Detalhe da pesquisa
1.
Unraveling the genetics of arsenic toxicity with cellular morphology QTL.
PLoS Genet
; 20(4): e1011248, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38662777
2.
Genetic control of the pluripotency epigenome determines differentiation bias in mouse embryonic stem cells.
EMBO J
; 41(2): e109445, 2022 12 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-34931323
3.
Spindle assembly checkpoint insensitivity allows meiosis-II despite chromosomal defects in aged eggs.
EMBO Rep
; 24(11): e57227, 2023 11 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37795949
4.
Mouse Genetic Reference Populations: Cellular Platforms for Integrative Systems Genetics.
Trends Genet
; 37(3): 251-265, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33010949
5.
The spontaneous mouse mutant low set ears (Lse) is caused by tandem duplication of Fgf3 and Fgf4.
Mamm Genome
; 34(3): 453-463, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37341808
6.
High-Diversity Mouse Populations for Complex Traits.
Trends Genet
; 35(7): 501-514, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31133439
7.
Large-scale discovery of mouse transgenic integration sites reveals frequent structural variation and insertional mutagenesis.
Genome Res
; 29(3): 494-505, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30659012
8.
The Mutant Mouse Resource and Research Center (MMRRC): the NIH-supported National Public Repository and Distribution Archive of Mutant Mouse Models in the USA.
Mamm Genome
; 33(1): 203-212, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34313795
9.
Global genetic analysis in mice unveils central role for cilia in congenital heart disease.
Nature
; 521(7553): 520-4, 2015 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-25807483
10.
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy.
Hum Mol Genet
; 26(24): 4937-4950, 2017 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29040572
11.
ENU-induced mutant allele of Dnah1, ferf1, causes abnormal sperm behavior and fertilization failure in mice.
Mol Reprod Dev
; 86(4): 416-425, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30734403
12.
Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders.
Genome Res
; 25(7): 948-57, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25917818
13.
Biallelic mutations in FDXR cause neurodegeneration associated with inflammation.
J Hum Genet
; 63(12): 1211-1222, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30250212
14.
Discovery and characterization of spontaneous mouse models of craniofacial dysmorphology.
Dev Biol
; 415(2): 216-227, 2016 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26234751
15.
A missense mutation in Grm6 reduces but does not eliminate mGluR6 expression or rod depolarizing bipolar cell function.
J Neurophysiol
; 118(2): 845-854, 2017 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28490646
16.
CRISPRtools: a flexible computational platform for performing CRISPR/Cas9 experiments in the mouse.
Mamm Genome
; 28(7-8): 283-290, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28280930
17.
Mouse genomic variation and its effect on phenotypes and gene regulation.
Nature
; 477(7364): 289-94, 2011 Sep 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-21921910
18.
Kif18a is specifically required for mitotic progression during germ line development.
Dev Biol
; 402(2): 253-262, 2015 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25824710
19.
Nuclear localization of PRDM9 and its role in meiotic chromatin modifications and homologous synapsis.
Chromosoma
; 124(3): 397-415, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25894966
20.
Dsp rul: a spontaneous mouse mutation in desmoplakin as a model of Carvajal-Huerta syndrome.
Exp Mol Pathol
; 98(2): 164-72, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25659760