Detalhe da pesquisa
1.
Mutant cohesin in premature ovarian failure.
N Engl J Med
; 370(10): 943-949, 2014 Mar 06.
Artigo
Inglês
| MEDLINE | ID: mdl-24597867
2.
The candidate splicing factor Sfswap regulates growth and patterning of inner ear sensory organs.
PLoS Genet
; 10(1): e1004055, 2014 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-24391519
3.
Histone posttranslational modifications and cell fate determination: lens induction requires the lysine acetyltransferases CBP and p300.
Nucleic Acids Res
; 41(22): 10199-214, 2013 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-24038357
4.
Transposon mutagenesis with coat color genotyping identifies an essential role for Skor2 in sonic hedgehog signaling and cerebellum development.
Development
; 138(20): 4487-97, 2011 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-21937600
5.
A transgenic insertion on mouse chromosome 17 inactivates a novel immunoglobulin superfamily gene potentially involved in sperm-egg fusion.
Mamm Genome
; 25(3-4): 141-8, 2014 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-24275887
6.
Intracorneal positioning of the lens in Pax6-GAL4/VP16 transgenic mice.
Mol Vis
; 11: 876-86, 2005 Oct 26.
Artigo
Inglês
| MEDLINE | ID: mdl-16270027
7.
A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosis.
PLoS One
; 7(11): e50634, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-23226340
8.
Head bobber: an insertional mutation causes inner ear defects, hyperactive circling, and deafness.
J Assoc Res Otolaryngol
; 13(3): 335-49, 2012 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-22383091
9.
Multiple autism-like behaviors in a novel transgenic mouse model.
Behav Brain Res
; 218(1): 29-41, 2011 Mar 17.
Artigo
Inglês
| MEDLINE | ID: mdl-21093492
10.
A mutation in the inner mitochondrial membrane peptidase 2-like gene (Immp2l) affects mitochondrial function and impairs fertility in mice.
Biol Reprod
; 78(4): 601-10, 2008 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-18094351
11.
Generation of rat mutants using a coat color-tagged Sleeping Beauty transposon system.
Mamm Genome
; 18(5): 338-46, 2007 May.
Artigo
Inglês
| MEDLINE | ID: mdl-17557177
12.
Genetic mapping of an insertional hydrocephalus-inducing mutation allelic to hy3.
Mamm Genome
; 13(11): 625-32, 2002 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-12461648
13.
exma: an X-linked insertional mutation that disrupts forebrain and eye development.
Mamm Genome
; 13(4): 179-85, 2002 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-11956759