Kangni Zheng

发表

Somatic mitochondrial DNA mutations in single neurons and glia

M. Beal, D. Standaert, R. Betensky, 2005, Neurobiology of Aging.

A Common NURR 1 Polymorphism Associated With Parkinson Disease and Diffuse Lewy Body Disease

D. Simon, Bobak Heydari, Kangni Zheng, 2003 .

Pgc-1α Overexpression Downregulates Pitx3 and Increases Susceptibility to MPTP Toxicity Associated with Decreased Bdnf

Jessica M. Silvaggi, C. Bass, D. Simon, 2012, PloS one.

Somatic mitochondrial DNA mutations do not increase neuronal vulnerability to MPTP in young POLG mutator mice.

T. Prolla, D. Simon, G. Kujoth, 2014, Neurotoxicology and teratology.

Determination of colistin in animal tissues, egg, milk, and feed by ultra-high performance liquid chromatography-tandem mass spectrometry.

X. Xia, Xiaowei Li, Yuebin Ke, 2018, Food chemistry.

Mitochondrial complex I gene variant associated with early age at onset in spinocerebellar ataxia type 2.

S. Pulst, D. Simon, K. Figueroa, 2007, Archives of neurology.

Purkinje neuron degeneration in nervous (nr) mutant mice is mediated by a metabolic pathway involving excess tissue plasminogen activator

R. Sidman, E. Snyder, Jianxue Li, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Suppression of Reactive Oxygen Species and Neurodegeneration by the PGC-1 Transcriptional Coactivators

Jiandie D. Lin, Jessica M. Silvaggi, B. Spiegelman, 2006, Cell.

Behavioral and metabolic characterization of heterozygous and homozygous POLG mutator mice.

T. Prolla, D. Simon, E. Maratos-Flier, 2013, Mitochondrion.

Association of PGC-1alpha polymorphisms with age of onset and risk of Parkinson's disease

R. Betensky, D. Simon, Kangni Zheng, 2011, BMC Medical Genetics.

Zfp281 (ZBP-99) plays a functionally redundant role with Zfp148 (ZBP-89) during erythroid development.

E. Fraenkel, Jianlong Wang, A. Cantor, 2019, Blood advances.

A common NURR1 polymorphism associated with Parkinson disease and diffuse Lewy body disease.

D. Simon, Bobak Heydari, Kangni Zheng, 2003, Archives of neurology.

Oral N-Acetyl-Cysteine Attenuates Loss of Dopaminergic Terminals in α-Synuclein Overexpressing Mice

E. Masliah, D. Simon, A. Adame, 2010, PloS one.

Rapamycin drives selection against a pathogenic heteroplasmic mitochondrial DNA mutation.

S. Pulst, R. Swerdlow, D. Simon, 2014, Human molecular genetics.

Somatic mitochondrial DNA mutations in early parkinson and incidental lewy body disease

M. Beal, A. Lees, T. Arzberger, 2012, Annals of neurology.