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Human genetic dissection of papillomavirus-driven diseases: new insight into their pathogenesis

Human genetics, 2020-06, Vol.139 (6-7), p.919-939

Béziat, Vivien

2020

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Human inborn errors of immunity to oncogenic viruses

Current opinion in immunology, 2021-10, Vol.72, p.277-285

2021

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The “Editors” Take to RAG: Promise of CRISPR/Cas9/rAAV6-Based Gene Therapy for RAG2 Deficiency

Journal of clinical immunology, 2021-07, Vol.41 (5), p.849-851

2021

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Human inborn errors of immunity to herpes viruses

Current opinion in immunology, 2020-02, Vol.62, p.106-122

2020

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NK cell terminal differentiation: correlated stepwise decrease of NKG2A and acquisition of KIRs

PloS one, 2010-08, Vol.5 (8), p.e11966-e11966

2010

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The Pathogenesis of Giant Condyloma Acuminatum (Buschke-Lowenstein Tumor): An Overview

International journal of molecular sciences, 2022-04, Vol.23 (9), p.4547

2022

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Dominant negative CARD11 mutations: Beyond atopy

Journal of allergy and clinical immunology, 2019-04, Vol.143 (4), p.1345-1347

2019

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Unconventional repertoire profile is imprinted during acute chikungunya infection for natural killer cells polarization toward cytotoxicity

PLoS pathogens, 2011-09, Vol.7 (9), p.e1002268-e1002268

2011

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Effectiveness and safety of ruxolitinib for the treatment of refractory systemic idiopathic juvenile arthritis like associated with interstitial lung disease : a case report

Annals of the rheumatic diseases, 2022-02, Vol.81 (2), p.e20-e20

2022

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Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance

Proceedings of the National Academy of Sciences - PNAS, 2021-01, Vol.118 (3), p.1

2021

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Human hyper-IgE syndrome: singular or plural?

Mammalian genome, 2018-08, Vol.29 (7-8), p.603-617

2018

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Inherited human ZNF341 deficiency

Current opinion in immunology, 2023-06, Vol.82, p.102326-102326, Article 102326

2023

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Human NK cells display major phenotypic and functional changes over the life span

Aging cell, 2010-08, Vol.9 (4), p.527-535

2010

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Human genetic and immunological dissection of papillomavirus-driven diseases: new insights into their pathogenesis

Current opinion in virology, 2021-12, Vol.51, p.9-15

2021

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Deciphering the killer‐cell immunoglobulin‐like receptor system at super‐resolution for natural killer and T‐cell biology

Immunology, 2017-03, Vol.150 (3), p.248-264

2017

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A homozygous mutation of RTEL1 in a child presenting with an apparently isolated natural killer cell deficiency

Journal of allergy and clinical immunology, 2015-10, Vol.136 (4), p.1113-1114

2015

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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

Journal of investigative dermatology, 2022-05, Vol.142 (5), p.1265-1269

2022

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Hyperimmunoglobulinémie E et Déficits Immunitaires Héréditaires

Tunisie Medicale, 2023-12, Vol.101 (12), p.862-870

2023

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Tracing dynamic expansion of human NK‐cell subsets by high‐resolution analysis of KIR repertoires and cellular differentiation

European journal of immunology, 2014-07, Vol.44 (7), p.2192-2196

2014

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HPV-Related Skin Phenotypes in Patients with Inborn Errors of Immunity

Pathogens (Basel), 2022-07, Vol.11 (8), p.857

2022

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Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders

Orphanet journal of rare diseases, 2018-08, Vol.13 (1), p.139-139, Article 139

2018

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Whole-Transcriptome Sequencing–Based Profiling of the Cutaneous Virome in Patients with Secondary Immunodeficiency

JID innovations, 2024-07, Vol.4 (4), p.100278, Article 100278

2024

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Cutting edge: identification and characterization of human intrahepatic CD49a+ NK cells

The Journal of immunology (1950), 2015-03, Vol.194 (6), p.2467-2471

2015

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Inherited IL-18BP deficiency in human fulminant viral hepatitis

The Journal of experimental medicine, 2019-08, Vol.216 (8), p.1777-1790

2019

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Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome

Journal of clinical immunology, 2022-04, Vol.42 (3), p.471-483

2022

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Human genetic dissection of papillomavirus-driven diseases: new insight into their pathogenesis

Human inborn errors of immunity to oncogenic viruses

The “Editors” Take to RAG: Promise of CRISPR/Cas9/rAAV6-Based Gene Therapy for RAG2 Deficiency

Human inborn errors of immunity to herpes viruses

NK cell terminal differentiation: correlated stepwise decrease of NKG2A and acquisition of KIRs

The Pathogenesis of Giant Condyloma Acuminatum (Buschke-Lowenstein Tumor): An Overview

Dominant negative CARD11 mutations: Beyond atopy

Unconventional repertoire profile is imprinted during acute chikungunya infection for natural killer cells polarization toward cytotoxicity

Effectiveness and safety of ruxolitinib for the treatment of refractory systemic idiopathic juvenile arthritis like associated with interstitial lung disease : a case report

Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance

Human hyper-IgE syndrome: singular or plural?

Inherited human ZNF341 deficiency

Human NK cells display major phenotypic and functional changes over the life span

Human genetic and immunological dissection of papillomavirus-driven diseases: new insights into their pathogenesis

Deciphering the killer‐cell immunoglobulin‐like receptor system at super‐resolution for natural killer and T‐cell biology

A homozygous mutation of RTEL1 in a child presenting with an apparently isolated natural killer cell deficiency

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

Hyperimmunoglobulinémie E et Déficits Immunitaires Héréditaires

Tracing dynamic expansion of human NK‐cell subsets by high‐resolution analysis of KIR repertoires and cellular differentiation

HPV-Related Skin Phenotypes in Patients with Inborn Errors of Immunity

Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders

Whole-Transcriptome Sequencing–Based Profiling of the Cutaneous Virome in Patients with Secondary Immunodeficiency

Cutting edge: identification and characterization of human intrahepatic CD49a+ NK cells

Inherited IL-18BP deficiency in human fulminant viral hepatitis

Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome

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