About: Maria Grazia Roncarolo

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Italian pediatrician

Attributes	Values
rdf:type	Item
owl:sameAs	Maria Grazia Roncarolo
description	연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідниця (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtuese (sq) Italian pediatrician (en)
rdfs:label	Maria Grazia Roncarolo (en) Maria Grazia Roncarolo (es) Maria Grazia Roncarolo (it) Maria Grazia Roncarolo (nl) Maria Grazia Roncarolo (ast)
skos:prefLabel	Maria Grazia Roncarolo (en) Maria Grazia Roncarolo (es) Maria Grazia Roncarolo (it) Maria Grazia Roncarolo (nl) Maria Grazia Roncarolo (ast)
name	Maria Grazia Roncarolo (en) Maria Grazia Roncarolo (es) Maria Grazia Roncarolo (it) Maria Grazia Roncarolo (nl) Maria Grazia Roncarolo (ast)
Scopus author ID	wds:Q56426635-38D08007-98FC-4597-9E60-F895A6BB07B4
AE member ID	wds:Q56426635-AB10C128-6BAE-43BD-8B72-41DCC7BBE0F7
Scopus author ID	35453055700
AE member ID	Roncarolo_Maria
given name	wds:Q56426635-6E4A5F7B-C51D-4F64-BFF3-09340B9DBFD9
given name	Maria
instance of	wds:Q56426635-C7CBB496-B4FD-4D1D-BF7B-781CE277C47F
instance of	Homo sapiens
Google Knowledge Graph ID	wds:Q56426635-FF9D479A-C3F8-4A65-8E59-DA6444BFFFCC
Google Knowledge Graph ID	http://g.co/kg/g/11fj5d35yy
Google Knowledge Graph ID	/g/11fj5d35yy
ResearchGate profile ID	wds:Q56426635-92b39e72-4330-46b5-9dd8-956d2ec21837
ResearchGate profile ID	Maria_Grazia_Roncarolo
IRIS UNISR author ID	wds:Q56426635-1DB87341-81B8-44F8-A504-4A0A87276BF3
IRIS UNISR author ID	00079
skos:altLabel	Maria G. Roncarolo (en) Maria G. Roncarolo (es) Maria G. Roncarolo (nl) Maria G. Roncarolo (ast)
occupation	wds:Q56426635-8795541E-4BB7-4F1E-A27B-D78050E148A1
employer	wds:Q56426635-1CE7A5D1-653F-495D-98F0-9D7533983514
place of birth	wds:Q56426635-097E4295-1881-4285-A23B-76D52929F141
sex or gender	wds:Q56426635-1965AB61-EEA2-40FD-AFF9-074D1063C8CE
member of	wds:Q56426635-3B4CEF13-CE65-4D8B-BEA8-6CA6183E813F
date of birth	wds:Q56426635-e68b9007-3292-41ca-b1ac-1a555330d445
educated at	wds:Q56426635-AC6D6DD8-3943-47AD-9C04-B077ED281663
occupation	researcher
employer	Stanford University School of Medicine
place of birth	Turin
sex or gender	female organism
member of	Academia Europaea
date of birth	1954-01-01 00:00:00Z (xsd:dateTime)
educated at	University of Turin
ORCID iD	wds:Q56426635-c5338441-42cc-2cd6-f173-69c28a16dadd
is owl:sameAs of	Maria Grazia Roncarolo
is about of	Maria Grazia Roncarolo https://www.wikidata.org/wiki/Special:EntityData/Q56426635 Maria Grazia Roncarolo
is author of	Recombinant human interleukin 10 suppresses gliadin dependent T cell activation in ex vivo cultured coeliac intestinal mucosa. Interleukin-10-secreting type 1 regulatory T cells in rodents and humans. Point mutants of forkhead box P3 that cause immune dysregulation, polyendocrinopathy, enteropathy, X-linked have diverse abilities to reprogram T cells into regulatory T cells Activation of the aryl hydrocarbon receptor promotes allograft-specific tolerance through direct and dendritic cell-mediated effects on regulatory T cells Human IL2RA null mutation mediates immunodeficiency with lymphoproliferation and autoimmunity Health related quality of life in Middle Eastern children with beta-thalassemia Rapamycin selectively expands CD4+CD25+FoxP3+ regulatory T cells. Generation of potent and stable human CD4+ T regulatory cells by activation-independent expression of FOXP3. Differentiation of type 1 T regulatory cells (Tr1) by tolerogenic DC-10 requires the IL-10-dependent ILT4/HLA-G pathway Regulatory T-cell immunotherapy for tolerance to self antigens and alloantigens in humans. The cellular and molecular mechanisms of immuno-suppression by human type 1 regulatory T cells Identification of a common T/natural killer cell progenitor in human fetal thymus. Temporal, quantitative, and functional characteristics of single-KIR-positive alloreactive natural killer cell recovery account for impaired graft-versus-leukemia activity after haploidentical hematopoietic stem cell transplantation. Characterization of new arylsulfatase A gene mutations reinforces genotype-phenotype correlation in metachromatic leukodystrophy. Human cd25(+)cd4(+) t regulatory cells suppress naive and memory T cell proliferation and can be expanded in vitro without loss of function. Loss of mismatched HLA in leukemia after stem-cell transplantation. A hypomorphic R229Q Rag2 mouse mutant recapitulates human Omenn syndrome A CD4+ T-cell subset inhibits antigen-specific T-cell responses and prevents colitis Regulatory T cells: recommendations to simplify the nomenclature. Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome. Lentiviral hematopoietic stem cell gene therapy benefits metachromatic leukodystrophy Recent advances in understanding the pathophysiology of Wiskott-Aldrich syndrome Multilineage hematopoietic reconstitution without clonal selection in ADA-SCID patients treated with stem cell gene therapy Gene therapy for immunodeficiency due to adenosine deaminase deficiency. The role of IL-10 and TGF-beta in the differentiation and effector function of T regulatory cells Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning IL-10 and TGF-beta induce alloreactive CD4+CD25- T cells to acquire regulatory cell function Rapamycin monotherapy in patients with type 1 diabetes modifies CD4+CD25+FOXP3+ regulatory T-cells Differentiation of Tr1 cells by immature dendritic cells requires IL-10 but not CD25+CD4+ Tr cells Wiskott-Aldrich syndrome protein regulates lipid raft dynamics during immunological synapse formation. Gene therapy for adenosine deaminase deficiency Hepatocyte-targeted expression by integrase-defective lentiviral vectors induces antigen-specific tolerance in mice with low genotoxic risk In vivo tracking of T cells in humans unveils decade-long survival and activity of genetically modified T memory stem cells

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