Preliminary observations of mitochondrial dysfunction in Prader-Willi syndrome

SustainedO-GlcNAcylation reprograms mitochondrial function to regulate energy metabolism

(2017) Ee Phie Tan et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Arsenite Effects on Mitochondrial Bioenergetics in Human and Mouse Primary Hepatocytes Follow a Nonlinear Dose Response

(2017) Hemantkumar Chavan et al.   Oxidative Medicine and Cellular Longevity

L-Arginine improves DNA synthesis in LPS-challenged enterocytes

(2015) Bi'e Tan   Frontiers in Bioscience-Landmark

Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings

(2015) M. A. Angulo et al.   JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION

Differential Gene Expression Reveals Mitochondrial Dysfunction in an Imprinting Center Deletion Mouse Model of Prader-Willi Syndrome

(2013) Puya G. Yazdi et al.   CTS-Clinical and Translational Science

The Electrophile Responsive Proteome: Integrating Proteomics and Lipidomics with Cellular Function

(2012) Ashlee N. Higdon et al.   ANTIOXIDANTS & REDOX SIGNALING

Prader-Willi Syndrome: Obesity due to Genomic Imprinting

(2012) Merlin G. Butler   CURRENT GENOMICS

Prader-Willi syndrome

(2012) Suzanne B. Cassidy et al.   GENETICS IN MEDICINE

Assessing mitochondrial dysfunction in cells

(2011) Martin D. Brand et al.   BIOCHEMICAL JOURNAL

Nitric oxide and hypoxia exacerbate alcohol-induced mitochondrial dysfunction in hepatocytes

(2011) Blake R. Zelickson et al.   BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS

Assessing bioenergetic function in response to oxidative stress by metabolic profiling

(2011) Brian P. Dranka et al.   FREE RADICAL BIOLOGY AND MEDICINE

The Regulation and Physiology of Mitochondrial Proton Leak

(2011) Ajit S. Divakaruni et al.   PHYSIOLOGY

Developmental profiles in young children with Prader–Labhart–Willi syndrome: Effects of weight and therapy with growth hormone or coenzyme Q10

(2008) Urs Eiholzer et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Depletion of mitochondrial DNA in fibroblast cultures from patients with POLG1 mutations is a consequence of catalytic mutations

(2008) Neil Ashley et al.   HUMAN MOLECULAR GENETICS