Anne Puel chercheuse
Puel, Anne
VIAF ID: 304446186 (Personal)
Permalink: http://viaf.org/viaf/304446186
Preferred Forms
- 100 0 _ ‡a Anne Puel ‡c chercheuse
- 100 1 _ ‡a PUEL, ANNE.
- 100 1 _ ‡a Puel, Anne
- 100 1 _ ‡a 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 | |
A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency | |
Identification et caractérisation des bases génétiques moléculaires responsables de la prédisposition à la candidose cutanéo-muqueuse chronique chez l'homme | |
IgM+IgD+CD27+ B cells are markedly reduced in IRAK-4-, MyD88-, and TIRAP- but not UNC-93B-deficient patients | |
Immunity to infection in IL-17-deficient mice and humans | |
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 | |
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19 | |
Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated exons | |
Infections fongiques invasives et déficit en CARD9. | |
Infectious diseases in patients with IRAK-4, MyD88, NEMO, or IκBα deficiency | |
Inherited CARD9 Deficiency in a Patient with Both Exophiala spinifera and Aspergillus nomius Severe Infections | |
Inherited CARD9 deficiency in otherwise healthy children and adults with Candida species-induced meningoencephalitis, colitis, or both | |
Inherited disorders of human Toll-like receptor signaling: immunological implications. | |
Inherited human IRAK-4 deficiency: an update. | |
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 | |
Interleukin 1/Toll-like receptor-induced autophosphorylation activates interleukin 1 receptor-associated kinase 4 and controls cytokine induction in a cell type-specific manner | |
Interleukin-36-receptor antagonist deficiency and generalized pustular psoriasis | |
INTERLEUKIN-7 RECEPTOR α CHAIN–DEPENDENT SIGNALING IS REQUIRED FOR T-CELL DEVELOPMENT | |
IRAK-4- and MyD88-dependent pathways are essential for the removal of developing autoreactive B cells in humans | |
IRAK-4 mutation (Q293X): rapid detection and characterization of defective post-transcriptional TLR/IL-1R responses in human myeloid and non-myeloid cells | |
IRAK4 Deficiency in a Patient with Recurrent Pneumococcal Infections: Case Report and Review of the Literature | |
Isolated congenital asplenia: a French nationwide retrospective survey of 20 cases | |
Lessons learned from the study of human inborn errors of innate immunity | |
Mechanism of dysfunction of human variants of the IRAK4 kinase and a role for its kinase activity in interleukin-1 receptor signaling | |
A mild form of SLC29A3 disorder: a frameshift deletion leads to the paradoxical translation of an otherwise noncoding mRNA splice variant | |
Molecular mechanisms of mucocutaneous immunity against Candida and Staphylococcus species. | |
Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies | |
Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells | |
The nature of human IL-6 | |
Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance | |
NEMO is a key component of NF-κB- and IRF-3-dependent TLR3-mediated immunity to herpes simplex virus. | |
The NEMO mutation creating the most-upstream premature stop codon is hypomorphic because of a reinitiation of translation. | |
New clinical phenotypes of fungal infections in special hosts | |
New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO protein | |
Un nouveau défaut héréditaire chez l'homme : déficit en TIRAP | |
A novel form of cell type-specific partial IFN-gammaR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon | |
A novel gain-of-function IKBA mutation underlies ectodermal dysplasia with immunodeficiency and polyendocrinopathy | |
Nuclear factor kappaB essential modulator-deficient child with immunodeficiency yet without anhidrotic ectodermal dysplasia | |
Posaconazole treatment of extensive skin and nail dermatophytosis due to autosomal recessive deficiency of CARD9. | |
Primary immunodeficiencies associated with pneumococcal disease | |
Primary immunodeficiencies underlying fungal infections | |
Pyogenic bacterial infections in humans with MyD88 deficiency | |
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity | |
Recurrent staphylococcal cellulitis and subcutaneous abscesses in a child with autoantibodies against IL-6. | |
Régulation de la biologie des Lymphocytes T CD4+ conventionnels par les facteurs de transcription NF-κB | |
Régulation des voies NF-KB au cours de la réponse immunitaire innée | |
Regulation of NF-KB pathways during the innate immune response. | |
Renal failure associated with APECED and terminal 4q deletion: evidence of autoimmune nephropathy | |
Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency | |
Rhinoscleroma: a French national retrospective study of epidemiological and clinical features | |
Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia | |
The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies | |
The Role of Human IL-17 Immunity in Fungal Disease | |
Role of immune responsiveness and DNA repair capacity genes in ageing | |
Ruxolitinib Response in an Infant with Very-Early-Onset Inflammatory Bowel Disease and Gain-of-Function STAT1 Mutation | |
Selective predisposition to bacterial infections in IRAK-4-deficient children: IRAK-4-dependent TLRs are otherwise redundant in protective immunity | |
Self-reactive VH4-34-expressing IgG B cells recognize commensal bacteria | |
Septicemia without sepsis: inherited disorders of nuclear factor-kappa B-mediated inflammation | |
Simple diagnosis of STAT1 gain-of-function alleles in patients with chronic mucocutaneous candidiasis | |
Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation | |
Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey | |
STAT1 Gain-of-Function and Dominant Negative STAT3 Mutations Impair IL-17 and IL-22 Immunity Associated with CMC. | |
Successful Allogenic Stem Cell Transplantation in Patients with Inherited CARD9 Deficiency | |
Susceptibilité génétique et infection chez l’enfant | |
Systemic Human ILC Precursors Provide a Substrate for Tissue ILC Differentiation. | |
Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature | |
TLR3 deficiency in patients with herpes simplex encephalitis | |
TLR8-mediated NF-κB and JNK Activation Are TAK1-independent and MEKK3-dependent | |
The transmembrane activator TACI triggers immunoglobulin class switching by activating B cells through the adaptor MyD88 | |
Tuberculosis and impaired IL-23-dependent IFN-γ immunity in humans homozygous for a common missense variant | |
A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency | |
Very late-onset group B Streptococcus meningitis, sepsis, and systemic shigellosis due to interleukin-1 receptor-associated kinase-4 deficiency. | |
Whole-exome-sequencing-based discovery of human FADD deficiency | |
WITHDRAWN: Genetic infectious susceptibility and TLR defects in human | |
ZNF341 controls STAT3 expression and thereby immunocompetence |