Emmanuelle Jouanguy chercheuse
Jouanguy, Emmanuelle
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
VIAF ID: 127152079229707112896 (Personal)
Permalink: http://viaf.org/viaf/127152079229707112896
Preferred Forms
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100 0 _
‡a
Emmanuelle Jouanguy
‡c
chercheuse
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100 1 _
‡a
Jouanguy, Emmanuelle
4xx's: Alternate Name Forms (4)
Works
| Title | Sources |
|---|---|
| DEFAUTS HEREDITAIRES DU RECEPTEUR DE L'INTERFERON GAMMA CHEZ L'HOMME |
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| Familial NK cell deficiency associated with impaired IL-2- and IL-15-dependent survival of lymphocytes. |
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| Fatal Cytomegalovirus Infection in an Adult with Inherited NOS2 Deficiency |
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| Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis |
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| Genetic and molecular definition of complementation group D in MHC class II deficiency |
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| Homozygous NLRP1 gain-of-function mutation in siblings with a syndromic form of recurrent respiratory papillomatosis |
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| HPV-Related Skin Phenotypes in Patients with Inborn Errors of Immunity |
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| The human CIB1-EVER1-EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses |
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| Human complete Stat-1 deficiency is associated with defective type I and II IFN responses in vitro but immunity to some low virulence viruses in vivo |
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| Human genetic and immunological determinants of critical COVID-19 pneumonia |
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| Human inborn errors of immunity to infection affecting cells other than leukocytes: from the immune system to the whole organism |
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| Human interferon-gamma-mediated immunity is a genetically controlled continuous trait that determines the outcome of mycobacterial invasion |
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| Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation |
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| Human primary immunodeficiencies of type I interferons |
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| Human Toll-like receptor-dependent induction of interferons in protective immunity to viruses |
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| IAO03 Genetic susceptibility to herpes encephalitis in children |
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| Identification of an Endoglin Variant Associated With HCV-Related Liver Fibrosis Progression by Next-Generation Sequencing |
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| Idiopathic disseminated bacillus Calmette-Guérin infection: a French national retrospective study |
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| IFN-gamma and IL-12 differentially regulate CC-chemokine secretion and CCR5 expression in human T lymphocytes |
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| Immunological conditions of children with BCG disseminated infection |
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| The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants |
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| Impaired intrinsic immunity to HSV-1 in human iPSC-derived TLR3-deficient CNS cells |
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| Impaired response to interferon-alpha/beta and lethal viral disease in human STAT1 deficiency |
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| Impairment of mycobacterial immunity in human interleukin-12 receptor deficiency |
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| In a novel form of IFN-gamma receptor 1 deficiency, cell surface receptors fail to bind IFN-gamma |
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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 the development of human natural killer cells |
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| Infections in IFNGR-1-deficient children |
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| Inheritable defects in interleukin-12- and interferon-gamma-mediated immunity and the TH1/TH2 paradigm in man. |
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| Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency |
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| Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines |
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| Inherited IL-18BP deficiency in human fulminant viral hepatitis. |
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| Inherited Interleukin 2-Inducible T-Cell (ITK) Kinase Deficiency in Siblings With Epidermodysplasia Verruciformis and Hodgkin Lymphoma |
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| Inherited MST1 deficiency underlies susceptibility to EV-HPV infections |
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| Interferon gamma receptor 2 gene variants are associated with liver fibrosis in patients with chronic hepatitis C infection |
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| Interferon-gamma receptor deficiency: relationship between genotype, environment, and phenotype (Review) |
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| Interferon-γ receptor deficiency mimicking Langerhans’ cell histiocytosis |
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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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| JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency |
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| The Jak-STAT signaling pathway is required but not sufficient for the antiviral response of drosophila |
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| Kaposi Sarcoma of Childhood: Inborn or Acquired Immunodeficiency to Oncogenic HHV-8 |
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| Life-Threatening COVID-19: Defective Interferons Unleash Excessive Inflammation |
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| Life-Threatening Infections Due to Live-Attenuated Vaccines: Early Manifestations of Inborn Errors of Immunity |
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| LPS-induced immune response in Drosophila |
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| Mendelian susceptibility to mycobacterial infection in man |
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| Monoclonal antibody-mediated neutralization of SARS-CoV-2 in an IRF9-deficient child |
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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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| Nonpathogenic Common Variants of IFNGR1 and IFNGR2 in Association with Total Serum IgE Levels |
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| Novel primary immunodeficiencies revealed by the investigation of paediatric infectious diseases |
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| A novel primary immunodeficiency with specific natural-killer cell deficiency maps to the centromeric region of chromosome 8. |
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| Novel STAT1 alleles in otherwise healthy patients with mycobacterial disease |
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| Osteopontin expression correlates with clinical outcome in patients with mycobacterial infection. |
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| A partial form of recessive STAT1 deficiency in humans |
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| Partial interferon-gamma receptor 1 deficiency in a child with tuberculoid bacillus Calmette-Guérin infection and a sibling with clinical tuberculosis |
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| Partial MCM4 deficiency in patients with growth retardation, adrenal insufficiency, and natural killer cell deficiency |
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| Pherokine-2 and -3. |
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| Prédisposition génétique aux infections virales sévères. |
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| [Primary immunodeficiency secondary to ZAP-70 deficiency] |
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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 |
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| Recurrent elevated liver transaminases and acute liver failure in two siblings with novel bi-allelic mutations of NBAS. |
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| Recurrent staphylococcal cellulitis and subcutaneous abscesses in a child with autoantibodies against IL-6. |
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| RecurrentMycobacterium aviumOsteomyelitis Associated With a Novel Dominant Interferon Gamma Receptor Mutation |
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| Requirement for both IL-12 and IFN-gamma signaling pathways in optimal IFN-gamma production by human T cells |
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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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| RLTPR deficiency : a new genetic etiology of combined immunodeficiency |
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| A role for interleukin-12/23 in the maturation of human natural killer and CD56+ T cells in vivo |
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| SARS-CoV-2 induces human plasmacytoid predendritic cell diversification via UNC93B and IRAK4 |
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| Surface expression of the IFN-gamma R2 chain is regulated by intracellular trafficking in human T lymphocytes |
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| TIM3+ TRBV11-2 T cells and IFNγ signature in patrolling monocytes and CD16+ NK cells delineate MIS-C |
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| TLR3 controls constitutive IFN-β antiviral immunity in human fibroblasts and cortical neurons |
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| TLR3 deficiency in patients with herpes simplex encephalitis |
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| Toll-related receptors and the control of antimicrobial peptide expression in Drosophila |
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| A virus finds its natural killer |
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| Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma |
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| Whole-transcriptome sequencing-based concomitant detection of viral and human genetic determinants of cutaneous lesions |
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| WITHDRAWN: Genetic infectious susceptibility and TLR defects in human |
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