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anti-Human MTM1 Anticorps:
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Human Polyclonal MTM1 Primary Antibody pour IHC (p), WB - ABIN1882103
Herman, Kopacz, Zhao, Mills, Metzenberg, Das: Characterization of mutations in fifty North American patients with X-linked myotubular myopathy. dans Human mutation 2002
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Human Polyclonal MTM1 Primary Antibody pour ICC, IF - ABIN4337571
Gupta, Hnia, Smith, Gundry, McIntire, Shimazu, Bass, Talbot, Amoasii, Goldman, Laporte, Beggs: Loss of catalytically inactive lipid phosphatase myotubularin-related protein 12 impairs myotubularin stability and promotes centronuclear myopathy in zebrafish. dans PLoS genetics 2013
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Human Polyclonal MTM1 Primary Antibody pour ELISA, WB - ABIN268752
Laporte, Hu, Kretz, Mandel, Kioschis, Coy, Klauck, Poustka, Dahl: A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast. dans Nature genetics 1996
Human Monoclonal MTM1 Primary Antibody pour IHC (p), RNAi - ABIN561867
Hedberg, Lindberg, Máthé, Moslemi, Oldfors: Myopathy in a woman and her daughter associated with a novel splice site MTM1 mutation. dans Neuromuscular disorders : NMD 2012
level of myotubes MTM1 mutations do not dramatically affect calcium homeostasis and calcium release mediated through the ryanodine receptor 1 (Montrer RYR1 Anticorps), though they do affect myotube size and nuclear content..mature muscles such as those obtained from patient muscle biopsies exhibit a significant decrease in expression of the ryanodine receptor 1 (Montrer RYR1 Anticorps), a decrease in muscle-specific (Montrer EIF3K Anticorps) microRNAs and a considerable up-regulation of HDAC4 (Montrer HDAC4 Anticorps).
In platelets, MTM1 is a highly active 3-phosphatase mainly associated to membranes and found on the dense granules and to a lesser (Montrer F2 Anticorps)extent on alpha-granules.
Results confirm that the severe neonatal onset of myopathy in male infants is sufficient to address the direct molecular testing toward the MTM1 gene and, above all, suggest that the number of undiagnosed symptomatic female carriers is probably underestimated
This study demonistrated that MTM1 mutation releated to Centronuclear myopathy.
mutations in SPEG (Montrer SPEG Anticorps) cause a centronuclear myopathy phenotype as a result of its interaction with MTM1.
Mutations in specific myotubularins such as MTM1 result in myotubular myopathy and Charcot-Marie-Tooth peripheral neuropathy. (Review)
Large duplications in MTM1 may account for a number of Centronuclear myopathy cases that have remained genetically unresolved.
Analysis of human XLMTM patient myotubes showed that mutations that disrupt the interaction between myotubularin and MTMR12 (Montrer MTMR12 Anticorps) proteins result in reduction of both myotubularin and MTMR12 (Montrer MTMR12 Anticorps)
data explain the basis for phenotypic variability among human patients with MTM1 p.R69C mutations and establish the Mtm1 p.R69C mouse as a valuable model for the disease, as its less severe phenotype will expand the scope of testable preclinical therapies
The patients of Myopathy had a novel heterozygous splice site mutation in the myotubularin gene, MTM1 (c.867+1G>T). Analysis of MTM1 cDNA revealed that the mutation resulted in aberrant splicing with variable exon skipping.
deletion of MTM1 in mouse had no significant effect on platelet count and on platelet secretion and aggregation induced by thrombin (Montrer F2 Anticorps) or collagen stimulation.
Differential muscle hypertrophy is associated with satellite cell numbers and Akt (Montrer AKT1 Anticorps) pathway activation following activin type IIB receptor (Montrer ACVR2B Anticorps) inhibition in Mtm1
MTM1 interacts with BIN1 (Montrer BIN1 Anticorps) in skeletal muscle.
Data show that the IGF1R (Montrer IGF1R Anticorps)/Akt (Montrer AKT1 Anticorps) pathway is affected in phosphoinositide phosphatase myotubularin (MTM1)-deficient muscles.
Deletion of the Mtm1 gene in a mature muscle reproduces the pathological hallmarks of myotubular myopathy.
study reveal a direct function of MTM1 enzymatic activity in SR remodeling and a key role for PtdIns3P in promoting SR membrane curvature in skeletal muscle.
aberrant mTORC1 signaling and impaired autophagy are consequences of the loss of Mtm1
Phosphatase-dead myotubularin ameliorates X-linked centronuclear myopathy phenotypes in mice.
These studies demonstrate specific abnormalities in myogenic cell number and behavior that may relate to the progression of disease in myotubularin deficiency.
This gene encodes a dual-specificity phosphatase that acts on both phosphotyrosine and phosphoserine. It is required for muscle cell differentiation and mutations in this gene have been identified as being responsible for X-linked myotubular myopathy.
, X-linked myotubular myopathy gene 1