Detalhe da pesquisa
1.
Defective signaling through plexin-A1 compromises the development of the peripheral olfactory system and neuroendocrine reproductive axis in mice.
Hum Mol Genet
; 26(11): 2006-2017, 2017 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28334861
2.
Meis1 coordinates a network of genes implicated in eye development and microphthalmia.
Development
; 142(17): 3009-20, 2015 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26253404
3.
Secreted frizzled related proteins modulate pathfinding and fasciculation of mouse retina ganglion cell axons by direct and indirect mechanisms.
J Neurosci
; 35(11): 4729-40, 2015 Mar 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-25788689
4.
Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness.
Am J Hum Genet
; 92(5): 707-24, 2013 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23643381
5.
Differential roles of Netrin-1 and its receptor DCC in inferior olivary neuron migration.
Mol Cell Neurosci
; 41(4): 429-39, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19409494
6.
The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.
J Clin Endocrinol Metab
; 99(10): E2138-43, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25077900
7.
The vesicular SNARE Synaptobrevin is required for Semaphorin 3A axonal repulsion.
J Cell Biol
; 196(1): 37-46, 2012 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-22213797
8.
SFRPs act as negative modulators of ADAM10 to regulate retinal neurogenesis.
Nat Neurosci
; 14(5): 562-9, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21478884
9.
Tubulin tyrosination is required for the proper organization and pathfinding of the growth cone.
PLoS One
; 4(4): e5405, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19404406
10.
Expression, purification and preliminary crystallographic studies of a single-point mutant of Mos1 mariner transposase.
Acta Crystallogr D Biol Crystallogr
; 60(Pt 5): 962-4, 2004 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15103153