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GDAP1 encodes a member of the ganglioside-induced differentiation-associated protein family, which may play a role in a signal transduction pathway during neuronal development. De plus, nous expédions GDAP1 Protéines (5) et beaucoup plus de produits pour cette protéine.
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Human Polyclonal GDAP1 Primary Antibody pour ELISA, WB - ABIN565729
Cassereau, Chevrollier, Gueguen, Malinge, Letournel, Nicolas, Richard, Ferre, Verny, Dubas, Procaccio, Amati-Bonneau, Bonneau, Reynier: Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K). dans Neurogenetics 2009
Show all 3 references for ABIN565729
This study suggest GDAP1 as the first gene that should be analysed in Italian patients affected by CMT2.
study reports on 2 Charcot-Marie-Tooth (CMT) families in which a newly identified Glu222Lys mutation within the GDAP1 gene segregates both in autosomal dominant and recessive traits
The novelty of our data is the relatively high frequency of SH3TC2 (Montrer SH3TC2 Anticorps) and GDAP1 mutations in demyelinating and axonal forms, respectively, of Charcot-Marie-Tooth disease
Results show that JPH1 (Montrer JPH1 Anticorps) and GDAP1 share a common pathway and depend on each other; therefore, JPH1 (Montrer JPH1 Anticorps) can contribute to the phenotypical consequences of GDAP1 mutations.
GDAP1-associated polyneuropathy caused predominantly a mild and slowly progressive phenotype.
This studies suggest that the pathophysiology of GDAP1-related CMT neuropathies may be associated with abnormal distribution and movement of mitochondria throughout cytoskeleton towards the ER and subplasmalemmal microdomains.
GDAP1 regulates mitochondrial and peroxisomal fission by a similar mechanism.
A novel heterozygous missense mutation (Arg120Gly) in the GDAP1 gene co-segregates with the disease within the pedigree of an Italian Charcot-Marie-Tooth disease type 2 (CMT2) family.
This study suggested that the mutation of GDAP1 cased onion bulb-like formations of schwann cell in peripheral neuropathies.
A French family with Charcot-Marie-Tooth disease is related to simultaneous heterozygous MFN2 (Montrer MFN2 Anticorps) and GDAP1 mutations.
absence of GDAP1 induces a peripheral neuropathy with loss of motor neurons, mitochondrial defects and abnormal calcium homeostasis.
Members of the GDAP1 family are responsive and protective against stress associated with increased levels of oxidized glutathione.
Cell expression of Gdap1 in the nervous system and pathogenesis of Charcot-Marie-Tooth type 4A disease are reported.
This gene encodes a member of the ganglioside-induced differentiation-associated protein family, which may play a role in a signal transduction pathway during neuronal development. Mutations in this gene have been associated with various forms of Charcot-Marie-Tooth Disease and neuropathy. Two transcript variants encoding different isoforms and a noncoding variant have been identified for this gene.
ganglioside-induced differentiation-associated protein 1
, Charcot-Marie-Tooth neuropathy 4A
, ganglioside differentiation associated protein 1