Survival motor neuron protein deficiency impairs myotube formation by altering myogenic gene expression and focal adhesion dynamics. - Wikidata - wikimedia - TriplyDB

Survival motor neuron protein deficiency impairs myotube formation by altering myogenic gene expression and focal adhesion dynamics.

Survival motor neuron protein deficiency impairs myotube formation by altering myogenic gene expression and focal adhesion dynamics.

http://www.wikidata.org/entity/Q34074474

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Immune dysregulation may contribute to disease pathogenesis in spinal muscular atrophy mice ROCK inhibition as a therapy for spinal muscular atrophy: understanding the repercussions on multiple cellular targets Spinal muscular atrophy: from tissue specificity to therapeutic strategies SMN Protein Can Be Reliably Measured in Whole Blood with an Electrochemiluminescence (ECL) Immunoassay: Implications for Clinical Trials Low levels of Survival Motor Neuron protein are sufficient for normal muscle function in the SMNΔ7 mouse model of SMA.Activin Receptor Type IIB Inhibition Improves Muscle Phenotype and Function in a Mouse Model of Spinal Muscular Atrophy Chronic Treatment with the AMPK Agonist AICAR Prevents Skeletal Muscle Pathology but Fails to Improve Clinical Outcome in a Mouse Model of Severe Spinal Muscular Atrophy.Impaired Muscle Mitochondrial Biogenesis and Myogenesis in Spinal Muscular Atrophy.The Power of Human Protective Modifiers: PLS3 and CORO1C Unravel Impaired Endocytosis in Spinal Muscular Atrophy and Rescue SMA Phenotype Altered Levels of MicroRNA-9, -206, and -132 in Spinal Muscular Atrophy and Their Response to Antisense Oligonucleotide Therapy Advances in understanding the role of disease-associated proteins in spinal muscular atrophy.SMN deficiency does not induce oxidative stress in SMA iPSC-derived astrocytes or motor neurons.Differential induction of muscle atrophy pathways in two mouse models of spinal muscular atrophy.Single-Blind, Randomized, Controlled Clinical Trial of Exercise in Ambulatory Spinal Muscular Atrophy: Why are the Results Negative?miRNA in spinal muscular atrophy pathogenesis and therapy.Increasing Agrin Function Antagonizes Muscle Atrophy and Motor Impairment in Spinal Muscular Atrophy.Small-molecule flunarizine increases SMN protein in nuclear Cajal bodies and motor function in a mouse model of spinal muscular atrophy.Interventions Targeting Glucocorticoid-Krüppel-like Factor 15-Branched-Chain Amino Acid Signaling Improve Disease Phenotypes in Spinal Muscular Atrophy Mice.Light modulation ameliorates expression of circadian genes and disease progression in spinal muscular atrophy mice

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P2860

Survival motor neuron protein deficiency impairs myotube formation by altering myogenic gene expression and focal adhesion dynamics.

http://www.wikidata.org/entity/Q34074474

description

2014 nî lūn-bûn

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2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2014 թվականի ապրիլին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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Survival motor neuron protein ...... n and focal adhesion dynamics.

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Survival motor neuron protein ...... n and focal adhesion dynamics.

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Survival motor neuron protein ...... n and focal adhesion dynamics.

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Survival motor neuron protein ...... n and focal adhesion dynamics.

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Survival motor neuron protein ...... n and focal adhesion dynamics.

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Survival motor neuron protein ...... n and focal adhesion dynamics.

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Survival motor neuron protein ...... n and focal adhesion dynamics.

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Survival motor neuron protein ...... n and focal adhesion dynamics.

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Human Molecular Genetics

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Survival motor neuron protein ...... n and focal adhesion dynamics.

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Barrington G Burnett

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Charlotte J Sumner

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Evgenia Leikina

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Katherine V Bricceno

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Kenneth H Fischbeck

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Leonid V Chernomordik

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Tara Martinez

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Terence A Partridge

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P2860

Modeling spinal muscular atrophy in Drosophila

Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophy.

Regulation of SMN protein stability

Spatial distribution and functional significance of activated vinculin in living cells

Identification and characterization of a spinal muscular atrophy-determining gene

Regulation of actin assembly associated with protrusion and adhesion in cell migration

Differences and similarities in DNA-binding preferences of MyoD and E2A protein complexes revealed by binding site selection

Integrins in cell migration

miR-206 and -486 induce myoblast differentiation by downregulating Pax7

Extracellular annexins and dynamin are important for sequential steps in myoblast fusion.

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10.1093/HMG/DDU189

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18

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23

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Stephanie Duguez

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2014-04-23T00:00:00Z

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261840351

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4140458

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