About: Marie-José Stasia

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Stasia, Marie-José (1959-.... ; auteure en biologie) Stasia, Marie-José (1959-.... ; auteure en biologie) Stasia, Marie-José (1959-.... ; auteure en biologie) Stasia, Marie-José (1959-.... ; auteure en biologie)
alternative label	Pauger, Marie-José Stasia Stasia Pauger, Marie-José
Life Event	http://www.idref.fr/068665652/birth
preferred label	Stasia, Marie-José (1959-.... ; auteure en biologie)
name	Marie-José Stasia
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
isni:identifierValid	000000035766269X
Given name	Marie-José
familyName	Stasia
note	Auteure d'une thèse d'exercice en pharmacie (Grenoble 1, 1982), d'une thèse d'université en pharmacie (Grenoble 1, 1984) et d'une thèse de doctorat en biologie (Grenoble 1, 1990). - Directrice de thèse à l'Université Joseph Fourier de Grenoble, en poste au laboratoire TIMC-IMAG (en 2009)
gender	female
ORCID iD	0000-0003-4466-4880
ISI Researcher ID	M-7165-2014
Scopus ID	6701661130
is sameAs of	Stasia, Marie-José (1959-.... ; auteure en biologie) Stasia, Marie-José (1959-.... ; auteure en biologie) Stasia, Marie-José (1959-.... ; auteure en biologie) Stasia, Marie-José (1959-.... ; auteure en biologie)
is Thesis advisor of	La bactéricidie des neutrophiles, mécanismes cellulaires et moléculaires et leurs dysfonctions Dysfonctionnement de la NADPH oxydase des phagocytes dans la granulomatose septique chronique de type X+, Modèle d'étude : les cellules PLB-985 CGD X http://www.sudoc.fr/202968731/id http://www.sudoc.fr/138508895/id http://www.sudoc.fr/17251679X/id Mise en place d'un modèle cellulaire d'étude des granulomatoses septiques chroniques autosomales récessives http://www.sudoc.fr/06866365X/id Régulation de l'activité NADPH oxydase phagocytaire, mécanismes moléculaires de la super-activité oxydase du cytochrome b558 D-loopNox4-Nox2 http://www.sudoc.fr/198442785/id http://www.sudoc.fr/095868372/id http://www.sudoc.fr/14485337X/id http://www.sudoc.fr/06679580X/id http://www.sudoc.fr/081668023/id http://www.sudoc.fr/247132039/id http://www.sudoc.fr/246864575/id http://www.sudoc.fr/20366521X/id http://www.sudoc.fr/247176400/id http://www.sudoc.fr/274149427/id http://www.sudoc.fr/274130386/id La granulomatose septique chronique, approche biotechnologique de thérapie cellulaire ex vivo, mise en place de modèles d'étude La granulomatose septique chronique, synthèse et étude des formes variantes http://www.sudoc.fr/283729740/id
is Author of	http://www.sudoc.fr/042215471/id http://www.sudoc.fr/008858942/id http://www.sudoc.fr/113100833/id Regulation of NADPH oxidase activity in phagocytes: relationship between FAD/NADPH binding and oxidase complex assembly. Differential impact of glucose levels and advanced glycation end-products on tubular cell viability and pro-inflammatory/profibrotic functions Second Report of Chronic Granulomatous Disease in Jordan: Clinical and Genetic Description of 31 Patients From 21 Different Families, Including Families From Lybia and Iraq http://www.sudoc.fr/245490396/id Functional and genetic characterization of two extremely rare cases of Williams-Beuren syndrome associated with chronic granulomatous disease. https://archive-ouverte.unige.ch/unige:82438#id Rare duplication or deletion of exons 6, 7 and 8 in CYBB leading to X-linked chronic granulomatous disease in two patients from different families. NOX4 is the main NADPH oxidase involved in the early stages of hematopoietic differentiation from human induced pluripotent stem cells Characterization of six novel mutations in the CYBB gene leading to different sub-types of X-linked chronic granulomatous disease. First report of clinical, functional, and molecular investigation of chronic granulomatous disease in nine Jordanian families. Potent inhibition of store-operated Ca2+ influx and superoxide production in HL60 cells and polymorphonuclear neutrophils by the pyrazole derivative BTP2. Poikiloderma with neutropenia, Clericuzio type, in a family from Morocco. MC1R expression in HaCaT keratinocytes inhibits UVA-induced ROS production via NADPH oxidase- and cAMP-dependent mechanisms. The 23-kilodalton protein, a substrate of protein kinase C in bovine neutrophil cytosol is a member of the S100 family Optimized Generation of Functional Neutrophils and Macrophages from Patient-Specific Induced Pluripotent Stem Cells: Ex Vivo Models of X 0 -Linked, AR22 0 - and AR47 0 - Chronic Granulomatous Diseases Syndrome d’activation lymphohistiocytaire associé à une infection à Burkholderia cepacia complex chez un nourrisson révélant une granulomatose septique et une intégration génomique du virus HHV-6 [Lymphohistiocytic activation syndrome and Burkholderia cepacia complex infection in a child revealing chronic granulomatous disease and chromosomal integration of the HHV-6 genome]. https://archive-ouverte.unige.ch/unige:162638#id Purification and characterization of an isoform of protein kinase C from bovine neutrophils Towards routine screening of rare genetic diseases: the example of chronic granulomatous disease. Severe Clinical Forms of Cytochrome b-Negative Chronic Granulomatous Disease (X91−) in 3 Brothers with a Point Mutation in the Promoter Region of CYBB Characterization of superoxide overproduction by the D-Loop(Nox4)-Nox2 cytochrome b(558) in phagocytes-Differential sensitivity to calcium and phosphorylation events. CRISPR-gene-engineered CYBB knock-out PLB-985 cells, a useful model to study functional impact of X-linked chronic granulomatous disease mutations: application to the G412E X91+-CGD mutation Caractérisation et propriétés respiratoires des phagolysosomes de polymorphonucléaires neutrophiles de bovins Role of putative second transmembrane region of Nox2 protein in the structural stability and electron transfer of the phagocytic NADPH oxidase. Clinical, functional and genetic characterization of 16 patients suffering from chronic granulomatous disease variants – identification of 11 novel mutations in CYBB Clinical, functional and genetic analysis of twenty-four patients with chronic granulomatous disease - identification of eight novel mutations in CYBB and NCF2 genes. Altered Humoral Immune Responses and IgG Subtypes in NOX2-Deficient Mice and Patients: A Key Role for NOX2 in Antigen-Presenting Cells New insights into the membrane topology of the phagocyte NADPH oxidase: characterization of an anti-gp91-phox conformational monoclonal antibody. Three common polymorphisms in the CYBA gene form a haplotype associated with decreased ROS generation. Resistant Invasive Aspergillosis in an Autosomal Recessive Chronic Granulomatous Disease. Crucial role of two potential cytosolic regions of Nox2, 191TSSTKTIRRS200 and 484DESQANHFAVHHDEEKD500, on NADPH oxidase activation. A novel point mutation in the CYBB gene promoter leading to a rare X minus chronic granulomatous disease variant - impact on the microbicidal activity of neutrophils. Scavenging of reactive oxygen species by tryptophan metabolites helps Pseudomonas aeruginosa escape neutrophil killing. Characterization of NADPH Oxidase Expression and Activity in Acute Myeloid Leukemia Cell Lines: A Correlation with the Differentiation Status Purification, caractérisation de la protéine kinase C du neutrophile bovin et mise en évidence d'un substrat potentiel ayant les caractéristiques d'une protéine G de petite taille Copurification of rho protein and the rho-GDP dissociation inhibitor from bovine neutrophil cytosol. Effect of phosphoinositides on rho ADP-ribosylation by the C3 exoenzyme of Clostridium botulinum Genetics and immunopathology of chronic granulomatous disease. Identification of NOX2 regions for normal biosynthesis of cytochrome b558 in phagocytes highlighting essential residues for p22phox binding [Chronic-granulomatous disease] http://www.sudoc.fr/274141507/id European contribution to the study of ROS: A summary of the findings and prospects for the future from the COST action BM1203 (EU-ROS) Genetic diagnosis of primary immunodeficiencies: A survey of the French national registry A 23-kDa protein as a substrate for protein kinase C in bovine neutrophils. Purification and partial characterization Leu505 of Nox2 is crucial for optimal p67phox-dependent activation of the flavocytochrome b558 during phagocytic NADPH oxidase assembly. Optimization of X-linked chronic granulomatous disease modelization by using patient-specific induced pluripotent stem cells RAGE and CYBA polymorphisms are associated with microalbuminuria and end-stage renal disease onset in a cohort of type 1 diabetes mellitus patients over a 20-year follow-up A novel point mutation in the gene promoter leading to a rare X minus chronic granulomatous disease variant – Impact on the microbicidal activity of neutrophils Therapeutic effects of proteoliposomes on X-linked chronic granulomatous disease: proof of concept using macrophages differentiated from patient-specific induced pluripotent stem cells Hematologically important mutations: X-linked chronic granulomatous disease (third update). The X-CGD PLB-985 Cell Model for NOX2 Structure-Function Analysis https://archive-ouverte.unige.ch/unige:5421#id

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