About: Jordan Orange

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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
field of work	wds:Q42881963-6C28119A-10BA-4349-8192-60FD556F09C1 wds:Q42881963-F3D14459-F7FB-4AF8-953B-954C274EC374
field of work	pediatrics immunology
description	forskare (sv) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Jordan Orange (en) Jordan Orange (es) Jordan Orange (nl) Jordan Orange (sl) Jordan Orange (ast)
skos:prefLabel	Jordan Orange (en) Jordan Orange (es) Jordan Orange (nl) Jordan Orange (sl) Jordan Orange (ast)
name	Jordan Orange (en) Jordan Orange (es) Jordan Orange (nl) Jordan Orange (sl) Jordan Orange (ast)
Scopus author ID	wds:Q42881963-FAB0A879-1BCD-4370-8EA1-178C1C167753
Scopus author ID	7004197590
given name	wds:Q42881963-6E527E8E-A3BC-49BC-A621-77DDBC7C4B06
given name	Jordan
instance of	wds:Q42881963-75DE3764-196C-47D3-B7CB-262FFDB00C05
instance of	Homo sapiens
award received	wds:Q42881963-12E4321D-EFEC-43D5-B639-9E85FD9031FF
award received	Fellow of the New York Academy of Medicine
occupation	wds:Q42881963-636FC89A-A2AA-4E5F-B6FA-754BDB4750B7
sex or gender	wds:Q42881963-C26E43B6-758F-47CB-B4FB-AA9625F63FE9
VIAF ID	wds:Q42881963-4EF08902-99EB-411E-BDE0-C59E2253CF2F
GND ID	wds:Q42881963-56765410-898c-4d46-954c-d5f6f22a8b00
Library of Congress authority ID	wds:Q42881963-C420301B-1FD1-45D9-8EDF-E25E451F2358
openMLOL author ID	wds:Q42881963-ED6B1522-644A-47CB-9440-5343D1973078
member of	wds:Q42881963-64CAD5A5-8623-41BA-BC91-01155AC5AF09
academic degree	wds:Q42881963-52F98BB8-D132-4358-8652-A8B4BA906F47 wds:Q42881963-B0920227-D2E9-4D6B-812F-06D20DD21A05
family name	wds:Q42881963-2F85D29C-DED2-413D-8615-3D8B1EF49DCD
WorldCat Identities ID (superseded)	wds:Q42881963-7564BAB8-99F6-43CB-8392-76BF8CEAECCC
National Library of Israel J9U ID	wds:Q42881963-010CEC4D-6437-4806-9C16-8140AF0C9FB3
VIAF ID	http://viaf.org/viaf/9378734
GND ID	https://d-nb.info/gnd/137174837
Library of Congress authority ID	http://id.loc.gov/authorities/names/nb2008011863
occupation	researcher
sex or gender	male
VIAF ID	9378734
GND ID	137174837
Library of Congress authority ID	nb2008011863
openMLOL author ID	299031
member of	New York Academy of Medicine
academic degree	Doctor of Philosophy Doctor of Medicine
family name	Orange
WorldCat Identities ID (superseded)	lccn-nb2008011863
National Library of Israel J9U ID	987007371322805171
ORCID iD	wds:Q42881963-8700F33D-3AE8-47EB-B6BF-9496D7FFA361
ORCID iD	https://orcid.org/0000-0001-7117-7725
ORCID iD	0000-0001-7117-7725
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42881963
is author of	Natural killer cells inhibit hepatitis C virus expression Interferon-alpha/beta inhibition of interleukin 12 and interferon-gamma production in vitro and endogenously during viral infection Mechanism of interleukin 12-mediated toxicities during experimental viral infections: role of tumor necrosis factor and glucocorticoids Wiskott-Aldrich syndrome protein is required for NK cell cytotoxicity and colocalizes with actin to NK cell-activating immunologic synapses Formation of a WIP-, WASp-, actin-, and myosin IIA-containing multiprotein complex in activated NK cells and its alteration by KIR inhibitory signaling Variants of DENND1B associated with asthma in children Asymmetric T lymphocyte division in the initiation of adaptive immune responses. Compound heterozygous CORO1A mutations in siblings with a mucocutaneous-immunodeficiency syndrome of epidermodysplasia verruciformis-HPV, molluscum contagiosum and granulomatous tuberculoid leprosy Novel inborn error of folate metabolism: identification by exome capture and sequencing of mutations in the MTHFD1 gene in a single proband Severe combined immunodeficiency resulting from mutations in MTHFD1. GATA2 deficiency: a protean disorder of hematopoiesis, lymphatics, and immunity. Interleukin-1-induced NF-kappaB activation is NEMO-dependent but does not require IKKbeta The adaptor molecule SAP plays essential roles during invariant NKT cell cytotoxicity and lytic synapse formation Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome. Human immunodeficiency-causing mutation defines CD16 in spontaneous NK cell cytotoxicity Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56(bright) subset. Natural killer cell deficiency Finding NEMO: genetic disorders of NF-κB activation Eosinophilic fasciitis mimicking angioedema and treatment response to infliximab in a pediatric patient Human natural killer cell deficiencies Human natural killer cell deficiencies and susceptibility to infection miR-451 protects against erythroid oxidant stress by repressing 14-3-3zeta Disseminated varicella infection due to the vaccine strain of varicella-zoster virus, in a patient with a novel deficiency in natural killer T cells A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene Intravenous immunoglobulins. Current understanding and future directions. The mature activating natural killer cell immunologic synapse is formed in distinct stages

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