Detalhe da pesquisa
1.
Ciliary Doublet Microtubules at Near-Atomic Resolution.
Cell
; 179(4): 805-807, 2019 10 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-31675493
2.
CapSeq and CIP-TAP identify Pol II start sites and reveal capped small RNAs as C. elegans piRNA precursors.
Cell
; 151(7): 1488-500, 2012 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-23260138
3.
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
4.
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
5.
Arih2 regulates Hedgehog signaling through smoothened ubiquitylation and ER-associated degradation.
J Cell Sci
; 135(16)2022 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35899529
6.
A cAMP signalosome in primary cilia drives gene expression and kidney cyst formation.
EMBO Rep
; 23(8): e54315, 2022 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35695071
7.
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
8.
Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract.
Kidney Int
; 101(5): 1039-1053, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35227688
9.
A global analysis of IFT-A function reveals specialization for transport of membrane-associated proteins into cilia.
J Cell Sci
; 132(3)2019 02 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30659111
10.
Global genetic analysis in mice unveils central role for cilia in congenital heart disease.
Nature
; 521(7553): 520-4, 2015 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-25807483
11.
Abnormal fertility, acrosome formation, IFT20 expression and localization in conditional Gmap210 knockout mice.
Am J Physiol Cell Physiol
; 318(1): C174-C190, 2020 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31577511
12.
Loss of Arf4 causes severe degeneration of the exocrine pancreas but not cystic kidney disease or retinal degeneration.
PLoS Genet
; 13(4): e1006740, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28410364
13.
Intraflagellar transport protein 74 is essential for spermatogenesis and male fertility in mice.
Biol Reprod
; 101(1): 188-199, 2019 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31004481
14.
IFT20 controls LAT recruitment to the immune synapse and T-cell activation in vivo.
Proc Natl Acad Sci U S A
; 113(2): 386-91, 2016 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26715756
15.
DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia.
PLoS Genet
; 12(2): e1005821, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26918822
16.
Intraflagellar transporter protein (IFT27), an IFT25 binding partner, is essential for male fertility and spermiogenesis in mice.
Dev Biol
; 432(1): 125-139, 2017 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28964737
17.
Intraflagellar transport 27 is essential for hedgehog signaling but dispensable for ciliogenesis during hair follicle morphogenesis.
Development
; 142(12): 2194-202, 2015 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26023097
18.
Ciliary proteins Bbs8 and Ift20 promote planar cell polarity in the cochlea.
Development
; 142(3): 555-66, 2015 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25605782
19.
Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes.
J Med Genet
; 54(6): 371-380, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28289185
20.
Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies.
Hum Mol Genet
; 24(14): 3994-4005, 2015 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25877302