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Mitsuru Emi

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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Disorders

Genes & Molecular Sequences

Procedures

Chemicals & Drugs

Geographic Areas

Japan

Concepts & Ideas

Phenomena

Single-Stranded Conformational Polymorphism

Physiology

Genotype

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Co-Publications
Name
40
Nagai, Hisaki
31
Nakajima, Toshiaki
27
Ezura, Yoichi
22
Kasumi, Fujio
21
Sakamoto, Goi
20
Nakamura, Yusuke
19
Onda, Masamitsu
16
Lalouel, Jean-Marc
16
Kajita, Mitsuko
14
Hosoi, Takayuki
14
Harada, Haruhito
14
Suzuki, Takao
13
Wu, Lily
13
Hopkins, Paul
13
Iwasaki, Hironori

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Publications

TOP 3
Mii Akiko; Nakajima Toshiaki; Fujita Yuko; Iino Yasuhiko; Kamimura Kouhei; Bujo Hideaki; Saito Yasushi; Emi Mitsuru; Katayama Yasuo
Genetic association of low-density lipoprotein receptor-related protein 2 (LRP2) with plasma lipid levels.
Ezura Yoichi; Nakajima Toshiaki; Urano Tomohiko; Sudo Yoshihiro; Kajita Mitsuko; Yoshida Hideyo; Suzuki Takao; Hosoi Takayuki; Inoue Satoshi; Shiraki Masataka; Emi Mitsuru
Association of a single-nucleotide variation (A1330V) in the low-density lipoprotein receptor-related protein 5 gene (LRP5) with bone mineral density in adult Japanese women.
Ishijima Muneaki; Ezura Yoichi; Tsuji Kunikazu; Rittling Susan R; Kurosawa Hisashi; Denhardt David T; Emi Mitsuru; Nifuji Akira; Noda Masaki
Osteopontin is associated with nuclear factor kappaB gene expression during tail-suspension-induced bone loss.

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All Publications

2007: Mii Akiko; Nakajima Toshiaki; Fujita Yuko; Iino Yasuhiko; Kamimura Kouhei; Bujo Hideaki; Saito Yasushi; Emi Mitsuru; Katayama Yasuo
Genetic association of low-density lipoprotein receptor-related protein 2 (LRP2) with plasma lipid levels.
Journal of atherosclerosis and thrombosis 2007;14(6):310-6.
2007: Ezura Yoichi; Nakajima Toshiaki; Urano Tomohiko; Sudo Yoshihiro; Kajita Mitsuko; Yoshida Hideyo; Suzuki Takao; Hosoi Takayuki; Inoue Satoshi; Shiraki Masataka; Emi Mitsuru
Association of a single-nucleotide variation (A1330V) in the low-density lipoprotein receptor-related protein 5 gene (LRP5) with bone mineral density in adult Japanese women.
Bone 2007;40(4):997-1005.
2006: Ishijima Muneaki; Ezura Yoichi; Tsuji Kunikazu; Rittling Susan R; Kurosawa Hisashi; Denhardt David T; Emi Mitsuru; Nifuji Akira; Noda Masaki
Osteopontin is associated with nuclear factor kappaB gene expression during tail-suspension-induced bone loss.
Experimental cell research 2006;312(16):3075-83.
2005: Mizutani Kazunori; Miyamoto Shizuyo; Nagahata Takemitsu; Konishi Noboru; Emi Mitsuru; Onda Masamitsu
Upregulation and overexpression of DVL1, the human counterpart of the Drosophila dishevelled gene, in prostate cancer.
Tumori 2005;91(6):546-51.
2005: Nakajima T; Wooding S; Satta Y; Jinnai N; Goto S; Hayasaka I; Saitou N; Guan-Jun J; Tokunaga K; Jorde L B; Emi M; Inoue I
Evidence for natural selection in the HAVCR1 gene: high degree of amino-acid variability in the mucin domain of human HAVCR1 protein.
Genes and immunity 2005;6(5):398-406.
2005: Onda M; Akaishi J; Asaka S; Okamoto J; Miyamoto S; Mizutani K; Yoshida A; Ito K; Emi M
Decreased expression of haemoglobin beta (HBB) gene in anaplastic thyroid cancer and recovery of its expression inhibits cell growth.
British journal of cancer 2005;92(12):2216-24.
2005: Mizutani Kazunori; Onda Masamitsu; Asaka Shinichi; Akaishi Junko; Miyamoto Shizuyo; Yoshida Akira; Nagahama Mitsuji; Ito Kouichi; Emi Mitsuru
Overexpressed in anaplastic thyroid carcinoma-1 (OEATC-1) as a novel gene responsible for anaplastic thyroid carcinoma.
Cancer 2005;103(9):1785-90.
2005: Nagahata T; Sato T; Tomura A; Onda M; Nishikawa K; Emi M
Identification of RAI3 as a therapeutic target for breast cancer.
Endocrine-related cancer 2005;12(1):65-73.
2005: Shioji Go; Ezura Yoichi; Nakajima Toshiaki; Ohgaki Kenji; Fujiwara Hiromichi; Kubota Yoshinobu; Ichikawa Tomohiko; Inoue Katsuki; Shuin Taro; Habuchi Tomonori; Ogawa Osamu; Nishimura Taiji; Emi Mitsuru
Nucleotide variations in genes encoding plasminogen activator inhibitor-2 and serine proteinase inhibitor B10 associated with prostate cancer.
Journal of human genetics 2005;50(10):507-15.
2005: Sudo Yoshihiro; Ezura Yoichi; Kajita Mitsuko; Yoshida Hideyo; Suzuki Takao; Hosoi Takayuki; Inoue Satoshi; Shiraki Masataka; Ito Hiromoto; Emi Mitsuru
Association of single nucleotide polymorphisms in the promoter region of the pro-opiomelanocortin gene (POMC) with low bone mineral density in adult women.
Journal of human genetics 2005;50(5):235-40.
2005: Fujita Yuko; Ezura Yoichi; Bujo Hideaki; Nakajima Toshiaki; Takahashi Kaneo; Kamimura Kouhei; Iino Yasuhiko; Katayama Yasuo; Saito Yasushi; Emi Mitsuru
Association of nucleotide variations in the apolipoprotein B48 receptor gene (APOB48R) with hypercholesterolemia.
Journal of human genetics 2005;50(4):203-9.
2004: Kouno Jun; Nagai Hisaki; Nagahata Takemitsu; Onda Masamitsu; Yamaguchi Humio; Adachi Koji; Takahashi Hiroshi; Teramoto Akira; Emi Mitsuru
Up-regulation of CC chemokine, CCL3L1, and receptors, CCR3, CCR5 in human glioblastoma that promotes cell growth.
Journal of neuro-oncology 2004;70(3):301-7.
2004: Onda M; Emi M; Yoshida A; Miyamoto S; Akaishi J; Asaka S; Mizutani K; Shimizu K; Nagahama M; Ito K; Tanaka T; Tsunoda T
Comprehensive gene expression profiling of anaplastic thyroid cancers with cDNA microarray of 25 344 genes.
Endocrine-related cancer 2004;11(4):843-54.
2004: Onda Masamitsu; Emi Mitsuru; Nagai Hisaki; Nagahata Takemitsu; Tsumagari Kouji; Fujimoto Takashi; Akiyama Futoshi; Sakamoto Goi; Makita Masujirou; Kasumi Fujio; Miki Yoshio; Tanaka Toshihiro; Tsunoda Tatsuhiko; Nakamura Yusuke
Gene expression patterns as marker for 5-year postoperative prognosis of primary breast cancers.
Journal of cancer research and clinical oncology 2004;130(9):537-45.
2004: Ezura Yoichi; Kajita Mitsuko; Ishida Ryota; Yoshida Shoko; Yoshida Hideyo; Suzuki Takao; Hosoi Takayuki; Inoue Satoshi; Shiraki Masataka; Orimo Hajime; Emi Mitsuru
Association of multiple nucleotide variations in the pituitary glutaminyl cyclase gene (QPCT) with low radial BMD in adult women.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2004;19(8):1296-301.
2004: Nakajima Toshiaki; Wooding Stephen; Sakagami Takuro; Emi Mitsuru; Tokunaga Katsushi; Tamiya Gen; Ishigami Tomoaki; Umemura Satoshi; Munkhbat Batmunkh; Jin Feng; Guan-Jun Jia; Hayasaka Ikuo; Ishida Takafumi; Saitou Naruya; Pavelka Karel; Lalouel Jean-Marc; Jorde Lynn B; Inoue Ituro
Natural selection and population history in the human angiotensinogen gene (AGT): 736 complete AGT sequences in chromosomes from around the world.
American journal of human genetics 2004;74(5):898-916.
2004: Komazaki Toshiaki; Nagai Hisaki; Emi Mitsuru; Terada Yoshie; Yabe Aya; Jin Enjing; Kawanami Ooiti; Konishi Noboru; Moriyama Yukichi; Naka Tetsuji; Kishimoto Tadamitsu
Hypermethylation-associated inactivation of the SOCS-1 gene, a JAK/STAT inhibitor, in human pancreatic cancers.
Japanese journal of clinical oncology 2004;34(4):191-4.
2004: Nagahata Takemitsu; Onda Masamitsu; Emi Mitsuru; Nagai Hisaki; Tsumagari Koji; Fujimoto Takashi; Hirano Akira; Sato Takamichi; Nishikawa Kiyohiro; Akiyama Futoshi; Sakamoto Goi; Kasumi Fujio; Miki Yoshio; Tanaka Toshihiro; Tsunoda Tatsuhiko
Expression profiling to predict postoperative prognosis for estrogen receptor-negative breast cancers by analysis of 25,344 genes on a cDNA microarray.
Cancer science 2004;95(3):218-25.
2004: Hatta Mitsuko; Nagai Hisaki; Okino Keiko; Onda Masamitsu; Yoneyama Koichi; Ohta Yujirou; Nakayama Hiroki; Araki Tsutomu; Emi Mitsuru
Down-regulation of members of glycolipid-enriched membrane raft gene family, MAL and BENE, in cervical squamous cell cancers.
The journal of obstetrics and gynaecology research 2004;30(1):53-8.
2004: Iwasaki Tadao; Takahashi Sadao; Ishihara Mitsuaki; Takahashi Masafumi; Ikeda Uichi; Shimada Kazuyuki; Fujino Takahiro; Yamamoto Tokuo T; Hattori Hiroaki; Emi Mitsuru
The important role for betaVLDLs binding at the fourth cysteine of first ligand-binding domain in the low-density lipoprotein receptor.
Journal of human genetics 2004;49(11):622-8.
2004: Nagai Hisaki; Terada Yoshie; Tajiri Takashi; Yabe Aya; Onda Masamitsu; Nagahata Takemitsu; Ezura Yoichi; Minegishi Masaharu; Horiguchi Maya; Baba Masaru; Konishi Noboru; Emi Mitsuru
Characterization of liver-cirrhosis nodules by analysis of gene-expression profiles and patterns of allelic loss.
Journal of human genetics 2004;49(5):246-55.
2004: Urano Tomohiko; Shiraki Masataka; Ezura Yoichi; Fujita Masayo; Sekine Emiko; Hoshino Shinjiro; Hosoi Takayuki; Orimo Hajime; Emi Mitsuru; Ouchi Yasuyoshi; Inoue Satoshi
Association of a single-nucleotide polymorphism in low-density lipoprotein receptor-related protein 5 gene with bone mineral density.
Journal of bone and mineral metabolism 2004;22(4):341-5.
2004: Ishihara Mitsuaki; Iwasaki Tadao; Nagano Makoto; Ishii Jun; Takano Mayumi; Kujiraoka Takeshi; Tsuji Masahiro; Hattori Hiroaki; Emi Mitsuru
Functional impairment of two novel mutations detected in lipoprotein-associated phospholipase A2 (Lp-PLA2) deficiency patients.
Journal of human genetics 2004;49(6):302-7.
2004: Hirata Tomomi; Nagai Hisaki; Koizumi Kiyoshi; Okino Keiko; Harada Akima; Onda Masamitsu; Nagahata Takemitsu; Mikami Iwao; Hirai Kyoji; Haraguchi Syuji; Jin Enjing; Kawanami Oichi; Shimizu Kazuo; Emi Mitsuru
Amplification, up-regulation and over-expression of C3G (CRK SH3 domain-binding guanine nucleotide-releasing factor) in non-small cell lung cancers.
Journal of human genetics 2004;49(6):290-5.
2004: Onda Masamitsu; Nagai Hisaki; Yoshida Akira; Miyamoto Shizuyo; Asaka Shin-Ichi; Akaishi Junko; Takatsu Keisuke; Nagahama Mitsuji; Ito Kouichi; Shimizu Kazuo; Emi Mitsuru
Up-regulation of transcriptional factor E2F1 in papillary and anaplastic thyroid cancers.
Journal of human genetics 2004;49(6):312-8.
2004: Sato Keiko; Emi Mitsuru; Ezura Yoichi; Fujita Yuko; Takada Daisuke; Ishigami Tomoaki; Umemura Satoshi; Xin Yunpei; Wu Lily L; Larrinaga-Shum Stacey; Stephenson Susan H; Hunt Steven C; Hopkins Paul N
Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia: intrafamilial association study in an eight-generation hyperlipidemic kindred.
Journal of human genetics 2004;49(1):29-34.
2004: Fujita Yuko; Ezura Yoichi; Emi Mitsuru; Sato Keiko; Takada Daisuke; Iino Yasuhiko; Katayama Yasuo; Takahashi Kaneo; Kamimura Kouhei; Bujo Hideaki; Saito Yasushi
Hypercholesterolemia associated with splice-junction variation of inter-alpha-trypsin inhibitor heavy chain 4 (ITIH4) gene.
Journal of human genetics 2004;49(1):24-8.
2003: Ezura Yoichi; Nakajima Toshiaki; Kajita Mitsuko; Ishida Ryota; Inoue Satoshi; Yoshida Hideyo; Suzuki Takao; Shiraki Masataka; Hosoi Takayuki; Orimo Hajime; Emi Mitsuru
Association of molecular variants, haplotypes, and linkage disequilibrium within the human vitamin D-binding protein (DBP) gene with postmenopausal bone mineral density.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2003;18(9):1642-9.
2003: Okino Keiko; Nagai Hisaki; Hatta Mitsuko; Nagahata Takemitsu; Yoneyama Koichi; Ohta Yujiro; Jin Enjing; Kawanami Oichi; Araki Tsutomu; Emi Mitsuru
Up-regulation and overproduction of DVL-1, the human counterpart of the Drosophila dishevelled gene, in cervical squamous cell carcinoma.
Oncology reports 2003;10(5):1219-23.
2003: Ishida Ryota; Ezura Yoichi; Emi Mitsuru; Kajita Mitsuko; Yoshida Hideo; Suzuki Takao; Hosoi Takayuki; Inoue Satoshi; Shiraki Masataka; Ito Hiromoto; Orimo Hajime
Association of a promoter haplotype (-1542G/-525C) in the tumor necrosis factor receptor associated factor-interacting protein gene with low bone mineral density in Japanese women.
Bone 2003;33(2):237-41.
2003: Takada Daisuke; Ezura Yoichi; Ono Shuji; Iino Yasuhiko; Katayama Yasuo; Xin Yuanpei; Wu Lily L; Larringa-Shum Stacey; Stephenson Susan H; Hunt Steven C; Hopkins Paul N; Emi Mitsuru
Growth hormone receptor variant (L526I) modifies plasma HDL cholesterol phenotype in familial hypercholesterolemia: intra-familial association study in an eight-generation hyperlipidemic kindred.
American journal of medical genetics. Part A 2003;121A(2):136-40.
2003: Nagahata Takemitsu; Shimada Takashi; Harada Akima; Nagai Hisaki; Onda Masamitsu; Yokoyama Shiro; Shiba Tadayoshi; Jin Enjing; Kawanami Oichi; Emi Mitsuru
Amplification, up-regulation and over-expression of DVL-1, the human counterpart of the Drosophila disheveled gene, in primary breast cancers.
Cancer science 2003;94(6):515-8.
2003: Nagai H; Yabe A; Mine N; Mikami I; Fujiwara H; Terada Y; Hirano A; Tsuneizumi M; Yokota T; Emi M
Down-regulation in human cancers of DRHC, a novel helicase-like gene from 17q25.1 that inhibits cell growth.
Cancer letters 2003;193(1):41-7.
2003: Ishida Ryota; Emi Mitsuru; Ezura Yoichi; Iwasaki Hironori; Yoshida Hideyo; Suzuki Takao; Hosoi Takayuki; Inoue Satoshi; Shiraki Masataka; Ito Hiromoto; Orimo Hajime
Association of a haplotype (196Phe/532Ser) in the interleukin-1-receptor-associated kinase (IRAK1) gene with low radial bone mineral density in two independent populations.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2003;18(3):419-23.
2003: Iwasaki Hironori; Emi Mitsuru; Ezura Yoichi; Ishida Ryota; Kajita Mitsuko; Kodaira Mina; Yoshida Hideyo; Suzuki Takao; Hosoi Takayuki; Inoue Satoshi; Shiraki Masataka; Swensen Jeff; Orimo Hajime
Association of a Trp16Ser variation in the gonadotropin releasing hormone signal peptide with bone mineral density, revealed by SNP-dependent PCR typing.
Bone 2003;32(2):185-90.
2003: Fujimoto Takashi; Onda Masamitsu; Nagai Hisaki; Nagahata Takemitsu; Ogawa Kenji; Emi Mitsuru
Upregulation and overexpression of human X-box binding protein 1 (hXBP-1) gene in primary breast cancers.
Breast cancer (Tokyo, Japan) 2003;10(4):301-6.
2003: Yokota Takashi; Tachizawa Takayuki; Fukino Koichi; Teramoto Akira; Kouno Jun; Matsumoto Koshi; Emi Mitsuru
A family with spinal anaplastic ependymoma: evidence of loss of chromosome 22q in tumor.
Journal of human genetics 2003;48(11):598-602.
2003: Ono Shuji; Ezura Yoichi; Emi Mitsuru; Fujita Yuko; Takada Daisuke; Sato Keiko; Ishigami Tomoaki; Umemura Satoshi; Takahashi Kaneo; Kamimura Kouhei; Bujo Hideaki; Saito Yasushi
A promoter SNP (-1323T>C) in G-substrate gene (GSBS) correlates with hypercholesterolemia.
Journal of human genetics 2003;48(9):447-50.
2003: Omasu Fumihiro; Ezura Yoichi; Kajita Mitsuko; Ishida Ryota; Kodaira Mina; Yoshida Hideo; Suzuki Takao; Hosoi Takayuki; Inoue Satoshi; Shiraki Masataka; Orimo Hajime; Emi Mitsuru
Association of genetic variation of the RIL gene, encoding a PDZ-LIM domain protein and localized in 5q31.1, with low bone mineral density in adult Japanese women.
Journal of human genetics 2003;48(7):342-5.
2003: Fujita Yuko; Ezura Yoichi; Emi Mitsuru; Ono Shuji; Takada Daisuke; Takahashi Kaneo; Uemura Kouhei; Iino Yasuhiko; Katayama Yasuo; Bujo Hideaki; Saito Yasushi
Hypertriglyceridemia associated with amino acid variation Asn985Tyr of the RP1 gene.
Journal of human genetics 2003;48(6):305-8.
2003: Takada Daisuke; Ezura Yoichi; Ono Shuji; Iino Yasuhiko; Katayama Yasuo; Xin Yuanpei; Wu Lily L; Larringa-Shum Stacey; Stephenson Susan H; Hunt Steven C; Hopkins Paul N; Emi Mitsuru
Apolipoprotein H variant modifies plasma triglyceride phenotype in familial hypercholesterolemia: a molecular study in an eight-generation hyperlipidemic family.
Journal of atherosclerosis and thrombosis 2003;10(2):79-84.
2003: Kajita Mitsuko; Ezura Yoichi; Iwasaki Hironori; Ishida Ryota; Yoshida Hideyo; Kodaira Mina; Suzuki Takao; Hosoi Takayuki; Inoue Satoshi; Shiraki Masataka; Orimo Hajime; Emi Mitsuru
Association of the -381T/C promoter variation of the brain natriuretic peptide gene with low bone-mineral density and rapid postmenopausal bone loss.
Journal of human genetics 2003;48(2):77-81.
2002: Nagai Hisaki; Kim Yong Sung; Konishi Noboru; Baba Masaru; Kubota Takeo; Yoshimura Akihiko; Emi Mitsuru
Combined hypermethylation and chromosome loss associated with inactivation of SSI-1/SOCS-1/JAB gene in human hepatocellular carcinomas.
Cancer letters 2002;186(1):59-65.
2002: Shimizu Masashi; Kosaka Natsuki; Shimada Takashi; Nagahata Takemitsu; Iwasaki Hironori; Nagai Hisaki; Shiba Tadayoshi; Emi Mitsuru
Universal fluorescent labeling (UFL) method for automated microsatellite analysis.
DNA research : an international journal for rapid publication of reports on genes and genomes 2002;9(5):173-8.
2002: Shinohara Y; Ezura Y; Iwasaki H; Nakazawa I; Ishida R; Nakajima T; Kodaira M; Kajita M; Shiba T; Emi M
Three TNFalpha single nucleotide polymorphisms in the Japanese population.
Annals of human biology 2002;29(5):579-83.
2002: Ota N; Nakajima T; Ezura Y; Iwasaki H; Suzuki T; Hosoi T; Orimo H; Inoue S; Ito H; Emi M
Association of a single nucleotide variant in the human tumour necrosis factor alpha promoter region with decreased bone mineral density.
Annals of human biology 2002;29(5):550-8.
2002: Harada Haruhito; Nagai Hisaki; Ezura Yoichi; Yokota Takashi; Ohsawa Ikuroh; Yamaguchi Kenjiro; Ohue Chiharu; Tsuneizumi Michiko; Mikami Iwao; Terada Yoshie; Yabe Aya; Emi Mitsuru
Down-regulation of a novel gene, DRLM, in human liver malignancy from 4q22 that encodes a NAP-like protein.
Gene 2002;296(1-2):171-7.
2002: Tsuneizumi Michiko; Nagai Hisaki; Harada Haruhito; Kazui Teruhisa; Emi Mitsuu
A highly polymorphic CA repeat marker at the EBAG9/RCAS1 locus on 8q23 that detected frequent multiplication in breast cancer.
Annals of human biology 2002;29(4):457-60.
2002: Tsuneizumi Michiko; Emi Mitsuru; Hirano Akira; Utada Yoshihito; Tsumagari Koji; Takahashi Kaoru; Kasumi Fujio; Akiyama Futoshi; Sakamoto Goi; Kazui Teruhisa; Nakamura Yusuke
Association of allelic loss at 8p22 with poor prognosis among breast cancer cases treated with high-dose adjuvant chemotherapy.
Cancer letters 2002;180(1):75-82.
2002: Iwasaki Hironori; Ezura Yoichi; Ishida Ryota; Kajita Mitsuko; Kodaira Mina; Knight Jim; Daniel Steve; Shi Michael; Emi Mitsuru
Accuracy of genotyping for single nucleotide polymorphisms by a microarray-based single nucleotide polymorphism typing method involving hybridization of short allele-specific oligonucleotides.
DNA research : an international journal for rapid publication of reports on genes and genomes 2002;9(2):59-62.
2002: Harada Haruhito; Yoshida Shoko; Nobe Yukiko; Ezura Yoichi; Atake Tomoko; Koguchi Tomoko; Emi Mitsuru
Genomic structure of the human NLK (nemo-like kinase) gene and analysis of its promoter region.
Gene 2002;285(1-2):175-82.
2002: Nakajima Toshiaki; Jorde Lynn B; Ishigami Tomoaki; Umemura Satoshi; Emi Mitsuru; Lalouel Jean-Marc; Inoue Ituro
Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations.
American journal of human genetics 2002;70(1):108-23.
2002: Takada Daisuke; Emi Mitsuru; Ezura Yoichi; Nobe Yukiko; Kawamura Katsumi; Iino Yasuhiko; Katayama Yasuo; Xin Yuanpei; Wu Lily L; Larringa-Shum Stacey; Stephenson Susan H; Hunt Steven C; Hopkins Paul N
Interaction between the LDL-receptor gene bearing a novel mutation and a variant in the apolipoprotein A-II promoter: molecular study in a 1135-member familial hypercholesterolemia kindred.
Journal of human genetics 2002;47(12):656-64.
2002: Yoshida Shoko; Harada Haruhito; Nagai Hisaki; Fukino Kouichi; Teramoto Akira; Emi Mitsuru
Head-to-head juxtaposition of Fas-associated phosphatase-1 (FAP-1) and c-Jun NH2-terminal kinase 3 (JNK3) genes: genomic structure and seven polymorphisms of the FAP-1 gene.
Journal of human genetics 2002;47(11):614-9.
2002: Nagahata Takemitsu; Hirano Akira; Utada Yoshihito; Tsuchiya Shinichi; Takahashi Kaoru; Tada Takashi; Makita Masujirou; Kasumi Fujio; Akiyama Futoshi; Sakamoto Goi; Nakamura Yusuke; Emi Mitsuru
Correlation of allelic losses and clinicopathological factors in 504 primary breast cancers.
Breast cancer (Tokyo, Japan) 2002;9(3):208-15.
2002: Harada Haruhito; Kimura Akinori; Fukino Koichi; Yasunaga Seikoh; Nishi Hirofumi; Emi Mitsuru
Genomic structure and eight novel exonic polymorphisms of the human N-cadherin gene.
Journal of human genetics 2002;47(6):330-2.
2002: Ishii Jun; Nagano Makoto; Kujiraoka Takeshi; Ishihara Mitsuaki; Egashira Tohru; Takada Daisuke; Tsuji Masahiro; Hattori Hiroaki; Emi Mitsuru
Clinical variant of Tangier disease in Japan: mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis.
Journal of human genetics 2002;47(7):366-9.
2002: Hattori Hiroaki; Hirayama Tsunenori; Nobe Yukiko; Nagano Makoto; Kujiraoka Takeshi; Egashira Tohru; Ishii Jun; Tsuji Masahiro; Emi Mitsuru
Eight novel mutations and functional impairments of the LDL receptor in familial hypercholesterolemia in the north of Japan.
Journal of human genetics 2002;47(2):80-7.
2001: Haga S; Emi M; Hirano A; Utada Y; Kajiwara T; Akiyama F; Sakamoto G; Takahashi K; Tada T; Kasumi F; Miki Y; Nakamura Y
Association of allelic losses at 3p25.1, 13q12, or 17p13.3 with poor prognosis in breast cancers with lymph node metastasis.
Japanese journal of cancer research : Gann 2001;92(11):1199-206.
2001: Tsuneizumi M; Emi M; Nagai H; Harada H; Sakamoto G; Kasumi F; Inoue S; Kazui T; Nakamura Y
Overrepresentation of the EBAG9 gene at 8q23 associated with early-stage breast cancers.
Clinical cancer research : an official journal of the American Association for Cancer Research 2001;7(11):3526-32.
2001: Terada Y; Imoto I; Nagai H; Suwa K; Momoi M; Tajiri T; Onda M; Inazawa J; Emi M
An 8-cM interstitial deletion on 4q21-q22 in DNA from an infant with hepatoblastoma overlaps with a commonly deleted region in adult liver cancers.
American journal of medical genetics 2001;103(2):176-80.
2001: Kitamura Y; Shimizu K; Ito K; Tanaka S; Emi M
Allelotyping of follicular thyroid carcinoma: frequent allelic losses in chromosome arms 7q, 11p, and 22q.
The Journal of clinical endocrinology and metabolism 2001;86(9):4268-72.
2001: Hirano A; Nagai H; Harada H; Haga S; Kajiwara T; Emi M
Two novel single-nucleotide polymorphisms of the Caspase-9 (CASP9) gene in the Japanese population.
Genes and immunity 2001;2(2):117-8.
2001: Mikami I; Harada H; Nagai H; Tsuneizumi M; Nobe Y; Koizumi K; Sugano S; Tanaka S; Emi M
Down-regulation in multiple human cancers of a novel gene, DMHC, from 17q25.1 that encodes an integral membrane protein.
Japanese journal of cancer research : Gann 2001;92(4):417-22.
2001: Yokota T; Nagai H; Harada H; Mine N; Terada Y; Fujiwara H; Yabe A; Miyazaki K; Emi M
Identification, tissue expression, and chromosomal position of a novel gene encoding human ubiquitin-conjugating enzyme E2-230k.
Gene 2001;267(1):95-100.
2001: Hirano A; Emi M; Tsuneizumi M; Utada Y; Yoshimoto M; Kasumi F; Akiyama F; Sakamoto G; Haga S; Kajiwara T; Nakamura Y
Allelic losses of loci at 3p25.1, 8p22, 13q12, 17p13.3, and 22q13 correlate with postoperative recurrence in breast cancer.
Clinical cancer research : an official journal of the American Association for Cancer Research 2001;7(4):876-82.
2001: Nagai H; Kim Y S; Lee K T; Chu M Y; Konishi N; Fujimoto J; Baba M; Matsubara K; Emi M
Inactivation of SSI-1, a JAK/STAT inhibitor, in human hepatocellular carcinomas, as revealed by two-dimensional electrophoresis.
Journal of hepatology 2001;34(3):416-21.
2001: Hirano A; Utada Y; Haga S; Kajiwara T; Sakamoto G; Kasumi F; Nakamura Y; Emi M
Allelic losses as prognostic markers for breast cancers.
International journal of clinical oncology / Japan Society of Clinical Oncology 2001;6(1):6-12.
2001: Mine N; Kurose K; Konishi H; Araki T; Nagai H; Emi M
Fusion of a sequence from HEI10 (14q11) to the HMGIC gene at 12q15 in a uterine leiomyoma.
Japanese journal of cancer research : Gann 2001;92(2):135-9.
2001: Kurose K; Mine N; Iida A; Nagai H; Harada H; Araki T; Emi M
Three aberrant splicing variants of the HMGIC gene transcribed in uterine leiomyomas.
Genes, chromosomes & cancer 2001;30(2):212-7.
2001: Ishida R; Ezura Y; Iwasaki H; Nakazawa I; Kajita M; Kodaira M; Ito H; Emi M
Linkage disequilibrium and haplotype analysis among four novel single-nucleotide polymorphisms in the human leukemia inhibitory factor (LIF) gene.
Journal of human genetics 2001;46(10):557-9.
2001: Iwasaki H; Shinohara Y; Ezura Y; Ishida R; Kodaira M; Kajita M; Nakajima T; Shiba T; Emi M
Thirteen single-nucleotide polymorphisms in the human osteopontin gene identified by sequencing of the entire gene in Japanese individuals.
Journal of human genetics 2001;46(9):544-6.
2001: Shinohara Y; Ezura Y; Iwasaki H; Nakazawa I; Ishida R; Kodaira M; Kajita M; Shiba T; Emi M
Linkage disequilibrium and haplotype analysis among ten single-nucleotide polymorphisms of interleukin 11 identified by sequencing of the gene.
Journal of human genetics 2001;46(8):494-7.
2001: Mine N; Kurose K; Nagai H; Doi D; Ota Y; Yoneyama K; Konishi H; Araki T; Emi M
Gene fusion involving HMGIC is a frequent aberration in uterine leiomyomas.
Journal of human genetics 2001;46(7):408-12.
2001: Fujiwara H; Emi M; Nagai H; Ohgaki K; Imoto I; Akimoto M; Ogawa O; Habuchi T
Definition of a 1-Mb homozygous deletion at 9q32-q33 in a human bladder-cancer cell line.
Journal of human genetics 2001;46(7):372-7.
2001: Nakazawa I; Nakajima T; Ishigami T; Umemura S; Emi M
Linkage disequilibrium and haplotype analysis among eight novel single-nucleotide polymorphisms in the human tissue-type plasminogen activator (t-PA) gene.
Journal of human genetics 2001;46(7):367-71.
2001: Ota N; Nakajima T; Nakazawa I; Suzuki T; Hosoi T; Orimo H; Inoue S; Shirai Y; Emi M
A nucleotide variant in the promoter region of the interleukin-6 gene associated with decreased bone mineral density.
Journal of human genetics 2001;46(5):267-72.
2001: Yoshida S; Fukino K; Harada H; Nagai H; Imoto I; Inazawa J; Takahashi H; Teramoto A; Emi M
The c-Jun NH2-terminal kinase3 (JNK3) gene: genomic structure, chromosomal assignment, and loss of expression in brain tumors.
Journal of human genetics 2001;46(4):182-7.
2001: Nakazawa I; Nakajima T; Harada H; Ishigami T; Umemura S; Emi M
Human calcitonin receptor-like receptor for adrenomedullin: genomic structure, eight single-nucleotide polymorphisms, and haplotype analysis.
Journal of human genetics 2001;46(3):132-6.
2001: Shinohara Y; Iwasaki H; Ota N; Nakajima T; Kodaira M; Kajita M; Shiba T; Emi M
Novel single nucleotide polymorphisms of the human nuclear factor kappa-B 2 gene identified by sequencing the entire gene.
Journal of human genetics 2001;46(1):50-1.
2001: Kajita M; Iwasaki H; Ota N; Shinohara Y; Kodaira M; Nakajima T; Emi M
Novel single nucleotide polymorphisms of the human colony-stimulating factor 2 (CSF2) gene identified by sequencing the entire gene.
Journal of human genetics 2001;46(1):48-9.
2001: Hirano A; Nagai H; Harada H; Terada Y; Haga S; Kajiwara T; Emi M
Nine novel single-nucleotide polymorphisms in the integrin beta4 (ITGB4) gene in the Japanese population.
Journal of human genetics 2001;46(1):35-7.
2001: Iwasaki H; Ota N; Nakajima T; Shinohara Y; Kodaira M; Kajita M; Emi M
Five novel single-nucleotide polymorphisms of human interferon gamma identified by sequencing the entire gene.
Journal of human genetics 2001;46(1):32-4.
2001: Keicho N; Emi M; Kajita M; Matsushita I; Nakata K; Azuma A; Ohishi N; Kudoh S
Overestimated frequency of a possible emphysema-susceptibility allele when microsomal epoxide hydrolase is genotyped by the conventional polymerase chain reaction-based method.
Journal of human genetics 2001;46(2):96-8.
2001: Harada H; Nagai H; Tsuneizumi M; Mikami I; Sugano S; Emi M
Identification of DMC1, a novel gene in the TOC region on 17q25.1 that shows loss of expression in multiple human cancers.
Journal of human genetics 2001;46(2):90-5.
2001: Harada H; Nagai H; Mine N; Terada Y; Fujiwara H; Mikami I; Tsuneizumi M; Yabe A; Miyazaki K; Yokota T; Imoto I; Inazawa J; Emi M
Molecular cloning, tissue expression, and chromosomal assignment of a novel gene encoding a subunit of the human signal-recognition particle.
Journal of human genetics 2001;46(2):70-5.
2000: Utada Y; Emi M; Yoshimoto M; Kasumi F; Akiyama F; Sakamoto G; Haga S; Kajiwara T; Nakamura Y
Allelic loss at 1p34-36 predicts poor prognosis in node-negative breast cancer.
Clinical cancer research : an official journal of the American Association for Cancer Research 2000;6(8):3193-8.
2000: Nagai H; Emi M
[Palmoplantar keratosis]
Nippon rinsho. Japanese journal of clinical medicine 2000;58(7):1501-4.
2000: Koyama M; Nagai H; Bando K; Matsumoto S; Tajiri T; Onda M; Ito M; Moriyama Y; Emi M
New target region of allelic loss in hepatocellular carcinomas within a 1-cM interval on chromosome 6q23.
Journal of hepatology 2000;33(1):85-90.
2000: Mikami I; Nagai H; Harada H; Emi M
[Methods of single-nucleotide polymorphism analysis and application to hereditary cancer syndrome]
Nippon rinsho. Japanese journal of clinical medicine 2000;58(6):1220-4.
2000: Kitamura Y; Shimizu K; Tanaka S; Ito K; Emi M
Association of allelic loss on 1q, 4p, 7q, 9p, 9q, and 16q with postoperative death in papillary thyroid carcinoma.
Clinical cancer research : an official journal of the American Association for Cancer Research 2000;6(5):1819-25.
2000: Bando K; Nagai H; Matsumoto S; Koyama M; Kawamura N; Tajiri T; Onda M; Emi M
Identification of a 1-Mb common region at 16q24.1-24.2 deleted in hepatocellular carcinoma.
Genes, chromosomes & cancer 2000;28(1):38-44.
2000: Utada Y; Emi M; Haga S; Kajiwara T
[Allelic loss as prognostic factor in breast cancer]
Nippon rinsho. Japanese journal of clinical medicine 2000;58 Suppl():473-7.
2000: Nagai H; Harada H; Emi M
[Oncogene and tumor suppressor gene]
Nippon rinsho. Japanese journal of clinical medicine 2000;58 Suppl():25-9.
2000: Matsumoto S; Minobe K; Utada Y; Furukawa K; Onda M; Sakamoto G; Kasumi F; Nakamura Y; Emi M
Loss of heterozygosity at 3p24-p25 as a prognostic factor in breast cancer.
Cancer letters 2000;152(1):63-9.
2000: Iida A; Emi M; Matsuoka R; Hiratsuka E; Okui K; Ohashi H; Inazawa J; Fukushima Y; Imai T; Nakamura Y
Identification of a gene disrupted by inv(11)(q13.5;q25) in a patient with left-right axis malformation.
Human genetics 2000;106(3):277-87.
2000: Utada Y; Haga S; Kajiwara T; Kasumi F; Sakamoto G; Nakamura Y; Emi M
Mapping of target regions of allelic loss in primary breast cancers to 1-cM intervals on genomic contigs at 6q21 and 6q25.3.
Japanese journal of cancer research : Gann 2000;91(3):293-300.
2000: Utada Y; Haga S; Kajiwara T; Kasumi F; Sakamoto G; Nakamura Y; Emi M
Allelic loss at the 8p22 region as a prognostic factor in large and estrogen receptor negative breast carcinomas.
Cancer 2000;88(6):1410-6.
2000: Ogawa S; Hosoi T; Shiraki M; Orimo H; Emi M; Muramatsu M; Ouchi Y; Inoue S
Association of estrogen receptor beta gene polymorphism with bone mineral density.
Biochemical and biophysical research communications 2000;269(2):537-41.
2000: Kurose K; Mine N; Doi D; Ota Y; Yoneyama K; Konishi H; Araki T; Emi M
Novel gene fusion of COX6C at 8q22-23 to HMGIC at 12q15 in a uterine leiomyoma.
Genes, chromosomes & cancer 2000;27(3):303-7.
2000: Kitamura Y; Shimizu K; Tanaka S; Ito K; Emi M
Allelotyping of anaplastic thyroid carcinoma: frequent allelic losses on 1q, 9p, 11, 17, 19p, and 22q.
Genes, chromosomes & cancer 2000;27(3):244-51.
2000: Tsukamoto K; Orimo H; Hosoi T; Miyao M; Ota N; Nakajima T; Yoshida H; Watanabe S; Suzuki T; Emi M
Association of bone mineral density with polymorphism of the human calcium-sensing receptor locus.
Calcified tissue international 2000;66(3):181-3.
2000: Keicho N; Ohashi J; Tamiya G; Nakata K; Taguchi Y; Azuma A; Ohishi N; Emi M; Park M H; Inoko H; Tokunaga K; Kudoh S
Fine localization of a major disease-susceptibility locus for diffuse panbronchiolitis.
American journal of human genetics 2000;66(2):501-7.
2000: Kohro T; Nakajima T; Wada Y; Sugiyama A; Ishii M; Tsutsumi S; Aburatani H; Imoto I; Inazawa J; Hamakubo T; Kodama T; Emi M
Genomic structure and mapping of human orphan receptor LXR alpha: upregulation of LXRa mRNA during monocyte to macrophage differentiation.
Journal of atherosclerosis and thrombosis 2000;7(3):145-51.
2000: Ota N; Hunt S C; Nakajima T; Suzuki T; Hosoi T; Orimo H; Shirai Y; Emi M
Linkage of human tumor necrosis factor-alpha to human osteoporosis by sib pair analysis.
Genes and immunity 2000;1(4):260-4.
2000: Miyao M; Hosoi T; Emi M; Nakajima T; Inoue S; Hoshino S; Shiraki M; Orimo H; Ouchi Y
Association of bone mineral density with a dinucleotide repeat polymorphism at the calcitonin (CT) locus.
Journal of human genetics 2000;45(6):346-50.
2000: Ogawa S; Emi M; Shiraki M; Hosoi T; Ouchi Y; Inoue S
Association of estrogen receptor beta (ESR2) gene polymorphism with blood pressure.
Journal of human genetics 2000;45(6):327-30.
2000: Nakajima T; Iwaki K; Hamakubo T; Kodama T; Emi M
Genomic structure of the gene encoding human 3-hydroxy-3-methyl-glutaryl coenzyme A reductase: comparison of exon/intron organization of sterol-sensing domains among four related genes.
Journal of human genetics 2000;45(5):284-9.
2000: Orimo H; Nakajima E; Yamamoto M; Ikejima M; Emi M; Shimada T
Association between single nucleotide polymorphisms in the hMSH3 gene and sporadic colon cancer with microsatellite instability.
Journal of human genetics 2000;45(4):228-30.
2000: Nakajima T; Iwaki K; Kodama T; Inazawa J; Emi M
Genomic structure and chromosomal mapping of the human site-1 protease (S1P) gene.
Journal of human genetics 2000;45(4):212-7.
2000: Wu L L; Hopkins P N; Xin Y; Stephenson S H; Williams R R; Nobe Y; Kajita M; Nakajima T; Emi M
Co-segregation of elevated LDL with a novel mutation (D92K) of the LDL receptor in a kindred with multiple lipoprotein abnormalities.
Journal of human genetics 2000;45(3):154-8.
2000: Fukino K; Teramoto A; Adachi K; Takahashi H; Emi M
A family with hydrocephalus as a complication of cerebellar hemangioblastoma: identification of Pro157Leu mutation in the VHL gene.
Journal of human genetics 2000;45(1):47-51.
2000: Yokota T; Nakata T; Minami S; Inazawa J; Emi M
Genomic organization and chromosomal mapping of ELKS, a gene rearranged in a papillary thyroid carcinoma.
Journal of human genetics 2000;45(1):6-11.
2000: Tsukamoto K; Orimo H; Hosoi T; Miyao M; Yoshida H; Watanabe S; Suzuki T; Emi M
Association of bone mineral density with polymorphism of the human matrix Gla protein locus in elderly women.
Journal of bone and mineral metabolism 2000;18(1):27-30.
1999: Orimo H; Nakajima E; Ikejima M; Emi M; Shimada T
Frameshift mutations and a length polymorphism in the hMSH3 gene and the spectrum of microsatellite instability in sporadic colon cancer.
Japanese journal of cancer research : Gann 1999;90(12):1310-5.
1999: Ota N; Nakajima T; Takeuchi T; Shirai Y; Emi M
A highly polymorphic CA repeat marker at the interleukin-11 locus.
Genes and immunity 1999;1(2):159-60.
1999: Nakajima T; Ota N; Yoshida H; Watanabe S; Suzuki T; Emi M
Allelic variants in the interleukin-6 gene and essential hypertension in Japanese women.
Genes and immunity 1999;1(2):115-9.
1999: Nakajima T; Ota N; Shirai Y; Hata A; Yoshida H; Suzuki T; Hosoi T; Orimo H; Emi M
Ethnic difference in contribution of Sp1 site variation of COLIA1 gene in genetic predisposition to osteoporosis.
Calcified tissue international 1999;65(5):352-3.
1999: Keicho N; Emi M; Nakata K; Taguchi Y; Azuma A; Tokunaga K; Ohishi N; Kudoh S
Promoter variation of tumour necrosis factor-alpha gene: possible high risk for chronic bronchitis but not diffuse panbronchiolitis.
Respiratory medicine 1999;93(10):752-3.
1999: Nagai H; Emi M
[Genome and cDNA analysis of human hepatocellular carcinoma]
Nippon Ika Daigaku zasshi 1999;66(5):324-6.
1999: Kitamura Y; Shimizu K; Tanaka S; Emi M
[Genetic alterations in thyroid carcinomas]
Nippon Ika Daigaku zasshi 1999;66(5):319-23.
1999: Nakajima T; Emi M
[Molecular variants of the human angiotensinogen gene associated with essential hypertension]
Nippon Ika Daigaku zasshi 1999;66(5):313-5.
1999: Emi M; Yoshimoto M; Sato T; Matsumoto S; Utada Y; Ito I; Minobe K; Iwase T; Katagiri T; Bando K; Akiyama F; Harada Y; Fukino K; Sakamoto G; Matsushima M; Iida A; Tada T; Saito H; Miki Y; Kasumi F; Nakamura Y
Allelic loss at 1p34, 13q12, 17p13.3, and 17q21.1 correlates with poor postoperative prognosis in breast cancer.
Genes, chromosomes & cancer 1999;26(2):134-41.
1999: Ota N; Hunt S C; Nakajima T; Suzuki T; Hosoi T; Orimo H; Shirai Y; Emi M
Linkage of interleukin 6 locus to human osteopenia by sibling pair analysis.
Human genetics 1999;105(3):253-7.
1999: Ohgaki K; Minobe K; Kurose K; Iida A; Habuchi T; Ogawa O; Kubota Y; Akimoto M; Emi M
Two target regions of allelic loss on chromosome 9 in urinary-bladder cancer.
Japanese journal of cancer research : Gann 1999;90(9):957-64.
1999: Koyama M; Nagai H; Bando K; Ito M; Moriyama Y; Emi M
Localization of a target region of allelic loss to a 1-cM interval on chromosome 16p.13.13 in hepatocellular carcinoma.
Japanese journal of cancer research : Gann 1999;90(9):951-6.
1999: Fukino K; Kitamura Y; Sanno N; Teramoto A; Emi M
Analysis of the MEN1 gene in sporadic pituitary adenomas from Japanese patients.
Cancer letters 1999;144(1):85-92.
1999: Minobe K; Bando K; Fukino K; Soma S; Kasumi F; Sakamoto G; Furukawa K; Higuchi K; Onda M; Nakamura Y; Emi M
Somatic mutation of the PTEN/MMAC1 gene in breast cancers with microsatellite instability.
Cancer letters 1999;144(1):9-16.
1999: Katsumata H; Emi M; Nobe Y; Nakajima T; Hirayama T; Wu L L; Stephenson S H; Hopkins P N; Williams R R
Familial hypercholesterolemia in Utah kindred with novel R103W mutations in exon 4 of the LDL receptor gene.
Japanese heart journal 1999;40(4):443-9.
1999: Nobe Y; Emi M; Katsumata H; Nakajima T; Hirayama T; Wu L L; Stephenson S H; Hopkins P N; Williams R R
Familial hypercholesterolemia in Utah kindred with novel 2412-6 Ins G mutations in exon 17 of the LDL receptor gene.
Japanese heart journal 1999;40(4):435-41.
1999: Tsukamoto K; Yoshimoto M; Kasumi F; Akiyama F; Sakamoto G; Nakamura Y; Emi M
Frequent multiplication of chromosome 1q in non-invasive and papillotubular carcinoma of the breast.
Cancer letters 1999;141(1-2):21-8.
1999: Bando K; Nagai H; Matsumoto S; Koyama M; Kawamura N; Onda M; Emi M
Identification of a 1-cM region of common deletion on 4q35 associated with progression of hepatocellular carcinoma.
Genes, chromosomes & cancer 1999;25(3):284-9.
1999: Nakata T; Kitamura Y; Shimizu K; Tanaka S; Fujimori M; Yokoyama S; Ito K; Emi M
Fusion of a novel gene, ELKS, to RET due to translocation t(10;12)(q11;p13) in a papillary thyroid carcinoma.
Genes, chromosomes & cancer 1999;25(2):97-103.
1999: Yokota T; Yoshimoto M; Akiyama F; Sakamoto G; Kasumi F; Nakamura Y; Emi M
Frequent multiplication of chromosomal region 8q24.1 associated with aggressive histologic types of breast cancers.
Cancer letters 1999;139(1):7-13.
1999: Ohgaki K; Iida A; Ogawa O; Kubota Y; Akimoto M; Emi M
Localization of tumor suppressor gene associated with distant metastasis of urinary bladder cancer to a 1-Mb interval on 8p22.
Genes, chromosomes & cancer 1999;25(1):1-5.
1999: Kawamura N; Nagai H; Bando K; Koyama M; Matsumoto S; Tajiri T; Onda M; Fujimoto J; Ueki T; Konishi N; Shiba T; Emi M
PTEN/MMAC1 mutations in hepatocellular carcinomas: somatic inactivation of both alleles in tumors.
Japanese journal of cancer research : Gann 1999;90(4):413-8.
1999: Keicho N; Tokunaga K; Nakata K; Taguchi Y; Azuma A; Tanabe K; Matsushita M; Emi M; Ohishi N; Kudoh S
Contribution of TAP genes to genetic predisposition for diffuse panbronchiolitis.
Tissue antigens 1999;53(4 Pt 1):366-73.
1999: Fukino K; Iido A; Teramoto A; Sakamoto G; Kasumi F; Nakamura Y; Emi M
Frequent allelic loss at the TOC locus on 17q25.1 in primary breast cancers.
Genes, chromosomes & cancer 1999;24(4):345-50.
1999: Yokota T; Yoshimoto M; Akiyama F; Sakamoto G; Kasumi F; Nakamura Y; Emi M
Localization of a tumor suppressor gene associated with the progression of human breast carcinoma within a 1-cM interval of 8p22-p23.1.
Cancer 1999;85(2):447-52.
1999: Iwaki K; Nakajima T; Ota N; Emi M
A common Ile796Val polymorphism of the human SREBP cleavage-activating protein (SCAP) gene.
Journal of human genetics 1999;44(6):421-2.
1999: Nakajima T; Hamakubo T; Kodama T; Inazawa J; Emi M
Genomic structure and chromosomal mapping of the human sterol regulatory element binding protein (SREBP) cleavage-activating protein (SCAP) gene.
Journal of human genetics 1999;44(6):402-7.
1999: Hopkins P N; Wu L L; Stephenson S H; Xin Y; Katsumata H; Nobe Y; Nakajima T; Hirayama T; Emi M; Williams R R
A novel LDLR mutation, H190Y, in a Utah kindred with familial hypercholesterolemia.
Journal of human genetics 1999;44(6):364-7.
1999: Mine N; Bando K; Utada Y; Nagai H; Araki T; Emi M
Two single nucleotide polymorphisms of the hSNF5/INI1 gene.
Journal of human genetics 1999;44(5):354-5.
1999: Nakajima T; Ota N; Kodama T; Emi M
Isolation and radiation hybrid mapping of a highly polymorphic CA repeat sequence at the SREBP cleavage-activating protein (SCAP) locus.
Journal of human genetics 1999;44(5):350-1.
1999: Emi M; Keicho N; Tokunaga K; Katsumata H; Souma S; Nakata K; Taguchi Y; Ohishi N; Azuma A; Kudoh S
Association of diffuse panbronchiolitis with microsatellite polymorphism of the human interleukin 8 (IL-8) gene.
Journal of human genetics 1999;44(3):169-72.
1999: Tsukamoto K; Yoshida H; Watanabe S; Suzuki T; Miyao M; Hosoi T; Orimo H; Emi M
Association of radial bone mineral density with CA repeat polymorphism at the interleukin 6 locus in postmenopausal Japanese women.
Journal of human genetics 1999;44(3):148-51.
1999: Ota N; Nakajima T; Shirai Y; Emi M
Isolation and radiation hybrid mapping of a highly polymorphic CA repeat sequence at the human nuclear factor kappa-beta subunit 1 (NFKB1) locus.
Journal of human genetics 1999;44(2):129-30.
1999: Kitamura Y; Minobe K; Nakata T; Shimizu K; Tanaka S; Fujimori M; Yokoyama S; Ito K; Onda M; Emi M
Ret/PTC3 is the most frequent form of gene rearrangement in papillary thyroid carcinomas in Japan.
Journal of human genetics 1999;44(2):96-102.
1998: Emi M; Yamaki E; Hirayama T; Katsumata H; Pozharov V; Wu L L; Hopkins P N; Williams R R
Familial hypercholesterolemia kindred in Utah with novel C54S mutations of the LDL receptor gene.
Japanese heart journal 1998;39(6):785-9.
1998: Ohgaki K; Iida A; Kasumi F; Sakamoto G; Akimoto M; Nakamura Y; Emi M
Mapping of a new target region of allelic loss to a 6-cM interval at 21q21 in primary breast cancers.
Genes, chromosomes & cancer 1998;23(3):244-7.
1998: Yamaki E; Hirayama T; Wu L L; Hopkins P N; Williams R R; Emi M
Molecular genetic diagnosis of a family with hypercholesterolemia by a mismatched PCR-RFLP method for genotyping single base substitution of the LDL receptor gene.
Japanese heart journal 1998;39(5):681-6.
1998: Minobe K; Onda M; Iida A; Kasumi F; Sakamoto G; Nakamura Y; Emi M
Allelic loss on chromosome 9q is associated with lymph node metastasis of primary breast cancer.
Japanese journal of cancer research : Gann 1998;89(9):916-22.
1998: Keicho N; Tokunaga K; Nakata K; Taguchi Y; Azuma A; Bannai M; Emi M; Ohishi N; Yazaki Y; Kudoh S
Contribution of HLA genes to genetic predisposition in diffuse panbronchiolitis.
American journal of respiratory and critical care medicine 1998;158(3):846-50.
1998: Kurose K; Bando K; Fukino K; Sugisaki Y; Araki T; Emi M
Somatic mutations of the PTEN/MMAC1 gene in fifteen Japanese endometrial cancers: evidence for inactivation of both alleles.
Japanese journal of cancer research : Gann 1998;89(8):842-8.
1998: Orimo H; Ikejima M; Nakajima E; Emi M; Shimada T
A novel missense mutation and frameshift mutations in the type II receptor of transforming growth factor-beta gene in sporadic colon cancer with microsatellite instability.
Mutation research 1998;382(3-4):115-20.
1998: Kurose K; Iida A; Araki T; Sakamoto G; Kasumi F; Nakamura Y; Emi M
Frequent allelic loss at 7p14-15 associated with aggressive histologic types of breast cancer.
Japanese journal of cancer research : Gann 1998;89(5):533-8.
1998: Iida A; Kurose K; Isobe R; Akiyama F; Sakamoto G; Yoshimoto M; Kasumi F; Nakamura Y; Emi M
Mapping of a new target region of allelic loss to a 2-cM interval at 22q13.1 in primary breast cancer.
Genes, chromosomes & cancer 1998;21(2):108-12.
1998: Emi M; Matsushima M; Katagiri T; Yoshimoto M; Kasumi F; Yokota T; Nakata T; Miki Y; Nakamura Y
Multiplex mutation screening of the BRCA1 gene in 1000 Japanese breast cancers.
Japanese journal of cancer research : Gann 1998;89(1):12-6.
1998: Tsukamoto K; Ito N; Yoshimoto M; Kasumi F; Akiyama F; Sakamoto G; Nakamura Y; Emi M
Allelic loss on chromosome 1p is associated with progression and lymph node metastasis of primary breast carcinoma.
Cancer 1998;82(2):317-22.
1998: Tsukamoto K; Ohta N; Shirai Y; Emi M
A highly polymorphic CA repeat marker at the human interleukin 6 receptor (IL6R) locus.
Journal of human genetics 1998;43(4):289-90.
1998: Tsukamoto K; Watanabe I; Shiba T; Emi M
Isolation of a polymorphic CA repeat sequence at the human progesterone receptor (PGR) locus.
Journal of human genetics 1998;43(4):287-8.
1998: Tsukamoto K; Watanabe I; Shiba T; Emi M
Isolation and radiation hybrid mapping of a dinucleotide repeat polymorphism at the human calcium-sensing receptor (CASR) locus.
Journal of human genetics 1998;43(4):280-2.
1998: Tsukamoto K; Ohta N; Shirai Y; Emi M
A highly polymorphic CA repeat marker at the human tumor necrosis factor alpha (TNFA alpha) locus.
Journal of human genetics 1998;43(4):278-9.
1998: Hirayama T; Yamaki E; Hata A; Tsuji M; Hashimoto K; Yamamoto M; Emi M
Five familial hypercholesterolemic kindreds in Japan with novel mutations of the LDL receptor gene.
Journal of human genetics 1998;43(4):250-4.
1998: Tsukamoto K; Emi M
A polymorphic CA repeat sequence at the human calcitonin locus.
Journal of human genetics 1998;43(2):146-7.
1998: Watanabe I; Tsukamoto K; Shiba T; Emi M
Isolation and radiation hybrid mapping of dinucleotide repeat polymorphism at the human matrix Gla protein (MGP) locus.
Journal of human genetics 1998;43(1):75-6.
1998: Tsukamoto K; Inoue S; Hosoi T; Orimo H; Emi M
Isolation and radiation hybrid mapping of dinucleotide repeat polymorphism at the human estrogen receptor beta locus.
Journal of human genetics 1998;43(1):73-4.
1998: Tsukamoto K; Haruta K; Shiba T; Emi M
Isolation and mapping of a polymorphic CA repeat sequence at the human interleukin 6 locus.
Journal of human genetics 1998;43(1):71-2.
1997: Matsumoto S; Kasumi F; Sakamoto G; Onda M; Nakamura Y; Emi M
Detailed deletion mapping of chromosome arm 3p in breast cancers: a 2-cM region on 3p14.3-21.1 and a 5-cM region on 3p24.3-25.1 commonly deleted in tumors.
Genes, chromosomes & cancer 1997;20(3):268-74.
1997: Yokota T; Matsumoto S; Yoshimoto M; Kasumi F; Akiyama F; Sakamoto G; Nakamura Y; Emi M
Mapping of a breast cancer tumor suppressor gene locus to a 4-cM interval on chromosome 18q21.
Japanese journal of cancer research : Gann 1997;88(10):959-64.
1997: Iida A; Matsumoto S; Emi M
[Breast cancers]
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme 1997;42(10 Suppl):1754-61.
1997: Iida A; Isobe R; Yoshimoto M; Kasumi F; Nakamura Y; Emi M
Localization of a breast cancer tumour-suppressor gene to a 3-cM interval within chromosomal region 16q22.
British journal of cancer 1997;75(2):264-7.
1996: Tsukamoto K; Emi M; Nakamura Y
[Cytogenetic abnormalities, genetic alterations, and applications for genetic diagnosis in breast cancer]
Nippon rinsho. Japanese journal of clinical medicine 1996;54(12):3389-97.
1996: Tsukamoto K; Ito N; Yoshimoto M; Iwase T; Tada T; Kasumi F; Nakamura Y; Emi M
Two distinct commonly deleted regions on chromosome 13q suggest involvement of BRCA2 and retinoblastoma genes in sporadic breast carcinomas.
Cancer 1996;78(9):1929-34.
1996: Matsumoto S; Emi M; Kasumi F; Nakamura Y
[Genetic alterations and DNA-based diagnosis in breast cancer]
Nippon Geka Gakkai zasshi 1996;97(5):375-80.
1996: Emi M; Iida A; Kasumi F; Nakamura Y
[Genetic alterations in familial and sporadic breast cancers]
Gan to kagaku ryoho. Cancer & chemotherapy 1996;23 Suppl 1():80-3.
1995: Emi M
[DNA-based diagnosis of breast cancer cases]
Nippon Ika Daigaku zasshi 1995;62(5):512-5.
1993: Hata A; Ridinger D N; Sutherland S; Emi M; Shuhua Z; Myers R L; Ren K; Cheng T; Inoue I; Wilson D E
Binding of lipoprotein lipase to heparin. Identification of five critical residues in two distinct segments of the amino-terminal domain.
The Journal of biological chemistry 1993;268(12):8447-57.
1992: Hata A; Ridinger D N; Sutherland S D; Emi M; Kwong L K; Shuhua J; Lubbers A; Guy-Grand B; Basdevant A; Iverius P H
Missense mutations in exon 5 of the human lipoprotein lipase gene. Inactivation correlates with loss of dimerization.
The Journal of biological chemistry 1992;267(28):20132-9.
1991: Hopkins P N; Wu L L; Schumacher M C; Emi M; Hegele R M; Hunt S C; Lalouel J M; Williams R R
Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interaction.
Arteriosclerosis and thrombosis : a journal of vascular biology / American Heart Association 1991;11(5):1137-46.
1991: Emi M; Hegele R M; Hopkins P N; Wu L L; Plaetke R; Williams R R; Lalouel J M
Effects of three genetic loci in a pedigree with multiple lipoprotein phenotypes.
Arteriosclerosis and thrombosis : a journal of vascular biology / American Heart Association 1991;11(5):1349-55.
1991: Hegele R A; Sutherland S; Robertson M; Wu L; Emi M; Hopkins P N; Williams R R; Lalouel J M
The effect of genetic determinants of low density lipoprotein levels on lipoprotein (a).
Clinical and investigative medicine. Médecine clinique et experimentale 1991;14(2):146-52.
1990: Hata A; Emi M; Luc G; Basdevant A; Gambert P; Iverius P H; Lalouel J M
Compound heterozygote for lipoprotein lipase deficiency: Ser----Thr244 and transition in 3' splice site of intron 2 (AG----AA) in the lipoprotein lipase gene.
American journal of human genetics 1990;47(4):721-6.
1990: Wilson D E; Emi M; Iverius P H; Hata A; Wu L L; Hillas E; Williams R R; Lalouel J M
Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation.
The Journal of clinical investigation 1990;86(3):735-50.
1990: Hata A; Robertson M; Emi M; Lalouel J M
Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene.
Nucleic acids research 1990;18(18):5407-11.
1990: Emi M; Hata A; Robertson M; Iverius P H; Hegele R; Lalouel J M
Lipoprotein lipase deficiency resulting from a nonsense mutation in exon 3 of the lipoprotein lipase gene.
American journal of human genetics 1990;47(1):107-11.
1990: Marshall B C; Sageser D S; Rao N V; Emi M; Hoidal J R
Alveolar epithelial cell plasminogen activator. Characterization and regulation.
The Journal of biological chemistry 1990;265(14):8198-204.
1990: Emi M; Wilson D E; Iverius P H; Wu L; Hata A; Hegele R; Williams R R; Lalouel J M
Missense mutation (Gly----Glu188) of human lipoprotein lipase imparting functional deficiency.
The Journal of biological chemistry 1990;265(10):5910-6.
1989: Hegele R A; Nakamura Y; Emi M; Lalouel J M; White R
Two RFLPs at the lipoprotein lipase (LPL) gene.
Nucleic acids research 1989;17(23):10146.
1989: Hegele R A; Nakamura Y; Emi M; Lalouel J M; White R
A BglII RFLP at the lipoprotein lipase gene.
Nucleic acids research 1989;17(21):8899.
1989: Hegele R A; Emi M; Nakamura Y; Lalouel J M; White R
A StuI RFLP upstream of the low density lipoprotein receptor (LDLR) gene.
Nucleic acids research 1989;17(4):1786.
1989: Hegele R A; Emi M; Wu L L; Hopkins P N; Williams R R; Lalouel J M
Clinical application of deoxyribonucleic acid markers in a Utah family with hypercholesterolemia.
The American journal of cardiology 1989;63(1):109-12.
1989: Hegele R A; Emi M; Nakamura Y; Lalouel J M; White R
Three RFLPs upstream of the low density lipoprotein receptor (LDLR) gene.
Nucleic acids research 1989;17(1):470.
1988: Hegele R A; Emi M; Nakamura Y; Lalouel J M; White R
RFLPs upstream of the low-density lipoprotein receptor (LDLR) gene.
Nucleic acids research 1988;16(14B):7214.

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