DHPR α1S subunit controls skeletal muscle mass and morphogenesis

Introduction to the Review Series Autophagy in Higher Eukaryotes– A matter of survival or death

(2014) Ameeta Kelekar   Autophagy

Coordinate activation of autophagy and the proteasome pathway by FoxO transcription factor

(2014) Jinghui Zhao et al.   Autophagy

A Role for the CHC22 Clathrin Heavy-Chain Isoform in Human Glucose Metabolism

(2009) S. Vassilopoulos et al.   SCIENCE

Suppression of autophagy in skeletal muscle uncovers the accumulation of ubiquitinated proteins and their potential role in muscle damage in Pompe disease

(2008) N. Raben et al.   HUMAN MOLECULAR GENETICS

Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores

(2008) Nicole Monnier et al.   HUMAN MUTATION

A dihydropyridine receptor α1s loop region critical for skeletal muscle contraction is intrinsically unstructured and binds to a SPRY domain of the type 1 ryanodine receptor

(2008) Yanfang Cui et al.   INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY

CaMKII locally encodes L-type channel activity to signal to nuclear CREB in excitation–transcription coupling

(2008) Damian G. Wheeler et al.   JOURNAL OF CELL BIOLOGY

The Skeletal L-type Ca2+Current Is a Major Contributor to Excitation-coupled Ca2+entry

(2008) Roger A. Bannister et al.   JOURNAL OF GENERAL PHYSIOLOGY

Mechano-sensitivity of normal and long term denervated soleus muscle of the rat

(2008) Roberta Squecco et al.   NEUROLOGICAL RESEARCH

Lysosomal myopathies: An excessive build-up in autophagosomes is too much to handle

(2008) May Christine Malicdan et al.   NEUROMUSCULAR DISORDERS