Vivien Béziat
Béziat, Vivien 1984-...
VIAF ID: 173108883 (Personal)
Permalink: http://viaf.org/viaf/173108883
Preferred Forms
- 100 1 _ ‡a Béziat, Vivien, ‡d 1984-....
- 100 1 _ ‡a Béziat, Vivien ‡d 1984-...
- 100 0 _ ‡a Vivien Béziat
4xx's: Alternate Name Forms (3)
Works
Title | Sources |
---|---|
Accumulation of Intrahepatic TNF-α-Producing NKp44+ NK Cells Correlates With Liver Fibrosis and Viral Load in Chronic HCV Infection | |
Candidate Predisposition Variants in Kaposi Sarcoma as Detected by Whole-Genome Sequencing | |
CD56brightCD16+ NK cells: a functional intermediate stage of NK cell differentiation | |
CD8 T cells express randomly selected KIRs with distinct specificities compared with NK cells | |
Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β | |
Class I HLA haplotypes form two schools that educate NK cells in different ways | |
Cognate HLA absence in trans diminishes human NK cell education | |
Coordinated expression of DNAM-1 and LFA-1 in educated NK cells | |
Correction: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome | |
Critical Role of CD2 Co-stimulation in Adaptive Natural Killer Cell Responses Revealed in NKG2C-Deficient Humans. | |
Cutting edge: identification and characterization of human intrahepatic CD49a+ NK cells. | |
Cytomegalovirus infection drives adaptive epigenetic diversification of NK cells with altered signaling and effector function | |
Deciphering the killer-cell immunoglobulin-like receptor system at super-resolution for natural killer and T-cell biology | |
Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders | |
Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations. | |
Effectiveness and safety of ruxolitinib for the treatment of refractory systemic idiopathic juvenile arthritis like associated with interstitial lung disease : a case report | |
Effects of HDV infection and pegylated interferon α treatment on the natural killer cell compartment in chronically infected individuals | |
Efficacy of Dupilumab for Controlling Severe Atopic Dermatitis in a Patient with Hyper-IgE Syndrome | |
Etude de la différenciation terminale des cellules NK basée sur différents modèles cliniques : rôle du CD16, NKG2A, NKG2C et des KIRs | |
Fatal Cytomegalovirus Infection in an Adult with Inherited NOS2 Deficiency | |
Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency | |
Harnessing adaptive natural killer cells in cancer immunotherapy | |
Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency | |
HLA-E upregulation on IFN-γ-activated AML blasts impairs CD94/NKG2A-dependent NK cytolysis after haplo-mismatched hematopoietic SCT | |
A homozygous mutation of RTEL1 in a child presenting with an apparently isolated natural killer cell deficiency. | |
Homozygous NLRP1 gain-of-function mutation in siblings with a syndromic form of recurrent respiratory papillomatosis | |
Human genetic dissection of papillomavirus-driven diseases: new insight into their pathogenesis | |
Human hyper-IgE syndrome: singular or plural? | |
Human inborn errors of immunity to herpes viruses | |
Human NK cells display major phenotypic and functional changes over the life span | |
Human NKG2A overrides NKG2C effector functions to prevent autoreactivity of NK cells | |
The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants | |
Inborn errors of the development of human natural killer cells | |
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19 | |
Independent skewing of the T cell and NK cell compartments associated with cytomegalovirus infection suggests division of labor between innate and adaptive immunity. | |
Influence of KIR gene copy number on natural killer cell education | |
Inherited IL-18BP deficiency in human fulminant viral hepatitis. | |
Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child | |
IRF4 haploinsufficiency in a family with Whipple's disease. | |
A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes | |
Naive Donor NK Cell Repertoires Associated with Less Leukemia Relapse after Allogeneic Hematopoietic Stem Cell Transplantation. | |
Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance | |
NK cell terminal differentiation: correlated stepwise decrease of NKG2A and acquisition of KIRs | |
Phenotype and function of natural killer cells in systemic lupus erythematosus: Excess interferon-γ production in patients with active disease | |
Polyclonal Expansion of NKG2C(+) NK Cells in TAP-Deficient Patients | |
Recalcitrant Warts, Epidermodysplasia Verruciformis, and the Tree-Man Syndrome: Phenotypic Spectrum of Cutaneous Human Papillomavirus Infections at the Intersection of Genetic Variability of Viral and Human Genomes | |
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity | |
The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies | |
Role for early-differentiated natural killer cells in infectious mononucleosis | |
Role of natural killer cells in hematopoietic stem cell transplantation: myth or reality? | |
Shaping of iNKT cell repertoire after unrelated cord blood transplantation. | |
Specificity and dynamics of effector and memory CD8 T cell responses in human tick-borne encephalitis virus infection | |
Spotlight on NKG2C and the human NK-cell response to CMV infection | |
Tracing dynamic expansion of human NK-cell subsets by high-resolution analysis of KIR repertoires and cellular differentiation | |
Unconventional repertoire profile is imprinted during acute chikungunya infection for natural killer cells polarization toward cytotoxicity | |
ZNF341 controls STAT3 expression and thereby immunocompetence |