Muscle Pathology & Wasting Archives

Cellular rescue in a zebrafish model of congenital muscular dystrophy type 1A

Glucocorticoids Induce Bone and Muscle Atrophy by Tissue-Specific Mechanisms Upstream of E3 Ubiquitin Ligases

Contractile efficiency of dystrophic mdx mouse muscle: in vivo and ex vivo assessment of adaptation to exercise of functional end points

Oxidative stress-induced dysregulation of excitation–contraction coupling contributes to muscle weakness

Skeletal muscle function during the progression of cancer cachexia in the male ApcMin/+ mouse

Titin-based mechanosensing modulates muscle hypertrophy

Treating Spinal-Muscle Conditions

aursc20dev2021-09-27T15:18:37-04:00Muscle Physiology, Publication Review|

Featured image courtesy of Bilchak et al. (2021). Spinal disruption can lead to serious

Tips and Tricks for using the 1400A Permeabilized Fiber System

smcfr2021-11-09T14:34:30-05:00Muscle Physiology, Technical Blog|

Our 1400A permeabilized fiber system is commonly used to investigate the active and passive properties of skinned, or de-membranized

Slow-twitch skeletal muscle defects accompany cardiac dysfunction in transgenic mice with a mutation in the myosin regulatory light chain.

Slow-twitch skeletal muscle defects accompany cardiac dysfunction in transgenic mice with a mutation in the myosin regulatory light chain.

Xin-deficient mice display myopathy, impaired contractility, attenuated muscle repair and altered satellite cell functionality.

Masticatory muscles of mouse do not undergo atrophy in space.

Human trachealis and main bronchi smooth muscle are normoresponsive in asthma.

Human trachealis and main bronchi smooth muscle are normoresponsive in asthma.

Pompe disease results in a Golgi-based glycosylation deficit in human induced pluripotent stem cell-derived cardiomyocytes.

Characterization of a compartment syndrome-like injury model.

Alterations at the Cross-Bridge Level Are Associated with a Paradoxical Gain of Muscle Function In Vivo in a Mouse Model of Nemaline Myopathy

Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions.

Alterations at the Cross-Bridge Level Are Associated with a Paradoxical Gain of Muscle Function In Vivo in a Mouse Model of Nemaline Myopathy.

Long-term effects of Combat Ready Clamp application to control junctional hemorrhage in swine.

Functional, morphological, and apoptotic alterations in skeletal muscle of ARC deficient mice.

Single muscle contractile measurements in vivo and in situ.

Alterations at the Cross-Bridge Level Are Associated with a Paradoxical Gain of Muscle Function In Vivo in a Mouse Model of Nemaline Myopathy.

Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions.

Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions.

Cellular rescue in a zebrafish model of congenital muscular dystrophy type 1A

Glucocorticoids Induce Bone and Muscle Atrophy by Tissue-Specific Mechanisms Upstream of E3 Ubiquitin Ligases

Contractile efficiency of dystrophic mdx mouse muscle: in vivo and ex vivo assessment of adaptation to exercise of functional end points

Oxidative stress-induced dysregulation of excitation–contraction coupling contributes to muscle weakness

Skeletal muscle function during the progression of cancer cachexia in the male ApcMin/+ mouse

Titin-based mechanosensing modulates muscle hypertrophy

Treating Spinal-Muscle Conditions

Tips and Tricks for using the 1400A Permeabilized Fiber System

Slow-twitch skeletal muscle defects accompany cardiac dysfunction in transgenic mice with a mutation in the myosin regulatory light chain.

Slow-twitch skeletal muscle defects accompany cardiac dysfunction in transgenic mice with a mutation in the myosin regulatory light chain.

Xin-deficient mice display myopathy, impaired contractility, attenuated muscle repair and altered satellite cell functionality.

Masticatory muscles of mouse do not undergo atrophy in space.

Human trachealis and main bronchi smooth muscle are normoresponsive in asthma.

Human trachealis and main bronchi smooth muscle are normoresponsive in asthma.

Pompe disease results in a Golgi-based glycosylation deficit in human induced pluripotent stem cell-derived cardiomyocytes.

Characterization of a compartment syndrome-like injury model.

Alterations at the Cross-Bridge Level Are Associated with a Paradoxical Gain of Muscle Function In Vivo in a Mouse Model of Nemaline Myopathy

Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions.

Alterations at the Cross-Bridge Level Are Associated with a Paradoxical Gain of Muscle Function In Vivo in a Mouse Model of Nemaline Myopathy.

Long-term effects of Combat Ready Clamp application to control junctional hemorrhage in swine.

Functional, morphological, and apoptotic alterations in skeletal muscle of ARC deficient mice.

Single muscle contractile measurements in vivo and in situ.

Alterations at the Cross-Bridge Level Are Associated with a Paradoxical Gain of Muscle Function In Vivo in a Mouse Model of Nemaline Myopathy.

Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions.

Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions.

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