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Jia-huan Ding

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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TOP 3
Chen Shuyuan; Ding Jia-huan; Bekeredjian Raffi; Yang Bing-zhi; Shohet Ralph V; Johnston Stephen A; Hohmeier Hans E; Newgard Christopher B; Grayburn Paul A
Efficient gene delivery to pancreatic islets with ultrasonic microbubble destruction technology.
Zhang Li-Feng; Ding Jia-Huan; Yang Bing-Zhi; He Guo-Cheng; Roe Charles
Characterization of the bidirectional promoter region between the human genes encoding VLCAD and PSD-95.
Yang B Z; Mallory J M; Roe D S; Brivet M; Strobel G D; Jones K M; Ding J H; Roe C R
Carnitine/acylcarnitine translocase deficiency (neonatal phenotype): successful prenatal and postmortem diagnosis associated with a novel mutation in a single family.

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2006: Chen Shuyuan; Ding Jia-huan; Bekeredjian Raffi; Yang Bing-zhi; Shohet Ralph V; Johnston Stephen A; Hohmeier Hans E; Newgard Christopher B; Grayburn Paul A
Efficient gene delivery to pancreatic islets with ultrasonic microbubble destruction technology.
Proceedings of the National Academy of Sciences of the United States of America 2006;103(22):8469-74.
2003: Zhang Li-Feng; Ding Jia-Huan; Yang Bing-Zhi; He Guo-Cheng; Roe Charles
Characterization of the bidirectional promoter region between the human genes encoding VLCAD and PSD-95.
Genomics 2003;82(6):660-8.
2001: Yang B Z; Mallory J M; Roe D S; Brivet M; Strobel G D; Jones K M; Ding J H; Roe C R
Carnitine/acylcarnitine translocase deficiency (neonatal phenotype): successful prenatal and postmortem diagnosis associated with a novel mutation in a single family.
Molecular genetics and metabolism 2001;73(1):64-70.
2000: Yang B Z; Ding J H; Zhou C; Dimachkie M M; Sweetman L; Dasouki M J; Wilkinson J; Roe C R
Identification of a novel mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency.
Molecular genetics and metabolism 2000;69(3):259-62.
1999: He G; Yang B Z; Roe D S; Teramoto R; Aleck K; Grebe T A; Roe C R; Ding J H
Identification of two novel mutations in the hypoglycemic phenotype of very long chain acyl-CoA dehydrogenase deficiency.
Biochemical and biophysical research communications 1999;264(2):483-7.
1998: Yang B Z; Ding J H; Dewese T; Roe D; He G; Wilkinson J; Day D W; Demaugre F; Rabier D; Brivet M; Roe C
Identification of four novel mutations in patients with carnitine palmitoyltransferase II (CPT II) deficiency.
Molecular genetics and metabolism 1998;64(4):229-36.
1998: Yang B Z; Ding J H; Roe D; Dewese T; Day D W; Roe C R
A novel mutation identified in carnitine palmitoyltransferase II deficiency.
Molecular genetics and metabolism 1998;63(2):110-5.
1996: Yang B Z; Heng H H; Ding J H; Roe C R
The genes for the alpha and beta subunits of the mitochondrial trifunctional protein are both located in the same region of human chromosome 2p23.
Genomics 1996;37(1):141-3.
1996: Ding J H; Yang B Z; Nada M A; Roe C R
Improved detection of the G1528C mutation in LCHAD deficiency.
Biochemical and molecular medicine 1996;58(1):46-51.
1996: Nada M A; Vianey-Saban C; Roe C R; Ding J H; Mathieu M; Wappner R S; Bialer M G; McGlynn J A; Mandon G
Prenatal diagnosis of mitochondrial fatty acid oxidation defects.
Prenatal diagnosis 1996;16(2):117-24.
1994: Andresen B S; Jensen T G; Bross P; Knudsen I; Winter V; Kølvraa S; Bolund L; Ding J H; Chen Y T; Van Hove J L
Disease-causing mutations in exon 11 of the medium-chain acyl-CoA dehydrogenase gene.
American journal of human genetics 1994;54(6):975-88.
1993: Van Hove J L; Zhang W; Kahler S G; Roe C R; Chen Y T; Terada N; Chace D H; Iafolla A K; Ding J H; Millington D S
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood.
American journal of human genetics 1993;52(5):958-66.
1992: Yang B Z; Ding J H; Enghild J J; Bao Y; Chen Y T
Molecular cloning and nucleotide sequence of cDNA encoding human muscle glycogen debranching enzyme.
The Journal of biological chemistry 1992;267(13):9294-9.
1992: Ding J H; Yang B Z; Bao Y; Roe C R; Chen Y T
Identification of a new mutation in medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.
American journal of human genetics 1992;50(1):229-33.
1992: Ding J H; Bross P; Yang B Z; Iafolla A K; Millington D S; Roe C R; Gregersen N; Chen Y T
Genetic heterogeneity in MCAD deficiency: frequency of K329E allele and identification of three additional mutant alleles.
Progress in clinical and biological research 1992;375():479-88.
1992: Millington D S; Terada N; Chace D H; Chen Y T; Ding J H; Kodo N; Roe C R
The role of tandem mass spectrometry in the diagnosis of fatty acid oxidation disorders.
Progress in clinical and biological research 1992;375():339-54.
1991: Ding J H; Roe C R; Iafolla A K; Chen Y T
Medium-chain acyl-coenzyme A dehydrogenase deficiency and sudden infant death.
The New England journal of medicine 1991;325(1):61-2.
1991: Yang B Z; Stewart C; Ding J H; Chen Y T
Type III glycogen storage disease: an adult case with mild disease but complete absence of debrancher protein.
Neuromuscular disorders : NMD 1991;1(3):173-6.
1990: Yang B Z; Ding J H; Brown B I; Chen Y T
Definitive prenatal diagnosis for type III glycogen storage disease.
American journal of human genetics 1990;47(4):735-9.
1990: Ding J H; de Barsy T; Brown B I; Coleman R A; Chen Y T
Immunoblot analyses of glycogen debranching enzyme in different subtypes of glycogen storage disease type III.
The Journal of pediatrics 1990;116(1):95-100.
1989: McConkie-Rosell A; Chen Y T; Harris D; Speer M C; Pericak-Vance M A; Ding J H; Highsmith W E; Knowles M; Kahler S G
Mild cystic fibrosis linked to chromosome 7q22 markers with an uncommon haplotype.
Annals of internal medicine 1989;111(10):797-801.
1987: Chen Y T; He J K; Ding J H; Brown B I
Glycogen debranching enzyme: purification, antibody characterization, and immunoblot analyses of type III glycogen storage disease.
American journal of human genetics 1987;41(6):1002-15.

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