Detalhe da pesquisa
1.
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes.
Cell
; 154(2): 452-64, 2013 Jul 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-23870131
2.
Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration.
Hum Mol Genet
; 25(2): 291-307, 2016 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26604141
3.
Gray platelet syndrome: proinflammatory megakaryocytes and α-granule loss cause myelofibrosis and confer metastasis resistance in mice.
Blood
; 124(24): 3624-35, 2014 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-25258341
4.
Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndrome.
Am J Hum Genet
; 91(6): 998-1010, 2012 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23200864
5.
Disruption of mouse Cenpj, a regulator of centriole biogenesis, phenocopies Seckel syndrome.
PLoS Genet
; 8(11): e1003022, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23166506
6.
The critical role of histone H2A-deubiquitinase Mysm1 in hematopoiesis and lymphocyte differentiation.
Blood
; 119(6): 1370-9, 2012 Feb 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-22184403
7.
The role of sphingosine-1-phosphate transporter Spns2 in immune system function.
J Immunol
; 189(1): 102-11, 2012 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22664872
8.
Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1.
Mamm Genome
; 24(1-2): 44-53, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23160729
9.
High-fat feeding rapidly induces obesity and lipid derangements in C57BL/6N mice.
Mamm Genome
; 24(5-6): 240-51, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23712496
10.
A gene expression resource generated by genome-wide lacZ profiling in the mouse.
Dis Model Mech
; 8(11): 1467-78, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26398943
11.
Programmed cell death in Xenopus laevis spinal cord, tail and other tissues, prior to, and during, metamorphosis.
Life Sci
; 73(25): 3297-306, 2003 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-14561534
12.
Histopathology reveals correlative and unique phenotypes in a high-throughput mouse phenotyping screen.
Dis Model Mech
; 7(5): 515-24, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24652767
13.
Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen.
Nat Commun
; 5: 3540, 2014 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-24721909
14.
Targeting of Slc25a21 is associated with orofacial defects and otitis media due to disrupted expression of a neighbouring gene.
PLoS One
; 9(3): e91807, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24642684
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.
The distribution of vasotocin and mesotocin immunoreactivity in the hypothalamic magnocellular neurosecretory nuclei of the Saharan herbivorous lizard, Uromastix acanthinurus Bell, 1825 (Sauria-Agamidae).
Histol Histopathol
; 25(2): 159-75, 2010 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-20017103