Detalhe da pesquisa
1.
Centriolar satellites are assembly points for proteins implicated in human ciliopathies, including oral-facial-digital syndrome 1.
J Cell Sci
; 124(Pt 4): 600-12, 2011 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21266464
2.
Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities.
Am J Hum Genet
; 84(2): 197-209, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19200523
3.
Convergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome gene.
Hum Mol Genet
; 18(2): 289-303, 2009 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18971206
4.
Molecular characterization and expression analysis of Mtmr2, mouse homologue of MTMR2, the Myotubularin-related 2 gene, mutated in CMT4B.
Gene
; 283(1-2): 17-26, 2002 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-11867209
5.
Correction of G551D-CFTR transport defect in epithelial monolayers by genistein but not by CPX or MPB-07.
Br J Pharmacol
; 137(4): 504-12, 2002 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12359632
6.
OFD1 is a centrosomal/basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis.
J Am Soc Nephrol
; 15(10): 2556-68, 2004 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-15466260
7.
IL-4 is a potent modulator of ion transport in the human bronchial epithelium in vitro.
J Immunol
; 168(2): 839-45, 2002 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-11777980
8.
OFD1, the gene mutated in oral-facial-digital syndrome type 1, is expressed in the metanephros and in human embryonic renal mesenchymal cells.
J Am Soc Nephrol
; 14(3): 680-9, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12595504