About: Jacinta Bustamante

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

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) investigadora (es) ഗവേഷക (ml) araştırmacı (tr) дослідниця (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) onderzoeker (nl) researcher (en-ca) researcher (en-gb) researcher (en-us) hulumtuese (sq) ricercatrice (it) investigadora (ca) investigadora (gl) investigadora (pt) investigadora (ast) Médecin Chercheur (fr)
rdfs:label	Jacinta Bustamante (en) Jacinta Bustamante (es) Jacinta Bustamante (fr) Jacinta Bustamante (nl) Jacinta Bustamante (sl) Jacinta Bustamante (ast)
skos:prefLabel	Jacinta Bustamante (en) Jacinta Bustamante (es) Jacinta Bustamante (fr) Jacinta Bustamante (nl) Jacinta Bustamante (sl) Jacinta Bustamante (ast)
name	Jacinta Bustamante (en) Jacinta Bustamante (es) Jacinta Bustamante (fr) Jacinta Bustamante (nl) Jacinta Bustamante (sl) Jacinta Bustamante (ast)
given name	wds:Q41112850-2FA8C05E-5E27-4E94-826F-C93F925E7476
given name	Jacinta
instance of	wds:Q41112850-6BEC9308-7E1D-4C89-8E6B-9156EE7A1BB7
instance of	Homo sapiens
doctoral advisor	wds:Q41112850-2f30105a-e8b5-4b83-8201-4977302323e5
doctoral advisor	Jean-Laurent Casanova
occupation	wds:Q41112850-7362A303-4B7B-4892-9C8E-629DD8B2E621
sex or gender	wds:Q41112850-5089A6CC-5158-4EFE-8247-72EFCDD0F3F4
VIAF ID	wds:Q41112850-2ED2F52D-24C2-40A6-B0FC-BA4797E0690C
IdRef ID	wds:Q41112850-A9D509ED-517F-40B3-9D63-1F8465527EAB
date of birth	wds:Q41112850-292C7246-358D-4849-A004-9D2F5E34DF5F
PLWABN ID	wds:Q41112850-3E2E55CC-32C6-4002-9C35-E5BAF05E9976
family name	wds:Q41112850-9966716C-1A82-4DEC-AE92-4C80A20B0CD8
WorldCat Identities ID (superseded)	wds:Q41112850-72BB6EE5-0430-4C95-9316-0B9C4C6AB97A
VIAF ID	http://viaf.org/viaf/198899649
IdRef ID	http://www.idref.fr/124593461/id
occupation	researcher
sex or gender	female organism
VIAF ID	198899649
IdRef ID	124593461
date of birth	1968-01-01 00:00:00Z (xsd:dateTime)
PLWABN ID	9810692768305606
family name	Bustamante
WorldCat Identities ID (superseded)	viaf-198899649
ORCID iD	wds:Q41112850-25E5E515-5F4D-4A04-B021-A949F2F48978
ORCID iD	https://orcid.org/0000-0002-3439-2482
ORCID iD	0000-0002-3439-2482
ResearcherID	wds:Q41112850-9C154D52-750C-4806-8C60-F83A129E17A2
Publons author ID	wds:Q41112850-307c12a8-8072-45c5-9e62-963f8a512a15
ResearcherID	H-7877-2017
Publons author ID	2109833
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q41112850
is author of	IRF8 mutations and human dendritic-cell immunodeficiency Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiency Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation Novel primary immunodeficiencies revealed by the investigation of paediatric infectious diseases X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production Pyogenic bacterial infections in humans with IRAK-4 deficiency B cell-intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I Inborn errors of IL-12/23- and IFN-gamma-mediated immunity: molecular, cellular, and clinical features IL-12Rβ1 deficiency: mutation update and description of the IL12RB1 variation database IL-12Rβ1 deficiency in two of fifty children with severe tuberculosis from Iran, Morocco, and Turkey Clinical disease caused by Klebsiella in 2 unrelated patients with interleukin 12 receptor beta1 deficiency Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta1 deficiency: medical and immunological implications Haploinsufficiency at the human IFNGR2 locus contributes to mycobacterial disease Inherited IL-12p40 deficiency: genetic, immunologic, and clinical features of 49 patients from 30 kindreds Lethal tuberculosis in a previously healthy adult with IL-12 receptor deficiency A novel form of complete IL-12/IL-23 receptor beta1 deficiency with cell surface-expressed nonfunctional receptors. 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 Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries Accounting for genetic heterogeneity in homozygosity mapping: application to Mendelian susceptibility to mycobacterial disease New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO protein Primary immunodeficiencies associated with pneumococcal disease Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update)

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