Results 221 to 230 of about 1,104,554 (244)
Some of the next articles are maybe not open access.

Dystrophin-negative slow-twitch soleus muscles are not susceptible to eccentric contraction induced injury over the lifespan of the mdx mouse.

American Journal of Physiology - Cell Physiology, 2021
Duchenne muscular dystrophy (DMD) is the second most common fatal genetic disease in humans and is characterized by the absence of a functional copy of the protein dystrophin from skeletal muscle.
L. Kiriaev   +6 more
semanticscholar   +1 more source

Mss51 deletion increases endurance and ameliorates histopathology in the mdx mouse model of Duchenne muscular dystrophy

The FASEB Journal, 2021
Mitochondrial derangement is an important contributor to the pathophysiology of muscular dystrophies and may be among the earliest cellular deficits. We have previously shown that disruption of Mss51, a mammalian skeletal muscle protein that localizes to
Yazmin I Rovira Gonzalez   +12 more
semanticscholar   +1 more source

Expanded encyclopaedias of DNA elements in the human and mouse genomes

Nature, 2020
Jessika Adrian   +2 more
exaly  

The role of the microbiome in cancer development and therapy

Ca-A Cancer Journal for Clinicians, 2017
Aadra P Bhatt, Matthew R Redinbo
exaly  

Molecular subtypes of small cell lung cancer: a synthesis of human and mouse model data

Nature Reviews Cancer, 2019
Charles M Rudin   +2 more
exaly  

Topology of the human and mouse m6A RNA methylomes revealed by m6A-seq

Nature, 2012
Dan Dominissini   +2 more
exaly  

Genome-wide atlas of gene expression in the adult mouse brain

Nature, 2006
Ed S Lein   +2 more
exaly  

A single-cell transcriptomic atlas characterizes ageing tissues in the mouse

Nature, 2020
Biter Bilen   +2 more
exaly  

Initial sequencing and comparative analysis of the mouse genome

Nature, 2002
Kerstin Lindblad-Toh   +2 more
exaly  

Home - About - Disclaimer - Privacy