VB
Vivien Béziat
Inserm, Rockefeller University
Research areas: Immunology and Microbiology · Immunology · Immunodeficiency and Autoimmune Disorders · Immune Cell Function and Interaction · T-cell and B-cell Immunology
0000-0002-4020-824X
Employment
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INSERM Directeur de recherche de classe 22024 - Present
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Rockefeller University Guest Investigator2018 - Present
Education
Education history is unavailable.
Projects & Funding
Projects & funding information is unavailable.
Publications (138)
- CD28-deficient mice are vulnerable to mouse papillomavirus MmuPV1 infection of the skin and mucosae. Save
- Human LFA-1 governs T cell immune surveillance of the skin. Save
- Genotype-phenotype correlations and cancer risk in monogenic epidermodysplasia verruciformis. Save
- Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function. Save
- Monogenic disorders of immunity: Common variants are not so rare. Save
- Genotypes truncating the intracellular tail of human pre-TCRα: From amorphic to isomorphic. Save
- Dupilumab in atopic-dermatitis-like eczema associated with inborn errors of immunity: A nationwide study Save
- Inborn errors of immunity reveal molecular requirements for generation and maintenance of human CD4+ IL-9-expressing cells Save
- Inherited IL-18BP deficiency in two Egyptian siblings with fulminant viral hepatitis Save
- Serological diagnosis of chronic skin granulomas caused by wild-type or vaccine-derived rubella virus in patients with inherited HLA class I deficiency Save
- The monogenic landscape of human infectious diseases Save
- Two different forms of inherited human TCRα chain deficiency Save
- Case Report of Two Independent Moroccan Families with Syndromic Epidermodysplasia Verruciformis and STK4 Deficiency Save
- A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunity Save
- A sensitive assay for measuring whole- blood responses to type I IFNs Save
- Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activation Save
- FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice Save
- Gain-of-function human UNC93B1 variants cause systemic lupus erythematosus and chilblain lupus Save
- Helper T cell immunity in humans with inherited CD4 deficiency Save
- Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children Save