About: Muriel Davisson

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

American neuroscientist

Attributes	Values
rdf:type	Item
owl:sameAs	Muriel Davisson
description	American neuroscientist (en) neurosiensiste american (lfn) usona neŭrosciencisto (eo) Amerikaans neurowetenschapster (nl) neurocientífica estadounidense (es) neurocientífica estauxunidense (ast) عالمة أعصاب من الولايات المتحدة الأمريكية (ar) neuroshkencëtar amerikane (sq) americká neurovědkyně (cs)
rdfs:label	Muriel Davisson (ca) Muriel Davisson (cs) Muriel Davisson (da) Muriel Davisson (de) Muriel Davisson (en) Muriel Davisson (es) Muriel Davisson (fi) Muriel Davisson (fr) Muriel Davisson (it) Muriel Davisson (nb) Muriel Davisson (nl) Muriel Davisson (pt) Muriel Davisson (sl) Muriel Davisson (pt-br) Muriel Davisson (ast)
skos:prefLabel	Muriel Davisson (ca) Muriel Davisson (cs) Muriel Davisson (da) Muriel Davisson (de) Muriel Davisson (en) Muriel Davisson (es) Muriel Davisson (fi) Muriel Davisson (fr) Muriel Davisson (it) Muriel Davisson (nb) Muriel Davisson (nl) Muriel Davisson (pt) Muriel Davisson (sl) Muriel Davisson (pt-br) Muriel Davisson (ast)
name	Muriel Davisson (ca) Muriel Davisson (cs) Muriel Davisson (da) Muriel Davisson (de) Muriel Davisson (en) Muriel Davisson (es) Muriel Davisson (fi) Muriel Davisson (fr) Muriel Davisson (it) Muriel Davisson (nb) Muriel Davisson (nl) Muriel Davisson (pt) Muriel Davisson (sl) Muriel Davisson (pt-br) Muriel Davisson (ast)
Freebase ID	wds:Q6938611-2041E81A-53AF-413B-B2B6-87BA471B495C
Freebase ID	/m/0h1d2cg
Scopus author ID	wds:Q6938611-0b86c760-46b1-028f-d3d4-4ee672a2d459
Scopus author ID	35376991200
given name	wds:Q6938611-9E4BC8F8-F590-42D8-8DA4-D51380B3C454
given name	Muriel
instance of	wds:Q6938611-8A4CEBF7-4A54-4576-9BEC-2E3FA45096D9
instance of	Homo sapiens
occupation	wds:Q6938611-93420978-C592-4821-B562-2328CBAEB7BD
sex or gender	wds:Q6938611-8DAC9254-4A44-4AC4-BEFA-81ABEE88A018
country of citizenship	wds:Q6938611-C575595F-BEA6-4259-9CC9-7D5F10C4B2A9
educated at	wds:Q6938611-C40747AE-E591-4735-BC1F-1F86FCB0D7F0
family name	wds:Q6938611-EA74CB7B-C98A-4117-88BF-209A7593504A
occupation	neuroscientist
sex or gender	female organism
country of citizenship	United States of America
educated at	Pennsylvania State University
family name	Davisson
is about of	Muriel Davisson https://www.wikidata.org/wiki/Special:EntityData/Q6938611 Muriel Davisson
is author of	Mouse model of subretinal neovascularization with choroidal anastomosis Kidney adysplasia and variable hydronephrosis, a new mutation affecting the odd-skipped related 1 gene in the mouse, causes variable defects in kidney development and hydronephrosis Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndrome A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration Building protein interaction maps for Down's syndrome Discovery genetics: serendipity in basic research The effects of piracetam on cognitive performance in a mouse model of Down's syndrome VAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P(2) in yeast and mouse Trak1 mutation disrupts GABA(A) receptor homeostasis in hypertonic mice The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses Know thy mouse A mouse model for Meckel syndrome type 3. Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10 New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice Differential effects of environmental enrichment on behavior and learning of male and female Ts65Dn mice, a model for Down syndrome. Behavioral validation of the Ts65Dn mouse model for Down syndrome of a genetic background free of the retinal degeneration mutation Pde6b(rd1). Otitis media in a mouse model for Down syndrome Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA). Centralized mouse repositories A-to-I pre-mRNA editing of the serotonin 2C receptor: comparisons among inbred mouse strains. Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouse Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions

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