Min Peng

发表

N-acetylcysteine and vitamin E rescue animal longevity and cellular oxidative stress in pre-clinical models of mitochondrial complex I disease.

Marni J. Falk, Zhe Zhang, C. Seiler, 2018, Molecular genetics and metabolism.

Parkinson's disease-like neuromuscular defects occur in prenyl diphosphate synthase subunit 2 (Pdss2) mutant mice.

Marni J. Falk, C. Ziegler, M. Falk, 2012, Mitochondrion.

The mitochondrial and kidney disease phenotypes of kd/kd mice under germfree conditions.

M. Madaio, D. Gasser, W. Hancock, 2006, Journal of autoimmunity.

Mutant prenyltransferase-like mitochondrial protein (PLMP) and mitochondrial abnormalities in kd/kd mice.

A. George, M. Madaio, E. Neilson, 2004, Kidney international.

Primary Coenzyme Q Deficiency in Pdss2 Mutant Mice Causes Isolated Renal Disease

Marni J. Falk, M. Yudkoff, M. Selak, 2008, PLoS genetics.

A novel STAT1 loss-of-function mutation associated with Mendelian susceptibility to mycobacterial disease

Fanghua Ye, Liang-chun Yang, Jiajia Dong, 2022, Frontiers in Cellular and Infection Microbiology.

Regulation and Evasion of Host Immune Response by African Swine Fever Virus

Ji-Long Chen, Xu Yuan, Min Peng, 2021, Frontiers in Microbiology.

Localization of the mouse kidney disease (kd) gene to a YAC/BAC contig on Chromosome 10

K. MacRae Dell, E. Neilson, D. Gasser, 2000, Mammalian Genome.

Primary Respiratory Chain Disease Causes Tissue-Specific Dysregulation of the Global Transcriptome and Nutrient-Sensing Signaling Network

Marni J. Falk, Zhe Zhang, E. Rappaport, 2013, PloS one.

Mitochondrial function requires NGLY1.

M. Falk, M. He, Y. Argon, 2018, Mitochondrion.

Novel TP53RK variants cause varied clinical features of Galloway–Mowat syndrome without nephrotic syndrome in three unrelated Chinese patients

J. Chen, Wei-yue Gu, Min Peng, 2023, Frontiers in Molecular Neuroscience.

Inhibiting cytosolic translation and autophagy improves health in mitochondrial disease.

Marni J. Falk, Zhe Zhang, C. Felix, 2015, Human molecular genetics.

Focal segmental glomerulosclerosis is associated with a PDSS2 haplotype and, independently, with a decreased content of coenzyme Q10.

C. Winkler, P. An, L. Mckenzie, 2013, American journal of physiology. Renal physiology.

Pre-clinical evaluation of cysteamine bitartrate as a therapeutic agent for mitochondrial respiratory chain disease.

Marni J. Falk, C. Seiler, M. Falk, 2019, Human molecular genetics.

Probucol ameliorates renal and metabolic sequelae of primary CoQ deficiency in Pdss2 mutant mice

Marni J. Falk, M. Falk, Zhe Zhang, 2011, EMBO molecular medicine.

Focal segmental glomerulosclerosis is associated with a PDSS 2 haplotype and , independently , with a decreased content of coenzyme Q 10

C. Winkler, P. An, L. Mckenzie, 2013 .

Glomerular and Tubular Epithelial Defects in kd/kd Mice Lead to Progressive Renal Failure

D. Rader, R. Ahima, M. Madaio, 2005, American Journal of Nephrology.