Physician
Medical Genetics
Dr. Taosheng Huang, MD
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Taosheng Huang is an expert in the field of Medical Genetics. He went to medical school at Fujian Medical University. Taosheng Huang is a published doctor as well. He has 9 publications published. The latest was: Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules.
Publications
- Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules.
- Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy.
- Mutations of Human NARS2, Encoding the Mitochondrial Asparaginyl-tRNA Synthetase, Cause Nonsyndromic Deafness and Leigh Syndrome.
- A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential.
- A splice donor mutation in NAA10 results in the dysregulation of the retinoic acid signalling pathway and causes Lenz microphthalmia syndrome.
- Heteroplasmic mutations of the mitochondrial genome cause paradoxical effects on mitochondrial functions.
- TBX3 Promotes Human Embryonic Stem Cell Proliferation and Neuroepithelial Differentiation in A Differentiation Stage-Dependent Manner.
- Species identification through mitochondrial rRNA genetic analysis.
Schools
Fujian Medical University
Georgetown University Hospital
Chldrn39s Hospital Harvard Med School
Doctors Specialties
- Clinical Genetics
- Clinical Molecular Genetics
- Pediatrics
- Medical Genetics
Accepted Insurances
Education
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Boston Children's Hospital -
Georgetown University Hospital -
Fujian Medical University
Hospital
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Children's Hospital of Orange County -
UC Irvine Medical Center
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