Jia-Huan Ding

Baylor University, Waco, TX 
Molecular Biology
"Jia-Huan Ding"
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Zhao Y, Feng Y, Zhang YM, et al. (2015) Targeted next-generation sequencing of candidate genes reveals novel mutations in patients with dilated cardiomyopathy. International Journal of Molecular Medicine
Zhao Y, Feng Y, Zhang YM, et al. (2015) Targeted Next-Generation Sequencing Reveals Hot Spots and Doubly Heterozygous Mutations in Chinese Patients with Familial Cardiomyopathy. Biomed Research International. 2015: 561819
Zhang LF, Ding JH, Yang BZ, et al. (2003) Characterization of the bidirectional promoter region between the human genes encoding VLCAD and PSD-95. Genomics. 82: 660-8
Yang BZ, Mallory JM, Roe DS, et al. (2001) Carnitine/acylcarnitine translocase deficiency (neonatal phenotype): successful prenatal and postmortem diagnosis associated with a novel mutation in a single family. Molecular Genetics and Metabolism. 73: 64-70
Yang B, Ding J, Zhou C, et al. (2000) Identification of a novel mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency. Molecular Genetics and Metabolism. 69: 259-262
He G, Yang B, Roe DS, et al. (1999) Identification Of Two Novel Mutations In The Hypoglycemic Phenotype Of Very Long Chain Acyl-Coa Dehydrogenase Deficiency Biochemical and Biophysical Research Communications. 264: 483-487
Yang B, Ding J, Dewese T, et al. (1998) Identification of Four Novel Mutations in Patients with Carnitine Palmitoyltransferase II (CPT II) Deficiency Molecular Genetics and Metabolism. 64: 229-236
Yang B, Ding J, Roe D, et al. (1998) A Novel Mutation Identified in Carnitine Palmitoyltransferase II Deficiency Molecular Genetics and Metabolism. 63: 110-115
Yang B, Heng HHQ, Ding J, et al. (1996) The Genes for the α and β Subunits of the Mitochondrial Trifunctional Protein Are Both Located in the Same Region of Human Chromosome 2p23 Genomics. 37: 141-143
Ding J, Yang B, Nada MA, et al. (1996) Improved Detection of the G1528C Mutation in LCHAD Deficiency Biochemical and Molecular Medicine. 58: 46-51
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