Detalhe da pesquisa
1.
HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutants.
PLoS Genet
; 7(10): e1002336, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22028672
2.
A Wars2 mutant mouse shows a sex and diet specific change in fat distribution, reduced food intake and depot-specific upregulation of WAT browning.
Front Physiol
; 13: 953199, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36091365
3.
Zfhx3-mediated genetic ablation of the SCN abolishes light entrainable circadian activity while sparing food anticipatory activity.
iScience
; 24(10): 103142, 2021 Oct 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34632336
4.
Dedicated mouse production and husbandry.
Methods Mol Biol
; 561: 285-99, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19504079
5.
Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2.
J Bone Miner Res
; 22(9): 1397-407, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17539739
6.
Inducible Knockout of Mouse Zfhx3 Emphasizes Its Key Role in Setting the Pace and Amplitude of the Adult Circadian Clock.
J Biol Rhythms
; 32(5): 433-443, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28816086
7.
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse.
J Neurosci
; 23(5): 1631-7, 2003 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12629167
8.
Dominant ß-catenin mutations cause intellectual disability with recognizable syndromic features.
J Clin Invest
; 124(4): 1468-82, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24614104
9.
Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal development.
J Cell Sci
; 121(Pt 19): 3140-5, 2008 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18765564
10.
Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathy.
Mol Cell Neurosci
; 21(1): 114-25, 2002 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-12359155
11.
Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse.
Comp Funct Genomics
; 5(2): 123-7, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-18629060
12.
A gene-driven ENU-based approach to generating an allelic series in any gene.
Mamm Genome
; 15(8): 585-91, 2004 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-15457338
13.
Novel phenotypes identified by plasma biochemical screening in the mouse.
Mamm Genome
; 13(10): 595-602, 2002 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12420138