Detalhe da pesquisa
1.
Renal impairment: an unnecessary barrier to HIV prevention.
Sex Health
; 17(3): 299-300, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32576363
2.
IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy.
Nat Genet
; 39(6): 727-9, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17468754
3.
BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus.
Nat Genet
; 38(5): 521-4, 2006 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-16582908
4.
Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney Disease.
Hum Mutat
; 34(5): 714-24, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23418020
5.
An Ift80 mouse model of short rib polydactyly syndromes shows defects in hedgehog signalling without loss or malformation of cilia.
Hum Mol Genet
; 20(7): 1306-14, 2011 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21227999
6.
Characteristics of recently arrived Asian men who have sex with men diagnosed with HIV through sexual health services in Melbourne and Sydney.
Aust N Z J Public Health
; 43(5): 424-428, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31287941
7.
CiliaCarta: An integrated and validated compendium of ciliary genes.
PLoS One
; 14(5): e0216705, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31095607
8.
Patterns of expression of Bardet-Biedl syndrome proteins in the mammalian cochlea suggest noncentrosomal functions.
J Comp Neurol
; 514(2): 174-88, 2009 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-19396898
9.
Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome.
Nat Genet
; 40(4): 443-8, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18327255