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Defective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophyDeficient expression of aldehyde dehydrogenase 1A1 is consistent with increased sensitivity of Gorlin syndrome patients to radiation carcinogenesisBasal Cell Carcinoma in Gorlin's Patients: a Matter of Fibroblasts-Led Protumoral Microenvironment?Heterogeneity of the high molecular weight tau proteins in N115 neuroblastoma cells.Genetic correction of stem cells in the treatment of inherited diseases and focus on xeroderma pigmentosum.Dominant-negative effects of COL7A1 mutations can be rescued by controlled overexpression of normal collagen VII.Seven mammalian aminoacyl-tRNA synthetases co-purified as high molecular weight entities are associated within the same complex.High molecular weight tau distribution and microtubule stability in neuroblastoma N115 cells.Hemidesmosome assembly assessed by expression of a wild-type integrin beta 4 cDNA in junctional epidermolysis bullosa keratinocytes.Genetic bases of severe junctional epidermolysis bullosa presenting spontaneous amelioration with aging.Construction of skin equivalents for gene therapy of recessive dystrophic epidermolysis bullosa.[Characterization of a canine model of dystrophic bullous epidermolysis (DBE). Development of a gene therapy protocol].Rapid decay of alpha6 integrin caused by a mis-sense mutation in the propeller domain results in severe junctional epidermolysis bullosa with pyloric atresia.Functional correction of type VII collagen expression in dystrophic epidermolysis bullosa.Genetic correction of canine dystrophic epidermolysis bullosa mediated by retroviral vectors.Correction of dog dystrophic epidermolysis bullosa by transplantation of genetically modified epidermal autografts.A tau-related protein of 130 kDa is present in Alzheimer brain.Protein TAU variants present in paired helical filaments (PHFs) of Alzheimer brains.Absence of the Integrin α3 Subunit Induces an Activated Phenotype in Human KeratinocytesA Novel Homozygous Mutation Affecting Integrin α6 in a Case of Junctional Epidermolysis Bullosa with Pyloric Atresia Detected In Utero by Ultrasound ExaminationProperties of two isoforms of human blood platelet alpha-actinin[High molecular weight tau proteins and acquisition of neuronal polarity in peripheral nervous system]Polymorphism of alpha-actinin from human blood platelets. Homodimeric and heterodimeric formsSusceptibility of platelet alpha-actinin to a Ca2+-activated neutral protease
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description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Yannick Gache
@ast
Yannick Gache
@en
Yannick Gache
@es
Yannick Gache
@nl
Yannick Gache
@sl
type
label
Yannick Gache
@ast
Yannick Gache
@en
Yannick Gache
@es
Yannick Gache
@nl
Yannick Gache
@sl
prefLabel
Yannick Gache
@ast
Yannick Gache
@en
Yannick Gache
@es
Yannick Gache
@nl
Yannick Gache
@sl
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P21
P31
P496
0000-0002-5638-4854