Cargando…

Huntington’s disease skeletal muscle has altered T-tubules

Romer et al. explored T-tubules in skeletal muscle.

Detalles Bibliográficos
Autores principales:	Khan, Muhammad S., Shaw, Robin M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Rockefeller University Press 2021
Materias:	Commentary
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8126974/ https://www.ncbi.nlm.nih.gov/pubmed/33978682 http://dx.doi.org/10.1085/jgp.202012843

Ejemplares similares

A mouse model of Huntington’s disease shows altered ultrastructure of transverse tubules in skeletal muscle fibers
por: Romer, Shannon H., et al.
Publicado: (2021)

Skeletal Muscle Modulates Huntington’s Disease Pathogenesis in Mice: Role of Physical Exercise
por: Corrochano, Silvia, et al.
Publicado: (2018)

Skeletal muscle pathology in Huntington's disease
por: Zielonka, Daniel, et al.
Publicado: (2014)

A shared mechanism of muscle wasting in cancer and Huntington’s disease
por: Mielcarek, Michal, et al.
Publicado: (2015)

Age-related mitochondrial alterations in brain and skeletal muscle of the YAC128 model of Huntington disease
por: Bečanović, Kristina, et al.
Publicado: (2021)

Trojan triplets: RNA-based pathomechanisms for muscle dysfunction in Huntington’s disease
por: Skov, Martin, et al.
Publicado: (2017)

THE LOCATION OF SODIUM IN THE TRANSVERSE TUBULES OF SKELETAL MUSCLE
por: Zadunaisky, Jose A.
Publicado: (1966)

Effects of Exercise on Skeletal Muscle Pathophysiology in Huntington’s Disease
por: Trovato, Bruno, et al.
Publicado: (2022)

SARCOPLASMIC RETICULUM AND T TUBULES IN DIFFERENTIATING RAT SKELETAL MUSCLE
por: Kelly, A. M.
Publicado: (1971)

Transcriptional Signature of an Altered Purine Metabolism in the Skeletal Muscle of a Huntington's Disease Mouse Model
por: Mielcarek, Michal, et al.
Publicado: (2017)

Author Correction: Age-related mitochondrial alterations in brain and skeletal muscle of the YAC128 model of Huntington disease
por: Bečanović, Kristina, et al.
Publicado: (2021)

T-tubule biogenesis and triad formation in skeletal muscle and implication in human diseases
por: Al-Qusairi, Lama, et al.
Publicado: (2011)

Rectifying rectifier channels in Huntington disease
por: Proft, Juliane, et al.
Publicado: (2014)

Cerebrospinal fluid levels of proenkephalin and prodynorphin are differentially altered in Huntington’s and Parkinson’s disease
por: Barschke, Peggy, et al.
Publicado: (2022)

Myostatin inhibition prevents skeletal muscle pathophysiology in Huntington’s disease mice
por: Bondulich, Marie K., et al.
Publicado: (2017)

Synaptopathy, circuitopathy and the computational biology of Huntington’s disease
por: Hannan, Anthony J.
Publicado: (2018)

Beyond the Glomerulus—Kidney Tubule Markers and Diabetic Kidney Disease Progression
por: Bullen, Alexander L., et al.
Publicado: (2021)

Anomalous ion diffusion within skeletal muscle transverse tubule networks
por: Shorten, Paul R, et al.
Publicado: (2007)

Action Potential in the Transverse Tubules and Its Role in the Activation of Skeletal Muscle
por: Bastian, Joseph, et al.
Publicado: (1974)

Dysferlin at transverse tubules regulates Ca(2+) homeostasis in skeletal muscle
por: Kerr, Jaclyn P., et al.
Publicado: (2014)

Rosiglitazone Ameliorates Cardiac and Skeletal Muscle Dysfunction by Correction of Energetics in Huntington’s Disease
por: Tomczyk, Marta, et al.
Publicado: (2022)

Phenotypic Variability in Huntington's Disease
por: Chouksey, Anjali, et al.
Publicado: (2020)

Renal proximal tubule cells: power and finesse
por: Fuchs, Michaela A.A., et al.
Publicado: (2023)

Implications of the Orb2 Amyloid Structure in Huntington’s Disease
por: Hervás, Rubén, et al.
Publicado: (2020)

Muscle specific iron deficiency has systemic consequences
por: Kaplan, Jerry, et al.
Publicado: (2015)

Altered Ca(2+) signaling in skeletal muscle fibers of the R6/2 mouse, a model of Huntington’s disease
por: Braubach, Peter, et al.
Publicado: (2014)

Effects of endurance training on skeletal muscle mitochondrial function in Huntington disease patients
por: Mueller, Sandro Manuel, et al.
Publicado: (2017)

Supporting Huntington’s Disease Families Through the Ups and Downs of Clinical Trials
por: Andrew, Kelly M., et al.
Publicado: (2023)

Protection of renal tubules against gentamicin induced nephrotoxicity
por: Tavafi, Majid
Publicado: (2013)

On the connection between the transverse tubules and the plasma membrane in frog semitendinosus skeletal muscle
por: Zampighi, G, et al.
Publicado: (1975)

Linear Electrical Properties of the Transverse Tubules and Surface Membrane of Skeletal Muscle Fibers
por: Schneider, Martin F.
Publicado: (1970)

Tuning in to the rhythm of clock genes in skeletal muscle()
por: Zhou, Zhou, et al.
Publicado: (2013)

Low Anaerobic Threshold and Increased Skeletal Muscle Lactate Production in Subjects with Huntington's Disease
por: Ciammola, Andrea, et al.
Publicado: (2011)

Compensation in the course of Huntington's disease — More than just a hypothesis?
por: Schiefer, Johannes
Publicado: (2015)

Neural Compensation in Huntington's Disease: Teaching Mental Disorders New Tricks?
por: Wolf, Robert Christian, et al.
Publicado: (2015)

Profile of pridopidine and its potential in the treatment of Huntington disease: the evidence to date
por: Squitieri, Ferdinando, et al.
Publicado: (2015)

Eps 15 Homology Domain (EHD)-1 Remodels Transverse Tubules in Skeletal Muscle
por: Demonbreun, Alexis R., et al.
Publicado: (2015)

Resurrection of sildenafil: potential for Huntington’s Disease, too?
por: Achenbach, Jannis, et al.
Publicado: (2022)

Insulin Resistance by Adiponectin Deficiency: Is the Action in Skeletal Muscle?
por: Karpe, Fredrik
Publicado: (2013)

The ins and outs of acid–base transport in skeletal muscle
por: Aalkjær, Christian, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_olmkghq7p60ivr61cp71ikmdoc