Chavanas, Stéphane
Stephane Chavanas
VIAF ID: 197878581 (Personal)
Permalink: http://viaf.org/viaf/197878581
Preferred Forms
- 100 1 _ ‡a Chavanas, Stéphane
- 100 1 _ ‡a Chavanas, Stéphane
- 100 0 _ ‡a Stephane Chavanas
4xx's: Alternate Name Forms (2)
Works
Title | Sources |
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Comprehensive analysis of human cytomegalovirus microRNA expression during lytic and quiescent infection. | |
Cytomegalovirus Infection Triggers the Secretion of the PPARγ Agonists 15-Hydroxyeicosatetraenoic Acid (15-HETE) and 13-Hydroxyoctadecadienoic Acid (13-HODE) in Human Cytotrophoblasts and Placental Cultures. | |
Développement et validation d'un modèle cellulaire de kératopathie associée à l'aniridie | |
Gene polymorphism in Netherton and common atopic disease | |
Genotype-phenotype relations in hereditary epidermolysis bullosa : importance of the post-transcriptional regulation of the aberrant rnas. | |
Human Cytomegalovirus Infection Dysregulates the Localization and Stability of NICD1 and Jag1 in Neural Progenitor Cells. | |
Immuno-virologic determinants of congenital cytomegalovirus infection in peripheral fetal samples and brain tissue. | |
In vitro modeling of aniridia-related keratopathy and its validation. | |
Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping. | |
Long-range enhancer differentially regulated by c-Jun and JunD controls peptidylarginine deiminase-3 gene in keratinocytes. | |
MicroRNA miR-21 attenuates human cytomegalovirus replication in neural cells by targeting Cdc25a. | |
Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families | |
A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin. | |
Peroxisome proliferator-activated receptor γ (PPARγ) activation: A key determinant of neuropathogeny during congenital infection by cytomegalovirus. | |
Physiopathologie de l'infection par le cytomégalovirus sur les progéniteurs neuraux humains | |
PPAR Gamma and Viral Infections of the Brain | |
Regulation of the expression of peptidylarginine deiminase type II gene (PADI2) in human keratinocytes involves Sp1 and Sp3 transcription factors. | |
Role of the bullous pemphigoid antigen 180 (BP180) in the assembly of hemidesmosomes and cell adhesion--reexpression of BP180 in generalized atrophic benign epidermolysis bullosa keratinocytes. | |
Update on peptidylarginine deiminases and deimination in skin physiology and severe human diseases. |