Myostatin inhibition promotes fast fibre hypertrophy but causes loss of AMP‐activated protein kinase signalling and poor exercise tolerance in a model of limb‐girdle …
I Kramerova, M Marinov, J Owens… - The Journal of …, 2020 - Wiley Online Library
Key points Limb‐girdle muscular dystrophy R1 (LGMD R1) is caused by mutations in the
CAPN3 gene and is characterized by progressive muscle loss, impaired mitochondrial …
CAPN3 gene and is characterized by progressive muscle loss, impaired mitochondrial …
Myostatin inhibition promotes fast fibre hypertrophy but causes loss of AMP-activated protein kinase signalling and poor exercise tolerance in a model of limb-girdle …
I Kramerova, M Marinov, J Owens… - The Journal of …, 2020 - pubmed.ncbi.nlm.nih.gov
Key points Limb-girdle muscular dystrophy R1 (LGMD R1) is caused by mutations in the
CAPN3 gene and is characterized by progressive muscle loss, impaired mitochondrial …
CAPN3 gene and is characterized by progressive muscle loss, impaired mitochondrial …
Myostatin inhibition promotes fast fibre hypertrophy but causes loss of AMP-activated protein kinase signalling and poor exercise tolerance in a model of limb-girdle …
I Kramerova, M Marinov, J Owens, SJ Lee… - The Journal of …, 2020 - europepmc.org
Limb-girdle muscular dystrophy R1 (LGMD R1) is caused by mutations in the CAPN3 gene
and is characterized by progressive muscle loss, impaired mitochondrial function and …
and is characterized by progressive muscle loss, impaired mitochondrial function and …
Myostatin inhibition promotes fast fibre hypertrophy but causes loss of AMP-activated protein kinase signalling and poor exercise tolerance in a model of limb-girdle …
I Kramerova, M Marinov, J Owens, SJ Lee… - Journal of …, 2020 - jhu.pure.elsevier.com
Key points: Limb-girdle muscular dystrophy R1 (LGMD R1) is caused by mutations in the
CAPN3 gene and is characterized by progressive muscle loss, impaired mitochondrial …
CAPN3 gene and is characterized by progressive muscle loss, impaired mitochondrial …
Myostatin inhibition promotes fast fibre hypertrophy but causes loss of AMP-activated protein kinase signalling and poor exercise tolerance in a model of limb-girdle …
I Kramerova, M Marinov, J Owens, SJ Lee… - Journal of …, 2020 - pure.johnshopkins.edu
Key points: Limb-girdle muscular dystrophy R1 (LGMD R1) is caused by mutations in the
CAPN3 gene and is characterized by progressive muscle loss, impaired mitochondrial …
CAPN3 gene and is characterized by progressive muscle loss, impaired mitochondrial …