about
Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypesComparative mapping of the imprinted U2afbpL gene on mouse chromosome 11 and human chromosome 5A Sox10 expression screen identifies an amino acid essential for Erbb3 function.A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathyThe exon junction complex component Magoh controls brain size by regulating neural stem cell division.Comparison of melanoblast expression patterns identifies distinct classes of genesMethod of euthanasia influences the oocyte fertilization rate with fresh mouse sperm.Ectopic differentiation of melanocyte stem cells is influenced by genetic background.Genomic analysis reveals distinct mechanisms and functional classes of SOX10-regulated genes in melanocytes.Microarray expression analysis and identification of serum biomarkers for Niemann-Pick disease, type C1.The transcription factors Ets1 and Sox10 interact during murine melanocyte development.Genomic copy number and expression variation within the C57BL/6J inbred mouse strainA unique missense allele of BAF155, a core BAF chromatin remodeling complex protein, causes neural tube closure defects in mice.Construction of a 3-Mb contig and partial transcript map of the central region of mouse chromosome 11.Efficacy of N-acetylcysteine in phenotypic suppression of mouse models of Niemann-Pick disease, type C1.SOX10 ablation arrests cell cycle, induces senescence, and suppresses melanomagenesisHighly Efficient Cpf1-Mediated Gene Targeting in Mice Following High Concentration Pronuclear Injection.Correction: Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes.Generation of RCAS vectors useful for functional genomic analyses.Loci associated with skin pigmentation identified in African populations.Genetic mapping of 21 genes on mouse chromosome 11 reveals disruptions in linkage conservation with human chromosome 5.How many homeobox genes does it take to make a pituitary gland?Persistent Prop1 expression delays gonadotrope differentiation and enhances pituitary tumor susceptibility.Linkage mapping of murine homolog of the yeast SPT6 gene to MMU11B1.In utero complementation of a neural crest-derived melanocyte defect using cell directed gene transferEncyclopedia of the mouse genome V. Mouse chromosome 11
P50
Q27329518-B19480E9-3D05-400E-A209-028049615A41Q28240346-5FD661BF-95BB-47A8-A93E-0D26E93D187DQ28473562-E255382A-9409-40D3-B5DD-98B65AD9B894Q28590547-CB65D1A2-CD15-4361-8F08-D26133D1F618Q33814636-1C2D72D2-2883-480C-8B7F-4E71EF2FA913Q34428830-2EDDDDCE-9A9B-4E7E-A7B4-F121B92288F3Q34620024-581C9208-55BC-490E-B848-7186FE0F5A03Q35097045-6A11CB6E-FA7B-43B0-99B1-202A50B97495Q36065451-60ABAEFA-2244-4AC9-A30D-79BA3A052EFDQ36122424-1B42F756-925D-4848-8A4B-C436B58A6F12Q36202037-A896C860-AC19-4D83-B437-845BCE8EE3C6Q36259308-DE87F2AC-DE1C-4C61-83B5-B94CA743D57AQ36349016-565F13B1-140F-4348-9A9B-78E2048D013CQ36887115-E4714CE8-58C5-479A-BAD4-D43ACAE16F74Q37078859-2737D43E-75AF-4439-A4AE-D08401190F57Q37243181-7C568C45-2C02-4F45-8BB7-544EC9C6E882Q37629353-605A9034-D7C9-4670-82FA-2FE5FD346338Q43164337-8C5DE5A9-456A-464A-BC10-BA1D1D14223DQ43826373-3DF20C9A-1C1D-45BA-A4AF-642244C43DE3Q43924342-22B76867-9154-496D-9C99-67A817F36280Q48053825-1CF587D1-A19F-4115-A3F9-DC74043784DFQ48424256-4222D9CA-2A52-4389-8C4E-40832AF2DEE7Q48871210-708F40BB-62BB-4DDE-A1D6-5330DC2F6C21Q49010210-35075F5A-7B3A-4459-8B9D-4A8C9040659BQ63433368-71CB5539-C934-4766-83D0-B0E3B4549A4AQ63433369-AC5B67E5-0F55-4F63-8D87-CC58CF2A4EA4
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Dawn E Watkins-Chow
@ast
Dawn E Watkins-Chow
@en
Dawn E Watkins-Chow
@es
Dawn E Watkins-Chow
@nl
type
label
Dawn E Watkins-Chow
@ast
Dawn E Watkins-Chow
@en
Dawn E Watkins-Chow
@es
Dawn E Watkins-Chow
@nl
prefLabel
Dawn E Watkins-Chow
@ast
Dawn E Watkins-Chow
@en
Dawn E Watkins-Chow
@es
Dawn E Watkins-Chow
@nl
P106
P21
P31
P496
0000-0002-4355-0868