[PDF][PDF] A potent and specific CD38 inhibitor ameliorates age-related metabolic dysfunction by reversing tissue NAD+ decline

…, A Caride, GC de Oliveira, M Rud, A Samani… - Cell metabolism, 2018 - cell.com
Aging is characterized by the development of metabolic dysfunction and frailty. Recent studies
show that a reduction in nicotinamide adenine dinucleotide (NAD + ) is a key factor for the …

Tumor-derived cytokines impair myogenesis and alter the skeletal muscle immune microenvironment

KA Hogan, DS Cho, PC Arneson, A Samani, P Palines… - Cytokine, 2018 - Elsevier
Muscle wasting is a decline in skeletal muscle mass and function that is associated with aging,
obesity, and a spectrum of pathologies including cancer. Cancer-associated wasting not …

miR-486 is essential for muscle function and suppresses a dystrophic transcriptome

A Samani, RM Hightower, AL Reid… - Life Science …, 2022 - life-science-alliance.org
miR-486 is a muscle-enriched microRNA, or “myomiR,” that has reduced expression
correlated with Duchenne muscular dystrophy (DMD). To determine the function of miR-486 in …

DOCK3 is a dosage-sensitive regulator of skeletal muscle and Duchenne muscular dystrophy-associated pathologies

AL Reid, Y Wang, A Samani… - Human Molecular …, 2020 - academic.oup.com
DOCK3 is a member of the DOCK family of guanine nucleotide exchange factors that
regulate cell migration, fusion and viability. Previously, we identified a dysregulated miR-486/…

The wasting‐associated metabolite succinate disrupts myogenesis and impairs skeletal muscle regeneration

…, KA Hogan, AM Ducharme, A Samani… - JCSM rapid …, 2020 - Wiley Online Library
Background Muscle wasting is a debilitating co‐morbidity affecting most advanced cancer
patients. Alongside enhanced muscle catabolism, defects in muscle repair/regeneration …

[HTML][HTML] Next-Generation SINE Compound KPT− 8602 Ameliorates Dystrophic Pathology in Zebrafish and Mouse Models of DMD

KG English, AL Reid, A Samani, GJF Coulis, SA Villalta… - Biomedicines, 2022 - mdpi.com
Duchenne muscular dystrophy (DMD) is a progressive, X-linked childhood neuromuscular
disorder that results from loss-of-function mutations in the DYSTROPHIN gene. DMD patients …

DOCKopathies: A systematic review of the clinical pathologies associated with human DOCK pathogenic variants

A Samani, KG English, MA Lopez, CL Birch… - Human …, 2022 - Wiley Online Library
The Dedicator of Cytokinesis (DOCK) family (DOCK1−11) of genes are essential mediators
of cellular migration, growth, and fusion in a variety of cell types and tissues. Recent …

[HTML][HTML] DOCK3 regulates normal skeletal muscle regeneration and glucose metabolism

A Samani, M Karuppasamy, KG English, CA Siler… - bioRxiv, 2023 - ncbi.nlm.nih.gov
DOCK (dedicator of cytokinesis) is an 11-member family of typical guanine nucleotide exchange
factors (GEFs) expressed in the brain, spinal cord, and skeletal muscle. Several DOCK …

miR-486 is an epigenetic modulator of Duchenne muscular dystrophy pathologies

RM Hightower, A Samani, AL Reid, KG English… - BioRxiv, 2021 - biorxiv.org
Duchenne muscular dystrophy (DMD) is an X-linked progressive muscle disorder resulting
in muscle weakness and cardiomyopathy. MicroRNAs have been shown to play essential …

DOCK3 IS ESSENTIAL FOR NORMAL MUSCLE REGENERATION AND GLUCOSE METABOLISM

A SAMANI, Y WANG, KG ENGLISH… - The Role of DOCK3 In … - search.proquest.com
DOCK (dedicator of cytokinesis) proteins are an 11-member family of typical guanine
exchange factors (GEFs) expressed in the brain and spinal cord. Several DOCK proteins have …