Detalhe da pesquisa
1.
KATNAL1 regulation of sertoli cell microtubule dynamics is essential for spermiogenesis and male fertility.
PLoS Genet
; 8(5): e1002697, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22654668
2.
Identification of an imprinting control region affecting the expression of all transcripts in the Gnas cluster.
Nat Genet
; 38(3): 350-5, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16462745
3.
The novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity in the ear.
BMC Dev Biol
; 10: 87, 2010 Aug 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-20704721
4.
Single primer amplification (SPA) of cDNA for microarray expression analysis.
Nucleic Acids Res
; 31(3): e9, 2003 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12560512
5.
Mouse mutagenesis identifies novel roles for left-right patterning genes in pulmonary, craniofacial, ocular, and limb development.
Dev Dyn
; 238(3): 581-94, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19235720
6.
VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5.
Genes Dev
; 22(11): 1465-77, 2008 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18519639
7.
The after-hours mutant reveals a role for Fbxl3 in determining mammalian circadian period.
Science
; 316(5826): 897-900, 2007 May 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-17463252
8.
A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse.
Hum Mol Genet
; 15(22): 3273-9, 2006 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17035249
9.
New semidominant mutations that affect mouse development.
Genesis
; 40(2): 109-117, 2004 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-15384171
10.
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
11.
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