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TranscriptomicsExpression data from Gdap1 knock-out (deletion of exon 5) mice
GDAP1 is a mitochondrial fission factor and mutations in GDAP1 cause Charcot-Marie-Tooth disease. Gdap1 knockout mice, mimicking genetic alterations of patients suffering from severe CMT forms, develop an age-related, hypomyelinating peripheral neuropathy. We used microarrays to determine changes in...
ORGANISM(S): Mus musculus 
2014-01-03 | E-GEOD-51650 | biostudies-arrayexpress
Proteomics1GDAP1 loss of function inhibits the mitochondrial pyruvate dehydrogenase complex by altering the actin cytoskeleton
Charcot-Marie-Tooth (CMT) disease 4A is an autosomal-recessive polyneuropathy caused by mutations of ganglioside-induced differentiation-associated protein 1 (GDAP1), a putative glutathione transferase, which affects mitochondrial shape and alters cellular Ca2+homeostasis. Here, w...
ORGANISM(S): Mus musculus (Mouse) 
2022-08-12 | PXD024555 | Pride
Mouse Gdap1 Pulldown Sp3 Lc-udmse Primary cortical neurons 
ProteomicsGDAP1 loss of function inhibits the mitochondrial pyruvate dehydrogenase complex by altering the actin cytoskeleton
Charcot-Marie-Tooth (CMT) disease 4A is an autosomal-recessive polyneuropathy caused by mutations of ganglioside-induced differentiation-associated protein 1 (GDAP1), a putative glutathione transferase, which affects mitochondrial shape and alters cellular Ca2+ homeostasis. Here, we identify the und...
ORGANISM(S): Homo sapiens (Human) 
2022-08-12 | PXD028460 | Pride
Β-oxidation Lc-ms Gdap1 
TranscriptomicsExpression data from wild type or Gdap1-null Mouse Embryonic Fibroblasts
Expression data from wild type or Gdap1-null Mouse Embryonic Fibroblasts before and 4 days after transduction with the reprogramming factors Oct4, Sox2, Klf4 and cMyc We used microarrays to detail the global programme of gene expression underlying cell reprogramming Total RNA from wild type or Gdap1...
ORGANISM(S): Mus musculus 
2016-03-01 | E-GEOD-59527 | biostudies-arrayexpress
TranscriptomicsExpression data from Gdap1 knock-out (deletion of exon 5) mice
GDAP1 is a mitochondrial fission factor and mutations in GDAP1 cause Charcot-Marie-Tooth disease. Gdap1 knockout mice, mimicking genetic alterations of patients suffering from severe CMT forms, develop an age-related, hypomyelinating peripheral neuropathy. We used microarrays to determine changes in...
ORGANISM(S): Mus musculus 
2014-01-03 | GSE51650 | GEO
UnknownDominant GDAP1 mutations cause predominantly mild CMT phenotypes.
Not available
S-EPMC3272385 | biostudies-literature
UnknownEpigenetic regulation of the human GDAP1 gene.
Not available
S-EPMC11426145 | biostudies-literature
TranscriptomicsExpression data from wild type or Gdap1-null Mouse Embryonic Fibroblasts
Expression data from wild type or Gdap1-null Mouse Embryonic Fibroblasts before and 4 days after transduction with the reprogramming factors Oct4, Sox2, Klf4 and cMyc We used microarrays to detail the global programme of gene expression underlying cell reprogramming
ORGANISM(S): Mus musculus 
2016-03-01 | GSE59527 | GEO
UnknownStructural and functional divergence of GDAP1 from the glutathione S-transferase superfamily.
Not available
S-EPMC9394736 | biostudies-literature
GenomicsMus musculus
Expression data from Gdap1 knock-out (deletion of exon 5) mice
PRJNA224198 | ENA
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