S
Expression of calcium channel mRNAs in rat pancreatic islets and downregulation after glucose infusion.
Diabetes 1993;42(7):948-55.
1993: Vionnet N; Bell G I
Identification of a simple tandem repeat DNA polymorphism in the human glycogen synthase gene and linkage to five markers on chromosome 19q.
Diabetes 1993;42(6):930-2.
1993: Rand E B; Depaoli A M; Davidson N O; Bell G I; Burant C F
Sequence, tissue distribution, and functional characterization of the rat fructose transporter GLUT5.
The American journal of physiology 1993;264(6 Pt 1):G1169-76.
1993: Raynor K; Murphy W A; Coy D H; Taylor J E; Moreau J P; Yasuda K; Bell G I; Reisine T
Cloned somatostatin receptors: identification of subtype-selective peptides and demonstration of high affinity binding of linear peptides.
Molecular pharmacology 1993;43(6):838-44.
1993: Olson A L; Liu M L; Moye-Rowley W S; Buse J B; Bell G I; Pessin J E
Hormonal/metabolic regulation of the human GLUT4/muscle-fat facilitative glucose transporter gene in transgenic mice.
The Journal of biological chemistry 1993;268(13):9839-46.
1993: Blondel O; Takeda J; Janssen H; Seino S; Bell G I
Sequence and functional characterization of a third inositol trisphosphate receptor subtype, IP3R-3, expressed in pancreatic islets, kidney, gastrointestinal tract, and other tissues.
The Journal of biological chemistry 1993;268(15):11356-63.
1993: Law S F; Yasuda K; Bell G I; Reisine T
Gi alpha 3 and G(o) alpha selectively associate with the cloned somatostatin receptor subtype SSTR2.
The Journal of biological chemistry 1993;268(15):10721-7.
1993: Stoffel M; Espinosa R; Keller S R; Lienhard G E; Le Beau M M; Bell G I
Human insulin receptor substrate-1 gene (IRS1): chromosomal localization to 2q35-q36.1 and identification of a simple tandem repeat DNA polymorphism.
Diabetologia 1993;36(4):335-7.
1993: Stoffel M; Bell G I
Characterization of a third simple tandem repeat polymorphism in the human glucokinase gene.
Diabetologia 1993;36(2):170-1.
1993: Philipson L H; Eddy R L; Shows T B; Bell G I
Assignment of human potassium channel gene KCNA4 (Kv1.4, PCN2) to chromosome 11q13.4-->q14.1.
Genomics 1993;15(2):463-4.
1993: Lehto M; Stoffel M; Groop L; Espinosa R; Le Beau M M; Bell G I
Assignment of the gene encoding glycogen synthase (GYS) to human chromosome 19, band q13.3.
Genomics 1993;15(2):460-1.
1993: Yamada Y; Stoffel M; Espinosa R; Xiang K S; Seino M; Seino S; Le Beau M M; Bell G I
Human somatostatin receptor genes: localization to human chromosomes 14, 17, and 22 and identification of simple tandem repeat polymorphisms.
Genomics 1993;15(2):449-52.
1993: Stoffel M; Xiang K S; Espinosa R; Cox N J; Le Beau M M; Bell G I
cDNA sequence and localization of polymorphic human cytosolic phosphoenolpyruvate carboxykinase gene (PCK1) to chromosome 20, band q13.31: PCK1 is not tightly linked to maturity-onset diabetes of the young.
Human molecular genetics 1993;2(1):1-4.
1993: Bell G I; Reisine T
Molecular biology of somatostatin receptors.
Trends in neurosciences 1993;16(1):34-8.
1992: Yamada Y; Reisine T; Law S F; Ihara Y; Kubota A; Kagimoto S; Seino M; Seino Y; Bell G I; Seino S
Somatostatin receptors, an expanding gene family: cloning and functional characterization of human SSTR3, a protein coupled to adenylyl cyclase.
Molecular endocrinology (Baltimore, Md.) 1992;6(12):2136-42.
1992: Buse J B; Yasuda K; Lay T P; Seo T S; Olson A L; Pessin J E; Karam J H; Seino S; Bell G I
Human GLUT4/muscle-fat glucose-transporter gene. Characterization and genetic variation.
Diabetes 1992;41(11):1436-45.
1992: Stoffel M; Xiang K; Bell G I
Dinucleotide repeat polymorphism at the human ribophorin II locus (RPN2) on chromosome 20q.
Human molecular genetics 1992;1(8):656.
1992: Burant C F; Bell G I
Mammalian facilitative glucose transporters: evidence for similar substrate recognition sites in functionally monomeric proteins.
Biochemistry 1992;31(42):10414-20.
1992: Breder C D; Yamada Y; Yasuda K; Seino S; Saper C B; Bell G I
Differential expression of somatostatin receptor subtypes in brain.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1992;12(10):3920-34.
1992: Yasuda K; Rens-Domiano S; Breder C D; Law S F; Saper C B; Reisine T; Bell G I
Cloning of a novel somatostatin receptor, SSTR3, coupled to adenylylcyclase.
The Journal of biological chemistry 1992;267(28):20422-8.
1992: Sakurai A; Bell G I; DeGroot L J
Dinucleotide repeat polymorphism in the human thyroid hormone receptor alpha gene (THRA1) on chromosome 17.
Human molecular genetics 1992;1(7):553.
1992: Stoffel M; Patel P; Lo Y M; Hattersley A T; Lucassen A M; Page R; Bell J I; Bell G I; Turner R C; Wainscoat J S
Missense glucokinase mutation in maturity-onset diabetes of the young and mutation screening in late-onset diabetes.
Nature genetics 1992;2(2):153-6.
1992: Murray J C; Bennett S R; Kwitek A E; Small K W; Schinzel A; Alward W L; Weber J L; Bell G I; Buetow K H
Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4.
Nature genetics 1992;2(1):46-9.
1992: Nishi S; Stoffel M; Xiang K; Shows T B; Bell G I; Takeda J
Human pancreatic beta-cell glucokinase: cDNA sequence and localization of the polymorphic gene to chromosome 7, band p 13.
Diabetologia 1992;35(8):743-7.
1992: Seino S; Yamada Y; Espinosa R; Le Beau M M; Bell G I
Assignment of the gene encoding the alpha 1 subunit of the neuroendocrine/brain-type calcium channel (CACNL1A2) to human chromosome 3, band p14.3.
Genomics 1992;13(4):1375-7.
1992: Burant C F; Takeda J; Brot-Laroche E; Bell G I; Davidson N O
Fructose transporter in human spermatozoa and small intestine is GLUT5.
The Journal of biological chemistry 1992;267(21):14523-6.
1992: Rens-Domiano S; Law S F; Yamada Y; Seino S; Bell G I; Reisine T
Pharmacological properties of two cloned somatostatin receptors.
Molecular pharmacology 1992;42(1):28-34.
1992: Drummond I A; Madden S L; Rohwer-Nutter P; Bell G I; Sukhatme V P; Rauscher F J
Repression of the insulin-like growth factor II gene by the Wilms tumor suppressor WT1.
Science (New York, N.Y.) 1992;257(5070):674-8.
1992: Liu M L; Olson A L; Moye-Rowley W S; Buse J B; Bell G I; Pessin J E
Expression and regulation of the human GLUT4/muscle-fat facilitative glucose transporter gene in transgenic mice.
The Journal of biological chemistry 1992;267(17):11673-6.
1992: Cox N J; Xiang K S; Fajans S S; Bell G I
Mapping diabetes-susceptibility genes. Lessons learned from search for DNA marker for maturity-onset diabetes of the young.
Diabetes 1992;41(4):401-7.
1992: Vionnet N; Stoffel M; Takeda J; Yasuda K; Bell G I; Zouali H; Lesage S; Velho G; Iris F; Passa P
Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus.
Nature 1992;356(6371):721-2.
1992: Seino S; Bell G I; Li W H
Sequences of primate insulin genes support the hypothesis of a slower rate of molecular evolution in humans and apes than in monkeys.
Molecular biology and evolution 1992;9(2):193-203.
1992: Davidson N O; Hausman A M; Ifkovits C A; Buse J B; Gould G W; Burant C F; Bell G I
Human intestinal glucose transporter expression and localization of GLUT5.
The American journal of physiology 1992;262(3 Pt 1):C795-800.
1992: Stoffel M; Bell G I
Microsatellite polymorphism in the human platelet glycoprotein IIIa gene (GP3A) on chromosome 17.
Nucleic acids research 1992;20(5):1172.
1992: Nagamatsu S; Kornhauser J M; Burant C F; Seino S; Mayo K E; Bell G I
Glucose transporter expression in brain. cDNA sequence of mouse GLUT3, the brain facilitative glucose transporter isoform, and identification of sites of expression by in situ hybridization.
The Journal of biological chemistry 1992;267(1):467-72.
1992: Yamada Y; Post S R; Wang K; Tager H S; Bell G I; Seino S
Cloning and functional characterization of a family of human and mouse somatostatin receptors expressed in brain, gastrointestinal tract, and kidney.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(1):251-5.
1992: Seino S; Chen L; Seino M; Blondel O; Takeda J; Johnson J H; Bell G I
Cloning of the alpha 1 subunit of a voltage-dependent calcium channel expressed in pancreatic beta cells.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(2):584-8.
1992: Pessin J E; Bell G I
Mammalian facilitative glucose transporter family: structure and molecular regulation.
Annual review of physiology 1992;54():911-30.
1991: Iwasaki N; Xiang K; Seino M; Bell G I
Dinucleotide repeat polymorphism in D20S17 (CRI-L127).
Nucleic acids research 1991;19(24):6970.
1991: Xiang K; Phillippe G; Seino M; Bonham K; Fugita D J; Bell G I
Dinucleotide repeat polymorphism in the human SRC gene on chromosome 20.
Nucleic acids research 1991;19(24):6967.
1991: Sakurai A; Bell G I; DeGroot L J
Dinucleotide repeat polymorphism in the human thyroid hormone receptor beta gene (THRB) on chromosome 3.
Nucleic acids research 1991;19(23):6661.
1991: Xiang K; Granqvist M; Seino M; Seino S; Bell G I
Microsatellite polymorphism in human insulin receptor gene (INSR) on chromosome 19.
Nucleic acids research 1991;19(18):5094.
1991: Granqvist M; Xiang K; Seino M; Fukumoto H; Bell G I
Dinucleotide repeat polymorphism in human GLUT2/liver facilitative glucose transporter gene on chromosome 3.
Nucleic acids research 1991;19(17):4791.
1991: Granqvist M; Xiang K; Seino M; Bell G I
Dinucleotide repeat polymorphism in Gs-alpha subunit gene (GNAS1) on chromosome 20.
Nucleic acids research 1991;19(16):4569.
1991: Ohagi S; Nishi M; Bell G I; Ensinck J W; Steiner D F
Sequences of islet amyloid polypeptide precursors of an Old World monkey, the pig-tailed macaque (Macaca nemestrina), and the dog (Canis familiaris).
Diabetologia 1991;34(8):555-8.
1991: Yamada Y; Xiang K S; Bell G I; Seino S; Nishi M
Dinucleotide repeat polymorphism in a gene on chromosome 20 encoding a G-protein coupled receptor (D20S32e).
Nucleic acids research 1991;19(9):2519.
1991: Bell G I
Lilly lecture 1990. Molecular defects in diabetes mellitus.
Diabetes 1991;40(4):413-22.
1991: Wu S; Xiang K; Bell G I
Dinucleotide repeat polymorphism in the human glucagon gene (GCG).
Nucleic acids research 1991;19(5):1163.
1991: Steiner D F; Ohagi S; Nagamatsu S; Bell G I; Nishi M
Is islet amyloid polypeptide a significant factor in pathogenesis or pathophysiology of diabetes?
Diabetes 1991;40(3):305-9.
1991: Bell G I; Xiang K S; Newman M V; Wu S H; Wright L G; Fajans S S; Spielman R S; Cox N J
Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(4):1484-8.
1991: Philipson L H; Hice R E; Schaefer K; LaMendola J; Bell G I; Nelson D J; Steiner D F
Sequence and functional expression in Xenopus oocytes of a human insulinoma and islet potassium channel.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(1):53-7.
1991: Burant C F; Sivitz W I; Fukumoto H; Kayano T; Nagamatsu S; Seino S; Pessin J E; Bell G I
Mammalian glucose transporters: structure and molecular regulation.
Recent progress in hormone research 1991;47():349-87; discussion 387-8.
1990: Philipson L H; Schaefer K; LaMendola J; Bell G I; Steiner D F
Sequence of a human fetal skeletal muscle potassium channel cDNA related to RCK4.
Nucleic acids research 1990;18(23):7160.
1990: Nishi M; Bell G I; Steiner D F
Sequence of a cDNA encoding Syrian hamster islet amyloid polypeptide precursor.
Nucleic acids research 1990;18(22):6726.
1990: Becker M A; Heidler S A; Bell G I; Seino S; Le Beau M M; Westbrook C A; Neuman W; Shapiro L J; Mohandas T K; Roessler B J
Cloning of cDNAs for human phosphoribosylpyrophosphate synthetases 1 and 2 and X chromosome localization of PRPS1 and PRPS2 genes.
Genomics 1990;8(3):555-61.
1990: Nishi M; Bell G I; Steiner D F
Islet amyloid polypeptide (amylin): no evidence of an abnormal precursor sequence in 25 type 2 (non-insulin-dependent) diabetic patients.
Diabetologia 1990;33(10):628-30.
1990: Kayano T; Burant C F; Fukumoto H; Gould G W; Fan Y S; Eddy R L; Byers M G; Shows T B; Seino S; Bell G I
Human facilitative glucose transporters. Isolation, functional characterization, and gene localization of cDNAs encoding an isoform (GLUT5) expressed in small intestine, kidney, muscle, and adipose tissue and an unusual glucose transporter pseudogene-like sequence (GLUT6).
The Journal of biological chemistry 1990;265(22):13276-82.
1990: Shapiro E T; Bell G I; Polonsky K S; Rubenstein A H; Kew M C; Tager H S
Tumor hypoglycemia: relationship to high molecular weight insulin-like growth factor-II.
The Journal of clinical investigation 1990;85(5):1672-9.
1990: Wu S; Seino S; Bell G I
Human collagen, type II, alpha 1, (COL2A1) gene: VNTR polymorphism detected by gene amplification.
Nucleic acids research 1990;18(10):3102.
1990: Sivitz W I; DeSautel S L; Kayano T; Bell G I; Pessin J E
Regulation of glucose transporter messenger RNA levels in rat adipose tissue by insulin.
Molecular endocrinology (Baltimore, Md.) 1990;4(4):583-8.
1990: Nishi M; Sanke T; Nagamatsu S; Bell G I; Steiner D F
Islet amyloid polypeptide. A new beta cell secretory product related to islet amyloid deposits.
The Journal of biological chemistry 1990;265(8):4173-6.
1990: Bell G I; Kayano T; Buse J B; Burant C F; Takeda J; Lin D; Fukumoto H; Seino S
Molecular biology of mammalian glucose transporters.
Diabetes care 1990;13(3):198-208.
1990: Seino S; Seino M; Bell G I
Human insulin-receptor gene.
Diabetes 1990;39(2):129-33.
1990: Seino S; Seino M; Bell G I
Human insulin-receptor gene. Partial sequence and amplification of exons by polymerase chain reaction.
Diabetes 1990;39(1):123-8.
1989: Nishi M; Sanke T; Seino S; Eddy R L; Fan Y S; Byers M G; Shows T B; Bell G I; Steiner D F
Human islet amyloid polypeptide gene: complete nucleotide sequence, chromosomal localization, and evolutionary history.
Molecular endocrinology (Baltimore, Md.) 1989;3(11):1775-81.
1989: Sakurai A; Takeda K; Ain K; Ceccarelli P; Nakai A; Seino S; Bell G I; Refetoff S; DeGroot L J
Generalized resistance to thyroid hormone associated with a mutation in the ligand-binding domain of the human thyroid hormone receptor beta.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(22):8977-81.
1989: Nishi S; Newman M; Bell G I
HincII RFLP at the human hexokinase I (HK1) locus on chromosome 10.
Nucleic acids research 1989;17(18):7547.
1989: Ardinger H H; Buetow K H; Bell G I; Bardach J; VanDemark D R; Murray J C
Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate.
American journal of human genetics 1989;45(3):348-53.
1989: Wu S; Seino S; Bell G I
Human antithrombin II (AT3) gene length polymorphism revealed by the polymerase chain reaction.
Nucleic acids research 1989;17(15):6433.
1989: Nishi M; Chan S J; Nagamatsu S; Bell G I; Steiner D F
Conservation of the sequence of islet amyloid polypeptide in five mammals is consistent with its putative role as an islet hormone.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(15):5738-42.
1989: Cox N J; Bell G I
Disease associations. Chance, artifact, or susceptibility genes?
Diabetes 1989;38(8):947-50.
1989: Bell G I; Murray J C; Nakamura Y; Kayano T; Eddy R L; Fan Y S; Byers M G; Shows T B
Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13.
Diabetes 1989;38(8):1072-5.
1989: Sivitz W I; DeSautel S L; Kayano T; Bell G I; Pessin J E
Regulation of glucose transporter messenger RNA in insulin-deficient states.
Nature 1989;340(6228):72-4.
1989: Inagaki N; Seino Y; Takeda J; Yano H; Yamada Y; Bell G I; Eddy R L; Fukushima Y; Byers M G; Shows T B
Gastric inhibitory polypeptide: structure and chromosomal localization of the human gene.
Molecular endocrinology (Baltimore, Md.) 1989;3(6):1014-21.
1989: Yano H; Seino Y; Fujita J; Yamada Y; Inagaki N; Takeda J; Bell G I; Eddy R L; Fan Y S; Byers M G
Exon-intron organization, expression, and chromosomal localization of the human motilin gene.
FEBS letters 1989;249(2):248-52.
1989: Fukumoto H; Kayano T; Buse J B; Edwards Y; Pilch P F; Bell G I; Seino S
Cloning and characterization of the major insulin-responsive glucose transporter expressed in human skeletal muscle and other insulin-responsive tissues.
The Journal of biological chemistry 1989;264(14):7776-9.
1989: Leysens N; Murray J C; Bell G I
A KpnI polymorphism for the human insulin-responsive glucose transporter gene (GLUT4) on chromosome 17.
Nucleic acids research 1989;17(9):3621.
1989: Takeda K; Mori Y; Sobieszczyk S; Seo H; Dick M; Watson F; Flink I L; Seino S; Bell G I; Refetoff S
Sequence of the variant thyroxine-binding globulin of Australian aborigines. Only one of two amino acid replacements is responsible for its altered properties.
The Journal of clinical investigation 1989;83(4):1344-8.
1989: Mori Y; Seino S; Takeda K; Flink I L; Murata Y; Bell G I; Refetoff S
A mutation causing reduced biological activity and stability of thyroxine-binding globulin probably as a result of abnormal glycosylation of the molecule.
Molecular endocrinology (Baltimore, Md.) 1989;3(3):575-9.
1989: Seino S; Bell G I
Alternative splicing of human insulin receptor messenger RNA.
Biochemical and biophysical research communications 1989;159(1):312-6.
1989: Xiang K S; Cox N J; Sanz N; Huang P; Karam J H; Bell G I
Insulin-receptor and apolipoprotein genes contribute to development of NIDDM in Chinese Americans.
Diabetes 1989;38(1):17-23.
1988: Nishi S; Seino S; Bell G I
Human hexokinase: sequences of amino- and carboxyl-terminal halves are homologous.
Biochemical and biophysical research communications 1988;157(3):937-43.
1988: Sanke T; Bell G I; Sample C; Rubenstein A H; Steiner D F
An islet amyloid peptide is derived from an 89-amino acid precursor by proteolytic processing.
The Journal of biological chemistry 1988;263(33):17243-6.
1988: Nakai A; Sakurai A; Bell G I; DeGroot L J
Characterization of a third human thyroid hormone receptor coexpressed with other thyroid hormone receptors in several tissues.
Molecular endocrinology (Baltimore, Md.) 1988;2(11):1087-92.
1988: Kayano T; Fukumoto H; Eddy R L; Fan Y S; Byers M G; Shows T B; Bell G I
Evidence for a family of human glucose transporter-like proteins. Sequence and gene localization of a protein expressed in fetal skeletal muscle and other tissues.
The Journal of biological chemistry 1988;263(30):15245-8.
1988: Cox N J; Bell G I; Xiang K S
Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II.
American journal of human genetics 1988;43(4):495-501.
1988: Ardinger H H; Ardinger R H; Bell G I; Murray J C
RFLP for the human transforming growth factor beta-1 gene (TGFB) on chromosome 19.
Nucleic acids research 1988;16(16):8202.
1988: Seino S; Blackstone C D; Chan S J; Whittaker J; Bell G I; Steiner D F
Appalachian spring: variations on ancient gastro-entero-pancreatic themes in New World mammals.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 1988;20(7):430-5.
1988: Yoshimasa Y; Seino S; Whittaker J; Kakehi T; Kosaki A; Kuzuya H; Imura H; Bell G I; Steiner D F
Insulin-resistant diabetes due to a point mutation that prevents insulin proreceptor processing.
Science (New York, N.Y.) 1988;240(4853):784-7.
1988: Fukumoto H; Seino S; Imura H; Seino Y; Bell G I
Characterization and expression of human HepG2/erythrocyte glucose-transporter gene.
Diabetes 1988;37(5):657-61.
1988: McCreary V; Kartha S; Bell G I; Toback F G
Sequence of a human kidney cDNA clone encoding thymosin beta 10.
Biochemical and biophysical research communications 1988;152(2):862-6.
1988: Nakai A; Seino S; Sakurai A; Szilak I; Bell G I; DeGroot L J
Characterization of a thyroid hormone receptor expressed in human kidney and other tissues.
Proceedings of the National Academy of Sciences of the United States of America 1988;85(8):2781-5.
1988: Xiang K; Cox N J; Bell G I
Apa I and Sst I RFLPs at the insulin-like growth factor II (IGF2) locus on chromosome 11.
Nucleic acids research 1988;16(8):3599.
1987: Seino S; Steiner D F; Bell G I
Sequence of a New World primate insulin having low biological potency and immunoreactivity.
Proceedings of the National Academy of Sciences of the United States of America 1987;84(21):7423-7.
1987: Xiang K; Cox N J; Karam J H; Bell G I
Bgl II RFLP at the human erythrocyte/HepG2-type glucose transporter (GLUT) locus on chromosome 1.
Nucleic acids research 1987;15(21):9101.
1987: Xiang K; Karam J H; Bell G I
BamHI RFLP at the insulin-like growth factor II (IGF2) locus on chromosome 11.
Nucleic acids research 1987;15(18):7655.
1987: Xiang K; Cox N J; Hallewell R A; Bell G I
Multiple Taq I RFLPs at the human manganese superoxide dismutase (S0D2) locus on chromosome 6.
Nucleic acids research 1987;15(18):7654.
1987: Bell G I; Xiang K; Horita S; Sanz N; Karam J H
The molecular genetics of diabetes mellitus.
Ciba Foundation symposium 1987;130():167-83.
1985: Elbein S; Rotwein P; Permutt M A; Bell G I; Sanz N; Karam J H
Lack of association of the polymorphic locus in the 5'-flanking region of the human insulin gene and diabetes in American blacks.
Diabetes 1985;34(5):433-9.

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