about
A1152D mutation of the Na+ channel causes paramyotonia congenita and emphasizes the role of DIII/S4-S5 linker in fast inactivationAssignment of the human TAFII30 gene (TAF2H) to human chromosome band 11p15.3 using somatic cell hybridsFrench myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertionPotential role of IL-17-producing iNKT cells in type 1 diabetes.Myotonic dystrophy: size- and sex-dependent dynamics of CTG meiotic instability, and somatic mosaicism.Single insulin-specific CD8+ T cells show characteristic gene expression profiles in human type 1 diabetes.HLA-B7-restricted islet epitopes are differentially recognized in type 1 diabetic children and adults and form weak peptide-HLA complexes.Recognition of human proinsulin leader sequence by class I-restricted T-cells in HLA-A*0201 transgenic mice and in human type 1 diabetes.The targeting of β-cells by T lymphocytes in human type 1 diabetes: clinical perspectives.Materno-Fetal Transfer of Preproinsulin Through the Neonatal Fc Receptor Prevents Autoimmune Diabetes.Detection of an EcoRI restriction fragment length polymorphism in the gene encoding the human TBP associated factor II 30 (TAF(II)30)Gating defects of a novel Na+ channel mutant causing hypokalemic periodic paralysisHumanized Mouse Model to Study Type 1 Diabetes
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Sandrine Luce
@ast
Sandrine Luce
@en
Sandrine Luce
@es
Sandrine Luce
@nl
type
label
Sandrine Luce
@ast
Sandrine Luce
@en
Sandrine Luce
@es
Sandrine Luce
@nl
prefLabel
Sandrine Luce
@ast
Sandrine Luce
@en
Sandrine Luce
@es
Sandrine Luce
@nl
P106
P21
P31
P496
0000-0002-9519-333X