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Stéphane Chavanas | doi.page

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Stéphane Chavanas

Inserm(FR)Université Fédérale de Toulouse Midi-Pyrénées(FR)

Publications by Year

Research Areas

Skin and Cellular Biology Research, Cytomegalovirus and herpesvirus research, NF-κB Signaling Pathways, Cell Adhesion Molecules Research, RNA regulation and disease

Most-Cited Works

→ Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome(2000)842 cited
→ Gene polymorphism in Netherton and common atopic disease(2001)395 cited
→ Defective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophy.(1996)229 cited
→ Bacteria-derived long chain fatty acid exhibits anti-inflammatory properties in colitis(2020)215 cited
→ Netherton Syndrome: Disease Expression and Spectrum of SPINK5 Mutations in 21 Families(2002)212 cited
→ Comparative analysis of the mouse and human peptidylarginine deiminase gene clusters reveals highly conserved non-coding segments and a new human gene, PADI6(2004)190 cited
→

The Spectrum of Pathogenic Mutations in SPINK5 in 19 Families with Netherton Syndrome: Implications for Mutation Detection and First Case of Prenatal Diagnosis

(2001)

162 cited

→ Peptidylarginine Deiminase Isoforms 1–3 Are Expressed in the Epidermis and Involved in the Deimination of K1 and Filaggrin(2005)147 cited

→ Localization of the Netherton Syndrome Gene to Chromosome 5q32, by Linkage Analysis and Homozygosity Mapping(2000)131 cited

→ A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophy.(1996)96 cited