Anne Puel chercheuse
Puel, Anne
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
VIAF ID: 304446186 (Personal)
Permalink: http://viaf.org/viaf/304446186
Preferred Forms
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Anne Puel
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chercheuse
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PUEL, ANNE.
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100 1 _
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Puel, Anne
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100 1 _
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Puel, Anne
4xx's: Alternate Name Forms (3)
Works
| Title | Sources |
|---|---|
| ETUDE DE LA REGULATION GENETIQUE QUANTITATIVE DE LA PRODUCTION D'ANTICORPS CHEZ LA SOURIS |
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| A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency |
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| Identification et caractérisation des bases génétiques moléculaires responsables de la prédisposition à la candidose cutanéo-muqueuse chronique chez l'homme |
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| IgM+IgD+CD27+ B cells are markedly reduced in IRAK-4-, MyD88-, and TIRAP- but not UNC-93B-deficient patients |
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| Immunity to infection in IL-17-deficient mice and humans |
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| Inborn errors of interferon (IFN)-mediated immunity in humans: insights into the respective roles of IFN-alpha/beta, IFN-gamma, and IFN-lambda in host defense |
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| Inborn errors of mucocutaneous immunity to Candida albicans in humans: a role for IL-17 cytokines? |
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| Inborn errors of type I IFN immunity in patients with life-threatening COVID-19 |
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| Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated exons |
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| Infections fongiques invasives et déficit en CARD9. |
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| Infectious diseases in patients with IRAK-4, MyD88, NEMO, or IκBα deficiency |
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| Inherited CARD9 Deficiency in a Patient with Both Exophiala spinifera and Aspergillus nomius Severe Infections |
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| Inherited CARD9 deficiency in otherwise healthy children and adults with Candida species-induced meningoencephalitis, colitis, or both |
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| Inherited disorders of human Toll-like receptor signaling: immunological implications. |
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| Inherited human IRAK-4 deficiency: an update. |
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| Intéractions hôte-pathogène dans l'infection par Mycobacterium tuberculosis : rôle des cellules dentritiques et des lymphocytes T doubles positifs CD4 CD8aa dans la persistance et la réactivation de la bactérie |
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| Interleukin 1/Toll-like receptor-induced autophosphorylation activates interleukin 1 receptor-associated kinase 4 and controls cytokine induction in a cell type-specific manner |
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| Interleukin-36-receptor antagonist deficiency and generalized pustular psoriasis |
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| INTERLEUKIN-7 RECEPTOR α CHAIN–DEPENDENT SIGNALING IS REQUIRED FOR T-CELL DEVELOPMENT |
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| IRAK-4- and MyD88-dependent pathways are essential for the removal of developing autoreactive B cells in humans |
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| IRAK-4 mutation (Q293X): rapid detection and characterization of defective post-transcriptional TLR/IL-1R responses in human myeloid and non-myeloid cells |
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| IRAK4 Deficiency in a Patient with Recurrent Pneumococcal Infections: Case Report and Review of the Literature |
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| Isolated congenital asplenia: a French nationwide retrospective survey of 20 cases |
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| Lessons learned from the study of human inborn errors of innate immunity |
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| Mechanism of dysfunction of human variants of the IRAK4 kinase and a role for its kinase activity in interleukin-1 receptor signaling |
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| Molecular mechanisms of mucocutaneous immunity against Candida and Staphylococcus species. |
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| Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies |
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| Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells |
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| The nature of human IL-6 |
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| Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance |
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| NEMO is a key component of NF-κB- and IRF-3-dependent TLR3-mediated immunity to herpes simplex virus. |
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| The NEMO mutation creating the most-upstream premature stop codon is hypomorphic because of a reinitiation of translation. |
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| New clinical phenotypes of fungal infections in special hosts |
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| New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO protein |
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| Un nouveau défaut héréditaire chez l'homme : déficit en TIRAP |
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| A novel form of cell type-specific partial IFN-gammaR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon |
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| A novel gain-of-function IKBA mutation underlies ectodermal dysplasia with immunodeficiency and polyendocrinopathy |
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| Nuclear factor kappaB essential modulator-deficient child with immunodeficiency yet without anhidrotic ectodermal dysplasia |
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| Posaconazole treatment of extensive skin and nail dermatophytosis due to autosomal recessive deficiency of CARD9. |
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| Primary immunodeficiencies associated with pneumococcal disease |
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| Primary immunodeficiencies underlying fungal infections |
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| Pyogenic bacterial infections in humans with MyD88 deficiency |
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| A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity |
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| Recurrent staphylococcal cellulitis and subcutaneous abscesses in a child with autoantibodies against IL-6. |
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| Régulation de la biologie des Lymphocytes T CD4+ conventionnels par les facteurs de transcription NF-κB |
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| Régulation des voies NF-KB au cours de la réponse immunitaire innée |
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| Regulation of NF-KB pathways during the innate immune response. |
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| Renal failure associated with APECED and terminal 4q deletion: evidence of autoimmune nephropathy |
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| Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency |
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| Rhinoscleroma: a French national retrospective study of epidemiological and clinical features |
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| Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia |
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| The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies |
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| The Role of Human IL-17 Immunity in Fungal Disease |
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| Role of immune responsiveness and DNA repair capacity genes in ageing |
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| Ruxolitinib Response in an Infant with Very-Early-Onset Inflammatory Bowel Disease and Gain-of-Function STAT1 Mutation |
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| Selective predisposition to bacterial infections in IRAK-4-deficient children: IRAK-4-dependent TLRs are otherwise redundant in protective immunity |
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| Self-reactive VH4-34-expressing IgG B cells recognize commensal bacteria |
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| Septicemia without sepsis: inherited disorders of nuclear factor-kappa B-mediated inflammation |
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| Simple diagnosis of STAT1 gain-of-function alleles in patients with chronic mucocutaneous candidiasis |
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| Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation |
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| Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey |
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| STAT1 Gain-of-Function and Dominant Negative STAT3 Mutations Impair IL-17 and IL-22 Immunity Associated with CMC. |
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| Successful Allogenic Stem Cell Transplantation in Patients with Inherited CARD9 Deficiency |
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| Susceptibilité génétique et infection chez l’enfant |
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| Systemic Human ILC Precursors Provide a Substrate for Tissue ILC Differentiation. |
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| Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature |
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| TLR3 deficiency in patients with herpes simplex encephalitis |
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| TLR8-mediated NF-κB and JNK Activation Are TAK1-independent and MEKK3-dependent |
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| The transmembrane activator TACI triggers immunoglobulin class switching by activating B cells through the adaptor MyD88 |
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| Tuberculosis and impaired IL-23-dependent IFN-γ immunity in humans homozygous for a common missense variant |
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| A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency |
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| Very late-onset group B Streptococcus meningitis, sepsis, and systemic shigellosis due to interleukin-1 receptor-associated kinase-4 deficiency. |
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| Whole-exome-sequencing-based discovery of human FADD deficiency |
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| WITHDRAWN: Genetic infectious susceptibility and TLR defects in human |
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| ZNF341 controls STAT3 expression and thereby immunocompetence |
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