Detalhe da pesquisa
1.
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disorders.
medRxiv
; 2023 Dec 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38234731
2.
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.
Nat Genet
; 55(7): 1149-1163, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37386251
3.
The HSPGs Syndecan and Dallylike bind the receptor phosphatase LAR and exert distinct effects on synaptic development.
Neuron
; 49(4): 517-31, 2006 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-16476662
4.
Etv1 Controls the Establishment of Non-overlapping Motor Innervation of Neighboring Facial Muscles during Development.
Cell Rep
; 29(2): 437-452.e4, 2019 10 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31597102
5.
Loss of CXCR4/CXCL12 Signaling Causes Oculomotor Nerve Misrouting and Development of Motor Trigeminal to Oculomotor Synkinesis.
Invest Ophthalmol Vis Sci
; 59(12): 5201-5209, 2018 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30372748
6.
Mutant α2-chimaerin signals via bidirectional ephrin pathways in Duane retraction syndrome.
J Clin Invest
; 127(5): 1664-1682, 2017 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28346224
7.
Proteoglycan-specific molecular switch for RPTPσ clustering and neuronal extension.
Science
; 332(6028): 484-8, 2011 Apr 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-21454754
8.
PTPsigma is a receptor for chondroitin sulfate proteoglycan, an inhibitor of neural regeneration.
Science
; 326(5952): 592-6, 2009 Oct 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-19833921