Detalhe da pesquisa
1.
A holistic view of mouse enhancer architectures reveals analogous pleiotropic effects and correlation with human disease.
BMC Genomics
; 21(1): 754, 2020 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33138777
2.
A bioimage informatics platform for high-throughput embryo phenotyping.
Brief Bioinform
; 19(1): 41-51, 2018 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27742664
3.
The severity of retinal pathology in homozygous Crb1rd8/rd8 mice is dependent on additional genetic factors.
Hum Mol Genet
; 24(1): 128-41, 2015 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25147295
4.
Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project.
Mamm Genome
; 23(9-10): 600-10, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22961258
5.
MouseBook: an integrated portal of mouse resources.
Nucleic Acids Res
; 38(Database issue): D593-9, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19854936
6.
Making sense of the linear genome, gene function and TADs.
Epigenetics Chromatin
; 15(1): 4, 2022 01 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35090532
7.
Origin, specification and differentiation of a rare supporting-like lineage in the developing mouse gonad.
Sci Adv
; 8(21): eabm0972, 2022 May 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35613264
8.
Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes.
Dis Model Mech
; 14(10)2021 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34477842
9.
Phenotyping in Mice Using Continuous Home Cage Monitoring and Ultrasonic Vocalization Recordings.
Curr Protoc Mouse Biol
; 10(3): e80, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32813317
10.
Generation and Identification of Mutations Resulting in Chronic and Age-Related Phenotypes in Mice.
Curr Protoc Mouse Biol
; 8(2): e42, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29927552
11.
Prevalence of sexual dimorphism in mammalian phenotypic traits.
Nat Commun
; 8: 15475, 2017 06 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-28650954
12.
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.
Nat Commun
; 8(1): 886, 2017 10 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29026089
13.
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.
Nat Genet
; 49(8): 1231-1238, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28650483
14.
Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.
Nat Commun
; 7: 12444, 2016 08 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-27534441
15.
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.
Genome Biol
; 14(7): R82, 2013 Jul 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-23902802
16.
Finding and sharing: new approaches to registries of databases and services for the biomedical sciences.
Database (Oxford)
; 2010: baq014, 2010 Jul 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-20627863
17.
Mouse Phenotype Database Integration Consortium: integration [corrected] of mouse phenome data resources.
Mamm Genome
; 18(3): 157-63, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17436037
18.
CRAVE: a database, middleware and visualization system for phenotype ontologies.
Bioinformatics
; 21(7): 1257-62, 2005 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-15550481
19.
Towards a mutant map of the mouse--new models of neurological, behavioural, deafness, bone, renal and blood disorders.
Genetica
; 122(1): 47-9, 2004 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-15619960