C. Pang

发表

Molecular epidemiologic study of mitochondrial DNA mutations in patients with mitochondrial diseases in Taiwan.

Y. Wei, C. C. Huang, E. K. Wang, 1999, Journal of the Formosan Medical Association = Taiwan yi zhi.

Human skin mitochondrial DNA deletions associated with light exposure.

H. C. Lee, Y. Wei, C. Pang, 1994, Archives of biochemistry and biophysics.

Age-dependent 6kb deletion in human liver mitochondrial DNA.

R. Hsieh, Y. Wei, K. L. King, 1992, Biochemistry international.

Increases of Mitochondrial Mass and Mitochondrial Genome in Association with Enhanced Oxidative Stress in Human Cells Harboring 4,977 BP‐Deleted Mitochondrial DNA

Yau-Huei Wei, Hsin-Chen Lee, C. Pang, 2001, Annals of the New York Academy of Sciences.

1-29-16 Large-scale mitochondrial DNA deletions in patients with CPEO syndrome in Taiwan

Yau-Huei Wei, R. Hsieh, E. K. Wang, 1997, Journal of the Neurological Sciences.

Myoclonic epilepsy with ragged‐red fibers (MERRF) syndrome: Report of a Chinese family with mitochondrial DNA point mutation in tRNALys gene

N. Chu, Rou-shayn Chen, Yau-Huei Wei, 1994, Muscle & nerve.

Vision improvement in a Taiwanese (Han Chinese) family with Leber's hereditary optic neuropathy

Shee-Ping Chen, R. Tsai, C. Pang, 2012, The Kaohsiung journal of medical sciences.

Enhanced oxidative damage in human cells harboring A3243G mutation of mitochondrial DNA: implication of oxidative stress in the pathogenesis of mitochondrial diabetes.

H. C. Lee, Y. Wei, C. Pang, 2001, Diabetes research and clinical practice.

Mitochondrial encephalomyopathies: CT and MRI findings and correlations with clinical features.

N. Chu, C. Liou, Y. Wai, 1995, European neurology.

Ophthalmologic manifestations in MELAS syndrome.

Y. Wei, C. Lee, C. Pang, 1993, Archives of neurology.

ROLES OF MITOCHONDRIAL DNA MUTATION AND OXIDATIVE DAMAGE IN HUMAN AGING

C. Pang, Y. Wei, H. Lee, 1998 .

Differential accumulations of 4,977 bp deletion in mitochondrial DNA of various tissues in human ageing.

H. C. Lee, Yau-Huei Wei, Hsin-Chen Lee, 1994, Biochimica et biophysica acta.

Oxidative Damage and Mutation to Mitochondrial DNA and Age‐dependent Decline of Mitochondrial Respiratory Function a

Yau-Huei Wei, Hsin-Chen Lee, YAU‐HUEI WEI, 1998, Annals of the New York Academy of Sciences.

Decreased cellular respiratory function and mitochondrial DNA mutations in the human heart associated with ageing and disease

Yau-Huei Wei, Hsin-Chen Lee, E. K. Wang, 1997 .

Tissue distribution of mutant mitochondrial DNA in a patient with MERRF syndrome

N. Chu, Rou-shayn Chen, Yau-Huei Wei, 1996, Muscle & nerve.

Peripheral neuropathy in mitochondrial encephalomyopathies.

N. Chu, Y. Wei, C. Chu, 1997, European neurology.

CPEO and carnitine deficiency overlapping in MELAS syndrome

J. Tsai, C. Pang, Y. Wei, 1995, Acta neurologica Scandinavica.

Mitochondrial DNA mutation in a Chinese family with myoclonic epilepsy and ragged-red fiber disease.

Yau-Huei Wei, Y. Wei, C. Pang, 1991, Biochemical and biophysical research communications.

Bioenergetic consequences of accumulating the common 4977-bp mitochondrial DNA deletion.

P. Sheard, M. Murphy, Yau-Huei Wei, 1998, European journal of biochemistry.

MtDNA mutations, functional decline and turnover of mitochondria in aging.

C. Pang, Yi‐Shing Ma, Yau-Uei Wei, 2008, Frontiers in bioscience : a journal and virtual library.

PDFlib PLOP: PDF Linearization, Optimization, Protection Page inserted by evaluation version

C. Pang, BAN‐JAU You, Hsin-Chen Lee, 2006 .

PDFlib PLOP: PDF Linearization, Optimization, Protection Page inserted by evaluation version

Yau-Huei Wei, Hsin-Chen Lee, C. Pang, 2002 .

Altered mitochondrial function in fibroblasts containing MELAS or MERRF mitochondrial DNA mutations.

M. Murphy, Yau-Huei Wei, Y. Wei, 1996, The Biochemical journal.

Mitochondrial DNA mutation in Leber's hereditary optic neuropathy.

Y. Wei, M. Yen, J. H. Liu, 1992, Investigative ophthalmology & visual science.

Mitochondrial myopathy with predominant respiratory dysfunction in a patient with A3243G mutation in the mitochondrial tRNA(Leu(UUR))gene.

Y. Wei, C. Pang, C. Hwang, 1998, Journal of the Formosan Medical Association = Taiwan yi zhi.

Overlapping syndrome of MERRF and MELAS: molecular and neuroradiological studies

Y. Wai, C. Pang, Y. Wei, 1993, Acta neurologica Scandinavica.

A Novel Mutation in the Mitochondrial 16S rRNA Gene in a Patient with MELAS Syndrome, Diabetes Mellitus, Hyperthyroidism and Cardiomyopathy

Yau-Huei Wei, R. Hsieh, C. Pang, 2001, Journal of Biomedical Science.

Leber's Hereditary Optic Neuropathy Associated with the m.10197G>A Mutation

R. Tsai, Tzu-Lun Huang, C. Pang, 2017 .

MELAS syndrome associated with a tandem duplication in the D‐loop of mitochondrial DNA

C. Pang, Y. Wei, H. Lee, 1996, Acta neurologica Scandinavica.

MELAS syndrome: correlation between clinical features and molecular genetic analysis

Y. Jong, C. Liou, J. Tsai, 1994, Acta neurologica Scandinavica.

Leigh syndrome associated with mitochondrial DNA 8993 T-->G mutation and ragged-red fibers.

Yau-Huei Wei, C. Chi, Ching-Shiang Chi, 1996, Pediatric neurology.

Random mitotic segregation of mitochondrial DNA in MELAS syndrome

N. Chu, C. Pang, Y. Wei, 1996, Acta neurologica Scandinavica.

MELAS syndrome with mitochondrial tRNA(Leu(UUR)) gene mutation in a Chinese family.

H. C. Lee, Rou-shayn Chen, Yau-Huei Wei, 1994, Journal of neurology, neurosurgery, and psychiatry.

Mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes (MELAS): report of a sporadic case and review of the literature.

Y. Jong, A. Yang, J. Tsai, 1994, Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui.

Tandem Duplications and Large‐Scale Deletions of Mitochondrial DNA Are Early Molecular Events of Human Aging Process a

Yau-Huei Wei, Hsin-Chen Lee, C. Pang, 1996, Annals of the New York Academy of Sciences.

Ageing‐associated tandem duplications in the D‐loop of mitochondrial DNA of human muscle

Hsin-Chen Lee, H. Hsu, C. Pang, 1994, FEBS letters.

High Prevalence of the COII/tRNALys Intergenic 9‐bp Deletion in Mitochondrial DNA of Taiwanese Patients with MELAS or MERRF Syndrome

Yau-Huei Wei, Yi-Yun Chen, W. Cheng, 2005, Annals of the New York Academy of Sciences.

Type IV hyperlipoproteinemia and moderate instability of CAG triplet expansion in the androgen‐receptor gene

C. Liu, C. Pang, Y. Wei, 1995, Acta neurologica Scandinavica.

Coenzyme Q10 treatment in Leber's hereditary optic neuropathy

Hung-Chou Kuo, Yau-Huei Wei, Hsin-Chen Lee, 2001 .

Independent occurrence of somatic mutations in mitochondrial DNA of human skin from subjects of various ages

Yau-Huei Wei, P. Nagley, Hsin-Chen Lee, 1998, Human mutation.