Apoptotic phenotype induced by overexpression of wild-type gas3/PMP22: its relation to the demyelinating peripheral neuropathy CMT1A.
about
gas7: A gene expressed preferentially in growth-arrested fibroblasts and terminally differentiated Purkinje neurons affects neurite formationPERP, an apoptosis-associated target of p53, is a novel member of the PMP-22/gas3 familyThe tetraspan protein epithelial membrane protein-2 interacts with beta1 integrins and regulates adhesionIsolation and properties of Gas8, a growth arrest-specific gene regulated during male gametogenesis to produce a protein associated with the sperm motility apparatusMicrofilament reorganization during apoptosis: the role of Gas2, a possible substrate for ICE-like proteasesGas7 functions with N-WASP to regulate the neurite outgrowth of hippocampal neurons.Overview of hereditary neuropathy with liability to pressure palsies.The anatomy and cell biology of peripheral myelin protein-22.New vistas on the pathomechanism of Charcot-Marie-Tooth and related peripheral neuropathies.Distinct phenotypes associated with increasing dosage of the PLP gene: implications for CMT1A due to PMP22 gene duplication.Transgenic mouse models of CMT1A and HNPP.The "CMT rat": peripheral neuropathy and dysmyelination caused by transgenic overexpression of PMP22.Tissue-specific Bcl-2 protein partners in apoptosis: An ovarian paradigm.Bax-mediated cell death by the Gax homeoprotein requires mitogen activation but is independent of cell cycle activityAnalysis of gene expression profile induced by EMP-1 in esophageal cancer cells using cDNA Microarray.The PMP22 gene and its related diseases.PMP22 is critical for actin-mediated cellular functions and for establishing lipid rafts.Genetic aspects of Charcot-Marie-Tooth disease.A proline-rich motif in p53 is required for transactivation-independent growth arrest as induced by Gas1.Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy.Pathomechanisms of mutant proteins in Charcot-Marie-Tooth disease.The palmitoylation state of PMP22 modulates epithelial cell morphology and migrationKinetic analysis of genomewide gene expression reveals molecule circuitries that control T cell activation and Th1/2 differentiation.Unscrambling the genomic chaos of osteosarcoma reveals extensive transcript fusion, recurrent rearrangements and frequent novel TP53 aberrationsEMP3 as a candidate tumor suppressor gene for solid tumors.Review of the GAS3 Family of Proteins and their Relevance to Cancer.Exposure at the cell surface is required for gas3/PMP22 To regulate both cell death and cell spreading: implication for the Charcot-Marie-Tooth type 1A and Dejerine-Sottas diseases.Rho-dependent regulation of cell spreading by the tetraspan membrane protein Gas3/PMP22.Acquired resistance to metformin in breast cancer cells triggers transcriptome reprogramming toward a degradome-related metastatic stem-like profile.The tmp gene, encoding a membrane protein, is a c-Myc target with a tumorigenic activityGas1-induced growth suppression requires a transactivation-independent p53 function.Expression analysis of PMP22/Gas3 in premalignant and malignant pancreatic lesions.Alternative Splicing in the Human PMP22 Gene: Implications in CMT1A Neuropathy.Modulation of epithelial morphology, monolayer permeability, and cell migration by growth arrest specific 3/peripheral myelin protein 22Glycan-independent role of calnexin in the intracellular retention of Charcot-Marie-tooth 1A Gas3/PMP22 mutants.Identification of a positive regulatory element in the myelin-specific promoter of the PMP22 gene.Post-transcriptional regulation of the peripheral myelin protein gene PMP22/gas3.The growth arrest genes gas5, gas6, and CHOP-10 (gadd153) are expressed in the mouse preimplantation embryo.Effects of nutrient deprivation and differentiation on the expression of growth-arrest genes (gas and gadd) in F9 embryonal carcinoma cells.Mutation analysis of the MPZ and PMP22 genes in Croatian patients.
P2860
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P2860
Apoptotic phenotype induced by overexpression of wild-type gas3/PMP22: its relation to the demyelinating peripheral neuropathy CMT1A.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Apoptotic phenotype induced by ...... g peripheral neuropathy CMT1A.
@en
Apoptotic phenotype induced by ...... g peripheral neuropathy CMT1A.
@nl
type
label
Apoptotic phenotype induced by ...... g peripheral neuropathy CMT1A.
@en
Apoptotic phenotype induced by ...... g peripheral neuropathy CMT1A.
@nl
prefLabel
Apoptotic phenotype induced by ...... g peripheral neuropathy CMT1A.
@en
Apoptotic phenotype induced by ...... g peripheral neuropathy CMT1A.
@nl
P2093
P356
P1433
P1476
Apoptotic phenotype induced by ...... ng peripheral neuropathy CMT1A
@en
P2093
P304
P356
10.1101/GAD.9.15.1846
P577
1995-08-01T00:00:00Z