Detalhe da pesquisa
1.
Autonomous and non-cell autonomous role of cilia in structural birth defects in mice.
PLoS Biol
; 21(12): e3002425, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38079449
2.
IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans.
PLoS Genet
; 19(6): e1010796, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37315079
3.
c-Jun N-terminal kinase (JNK) signaling contributes to cystic burden in polycystic kidney disease.
PLoS Genet
; 17(12): e1009711, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34962918
4.
Arf4 is required for Mammalian development but dispensable for ciliary assembly.
PLoS Genet
; 10(2): e1004170, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24586199
5.
Disruption of IFT complex A causes cystic kidneys without mitotic spindle misorientation.
J Am Soc Nephrol
; 23(4): 641-51, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22282595
6.
The Tumor-Associated Calcium Signal Transducer 2 (TACSTD2) oncogene is upregulated in pre-cystic epithelial cells revealing a new target for polycystic kidney disease.
medRxiv
; 2023 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38106222
7.
Autonomous and non-cell autonomous etiology of ciliopathy associated structural birth defects.
bioRxiv
; 2023 Jun 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37333142
8.
IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans.
medRxiv
; 2023 Feb 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-36865301
9.
c-JUN n-Terminal Kinase (JNK) Signaling in Autosomal Dominant Polycystic Kidney Disease.
J Cell Signal
; 3(1): 62-78, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35253003
10.
The Golgin GMAP210/TRIP11 anchors IFT20 to the Golgi complex.
PLoS Genet
; 4(12): e1000315, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19112494
11.
Ift25 is not a cystic kidney disease gene but is required for early steps of kidney development.
Mech Dev
; 151: 10-17, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29626631
12.
Genetic link between renal birth defects and congenital heart disease.
Nat Commun
; 7: 11103, 2016 Mar 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-27002738
13.
Mechanisms mediating oxalate-induced alterations in renal cell functions.
Crit Rev Eukaryot Gene Expr
; 13(1): 55-72, 2003.
Artigo
em Inglês
| MEDLINE | ID: mdl-12839097
14.
How elevated oxalate can promote kidney stone disease: changes at the surface and in the cytosol of renal cells that promote crystal adherence and growth.
Front Biosci
; 9: 797-808, 2004 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-14766409
15.
Identification of physician and patient attributes that influence the likelihood of screening for intimate partner violence.
Acad Med
; 78(10 Suppl): S20-3, 2003 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-14557085
16.
Intracellular events in the initiation of calcium oxalate stones.
Nephron Exp Nephrol
; 98(2): e61-4, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15499209
17.
IFT27 links the BBSome to IFT for maintenance of the ciliary signaling compartment.
Dev Cell
; 31(3): 279-290, 2014 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-25446516
18.
IFT25 links the signal-dependent movement of Hedgehog components to intraflagellar transport.
Dev Cell
; 22(5): 940-51, 2012 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22595669
19.
Erratum: Genetic link between renal birth defects and congenital heart disease.
Nat Commun
; 7: 11910, 2016 06 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27273704
20.
Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease.
J Cell Biol
; 183(3): 377-84, 2008 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-18981227