Ariane Chapgier
Chapgier, Ariane, 1979-....
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
VIAF ID: 198877091 (Personal)
Permalink: http://viaf.org/viaf/198877091
Preferred Forms
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100 0 _
‡a
Ariane Chapgier
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100 1 _
‡a
Chapgier, Ariane,
‡d
1979-
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100 1 _
‡a
Chapgier, Ariane,
‡d
1979-....
4xx's: Alternate Name Forms (2)
Works
| Title | Sources |
|---|---|
| Autosomal-dominant primary immunodeficiencies |
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| Bacillus Calmette Guérin triggers the IL-12/IFN-γ axis by an IRAK-4- and NEMO-dependent, non-cognate interaction between monocytes, NK, and T lymphocytes |
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| BCG-osis and tuberculosis in a child with chronic granulomatous disease |
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| The clinical spectrum of patients with deficiency of Signal Transducer and Activator of Transcription-1. |
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| Corrigendum to “Inborn errors of IL-12/23- and IFN-γ-mediated immunity: Molecular, cellular, and clinical features” [Semin. Immunol. 18 (2006) 347–361] |
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| Déficiences associées au gène STAT 1 chez l'homme. |
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| Distinct factors control histone variant H3.3 localization at specific genomic regions |
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| Gains of glycosylation mutations |
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| Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease |
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| Haploinsufficiency at the human IFNGR2 locus contributes to mycobacterial disease |
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| Hira-dependent histone H3.3 deposition facilitates PRC2 recruitment at developmental loci in ES cells |
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| HIRA directly targets the enhancers of selected cardiac transcription factors during in vitro differentiation of mouse embryonic stem cells |
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| HIRA Is Required for Heart Development and Directly Regulates Tnni2 and Tnnt3 |
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| Human STAT1 deficiencies |
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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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| Infection multifocale à Mycobacterium intracellulare: premier cas de déficit partiel dominant du récepteur de l'interféron gamma en milieu tropical français |
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| Infections Due to Various Atypical Mycobacteria in a Norwegian Multiplex Family with Dominant Interferon- Receptor Deficiency |
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| Inherited disorders of the IL-12-IFN-gamma axis in patients with disseminated BCG infection |
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| The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes |
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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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| Novel STAT1 alleles in otherwise healthy patients with mycobacterial disease |
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| A novel X-linked recessive form of Mendelian susceptibility to mycobaterial disease |
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| Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds |
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| Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN-gamma receptor 1 deficiency |
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| Prédisposition génétique et infections de l'enfant |
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| Successful hematopoietic stem cell transplantation in a child with active disseminated Mycobacterium fortuitum infection and interferon-γ receptor 1 deficiency |
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| T cell-dependent activation of dendritic cells requires IL-12 and IFN-gamma signaling in T cells |
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| TLR3 deficiency in patients with herpes simplex encephalitis |
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| X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production |
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