A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse
about
The mouse genetics toolkit: revealing function and mechanismUnderstanding mammalian genetic systems: the challenge of phenotyping in the mouseProgress in genetic studies of pain and analgesial7Rn6 encodes a novel protein required for clara cell function in mouse lung developmentMouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics ProjectThe European dimension for the mouse genome mutagenesis programConstitutional downregulation of SEMA5A expression in autismAn ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathyDiphthamide modification of eEF2 requires a J-domain protein and is essential for normal developmentThrombocytopenia and kidney disease in mice with a mutation in the C1galt1 geneFocusing on the genetics of hearing: you ain't heard nothin' yet.A focused and efficient genetic screening strategy in the mouse: identification of mutations that disrupt cortical developmentA7DB: a relational database for mutational, physiological and pharmacological data related to the alpha7 nicotinic acetylcholine receptorIntraocular pressure in genetically distinct mice: an update and strain surveyThe trappist's approach to pathfinding: elucidating brain wiring using secretory-trap mutagenesisIdentification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging techniqueARTS: a web-based tool for the set-up of high-throughput genome-wide mapping panels for the SNP genotyping of mouse mutants.Efficient gene-driven germ-line point mutagenesis of C57BL/6J miceThe Snark was a Boojum - reloadedCurrent strategies for mutation detection in phenotype-driven screens utilising next generation sequencingDissecting immunity by germline mutagenesisModelling age-related metabolic disorders in the mouseMutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypesNovel gene function revealed by mouse mutagenesis screens for models of age-related disease.Mutant glycyl-tRNA synthetase (Gars) ameliorates SOD1(G93A) motor neuron degeneration phenotype but has little affect on Loa dynein heavy chain mutant miceMouse models for human otitis mediaInsertional mutagenesis in mice: new perspectives and toolsMutations in the Gabrb1 gene promote alcohol consumption through increased tonic inhibitionA mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutationScreening for increased plasma urea levels in a large-scale ENU mouse mutagenesis project reveals kidney disease modelsEffects of G-protein mutations on skin colorMutation of l7Rn3 shows that Odz4 is required for mouse gastrulationDissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen.Role of the transcription factor sox4 in insulin secretion and impaired glucose toleranceMutations in Mll2, an H3K4 methyltransferase, result in insulin resistance and impaired glucose tolerance in miceN-ethyl-N-Nitrosourea (ENU) induced mutations within the klotho gene lead to ectopic calcification and reduced lifespan in mouse modelsSignaling through the TGF beta-activin receptors ALK4/5/7 regulates testis formation and male germ cell developmentMutation at the Evi1 locus in Junbo mice causes susceptibility to otitis mediaAn ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant YodaIdentification of a novel point mutation of mouse proto-oncogene c-kit through N-ethyl-N-nitrosourea mutagenesis
P2860
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P2860
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse
description
2000 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
articolo scientifico
@it
artículu científicu espublizáu en 2000
@ast
im August 2000 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2000/08/01)
@sk
vědecký článek publikovaný v roce 2000
@cs
wetenschappelijk artikel (gepubliceerd op 2000/08/01)
@nl
наукова стаття, опублікована в серпні 2000
@uk
name
A systematic, genome-wide, phe ...... function studies in the mouse
@ast
A systematic, genome-wide, phe ...... function studies in the mouse
@en
A systematic, genome-wide, phe ...... function studies in the mouse
@nl
type
label
A systematic, genome-wide, phe ...... function studies in the mouse
@ast
A systematic, genome-wide, phe ...... function studies in the mouse
@en
A systematic, genome-wide, phe ...... function studies in the mouse
@nl
prefLabel
A systematic, genome-wide, phe ...... function studies in the mouse
@ast
A systematic, genome-wide, phe ...... function studies in the mouse
@en
A systematic, genome-wide, phe ...... function studies in the mouse
@nl
P2093
P921
P356
P1433
P1476
A systematic, genome-wide, phe ...... function studies in the mouse
@en
P2093
A. Kiernan
C. Nickols
C. Thornton
D. Brooker
E. M. Fisher
P2888
P304
P356
10.1038/78140
P407
P577
2000-08-01T00:00:00Z
P6179
1019613304