About: Rachel Wevrick

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

Canadian geneticist

Attributes	Values
rdf:type	Item
description	باحت (ary) Canada karimma ŋun nyɛ paɣa (dag) Canadian geneticist (en-ca) Canadian geneticist (en-gb) genetista canadiense (es) Canadian geneticist (en) عالمة وراثة كندية (ar) Canadees geneticus (nl) kanadische Professorin und Genetikerin (de)
rdfs:label	Rachel Wevrick (ca) Rachel Wevrick (en) Rachel Wevrick (es) Rachel Wevrick (fr) Rachel Wevrick (ga) Rachel Wevrick (it) Rachel Wevrick (nl) Rachel Wevrick (sl) Rachel Wevrick (sq) Rachel Wevrick (ast)
skos:prefLabel	Rachel Wevrick (ca) Rachel Wevrick (en) Rachel Wevrick (es) Rachel Wevrick (fr) Rachel Wevrick (ga) Rachel Wevrick (it) Rachel Wevrick (nl) Rachel Wevrick (sl) Rachel Wevrick (sq) Rachel Wevrick (ast)
name	Rachel Wevrick (ca) Rachel Wevrick (en) Rachel Wevrick (es) Rachel Wevrick (fr) Rachel Wevrick (ga) Rachel Wevrick (it) Rachel Wevrick (nl) Rachel Wevrick (sl) Rachel Wevrick (sq) Rachel Wevrick (ast)
Scopus author ID	wds:Q46130607-1854E15D-CF27-42E1-B712-EE4C9C3251AF
Scopus author ID	7003678821
given name	wds:Q46130607-3771a116-4bd1-bc96-cd38-531928c42a3d
given name	Rachel
instance of	wds:Q46130607-F8D76B54-BCFA-430C-9680-24E5843A3ED0
instance of	Homo sapiens
ResearchGate profile ID	wds:Q46130607-3be89a9b-4fd4-53d0-7911-f7ea7f6b5790
ResearchGate profile ID	Rachel_Wevrick
Google Scholar author ID	wds:Q46130607-f682367e-4814-c12b-b203-e64ad9ee8bea
Google Scholar author ID	uySVAsIAAAAJ
occupation	wds:Q46130607-16249A08-E10A-4CD3-93C9-851FBA72F65A wds:Q46130607-b31c9e4a-4532-76fa-c882-c6f142ea24d7
employer	wds:Q46130607-0875e7fd-44a7-2bd0-de9f-49017e48e242
Canadiana Authorities ID (former scheme)	wds:Q46130607-b961ff06-4146-f3ea-f6b4-9e54ee5ac54b
sex or gender	wds:Q46130607-5B30AD22-F536-4C91-AD51-FB65842F270D
ISNI	wds:Q46130607-12eb7f46-43c4-20e6-9f73-cee6cc76a20b
VIAF ID	wds:Q46130607-99588353-4a0a-d379-36cb-6c5c2d6bcfdc
country of citizenship	wds:Q46130607-91407f70-41db-f4eb-e8a5-b31a38d6b5f6
date of birth	wds:Q46130607-8ad3ef39-4d56-5a2c-7984-47c179c3f309
educated at	wds:Q46130607-1dfa1dcf-46d6-7446-0b44-47c5723a653c wds:Q46130607-52ee4228-4ed7-42ae-1f4d-25cc29240896
family name	wds:Q46130607-10BAE71F-6C95-4673-87CA-4453C1D83A13
WorldCat Identities ID (superseded)	wds:Q46130607-DAB5C323-D02B-4C53-A71F-7F41AB93B040
Canadiana Name Authority ID	wds:Q46130607-4c366773-4151-b8fe-9e69-598e78c92e93
VIAF ID	http://viaf.org/viaf/105708686
occupation	professor geneticist
employer	University of Alberta
Canadiana Authorities ID (former scheme)	0072K2007
sex or gender	female organism
ISNI	0000000076256310
VIAF ID	105708686
country of citizenship	Malawi
date of birth	1965-01-01 00:00:00Z (xsd:dateTime)
educated at	University of Toronto Queen's University
family name	Wevrick
WorldCat Identities ID (superseded)	viaf-105708686
Canadiana Name Authority ID	ncf10344317
ORCID iD	wds:Q46130607-2665EA67-4C81-45BB-B495-A94F6136D30B
ORCID iD	https://orcid.org/0000-0002-3343-5794
ORCID iD	0000-0002-3343-5794
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q46130607
is author of	Cloning and analysis of the murine Fanconi anemia group C cDNA. Establishment and maintenance of DNA methylation patterns in mouse Ndn: implications for maintenance of imprinting in target genes of the imprinting center. Necdin, a p53 target gene, regulates the quiescence and response to genotoxic stress of hematopoietic stem/progenitor cells. The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse Disruption of the mouse necdin gene results in early post-natal lethality Diagnostic test for the Prader-Willi syndrome by SNRPN expression in blood A mouse model for Prader-Willi syndrome imprinting-centre mutations Human centromeric DNAs. The imprinted gene Magel2 regulates normal circadian output. Mapping of the murine and rat Facc genes and assessment of flexed-tail as a candidate mouse homolog of Fanconi anemia group C Loss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice Impaired hypothalamic regulation of endocrine function and delayed counterregulatory response to hypoglycemia in Magel2-null mice. Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development. Regionally reduced brain volume, altered serotonin neurochemistry, and abnormal behavior in mice null for the circadian rhythm output gene Magel2. Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7. Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain.

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