Detalhe da pesquisa
1.
Fgf-driven Tbx protein activities directly induce myf5 and myod to initiate zebrafish myogenesis.
Development
; 147(8)2020 04 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32345657
2.
Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24.
Hum Mol Genet
; 28(11): 1919-1929, 2019 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30715372
3.
Bi-allelic mutations in MYL1 cause a severe congenital myopathy.
Hum Mol Genet
; 27(24): 4263-4272, 2018 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30215711
4.
Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy.
Am J Hum Genet
; 100(3): 537-545, 2017 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28190459
5.
The Bardet-Biedl syndrome-related protein CCDC28B modulates mTORC2 function and interacts with SIN1 to control cilia length independently of the mTOR complex.
Hum Mol Genet
; 22(20): 4031-42, 2013 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23727834
6.
Heat shock induces rapid resorption of primary cilia.
J Cell Sci
; 125(Pt 18): 4297-305, 2012 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22718348
7.
Characterization of CCDC28B reveals its role in ciliogenesis and provides insight to understand its modifier effect on Bardet-Biedl syndrome.
Hum Genet
; 132(1): 91-105, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23015189
8.
Cdkn1c drives muscle differentiation through a positive feedback loop with Myod.
Dev Biol
; 350(2): 464-75, 2011 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21147088
9.
Bbs8, together with the planar cell polarity protein Vangl2, is required to establish left-right asymmetry in zebrafish.
Dev Biol
; 345(2): 215-25, 2010 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20643117
10.
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia.
Nat Commun
; 10(1): 4790, 2019 10 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-31636353
11.
Vestigial-like-2b (VITO-1b) and Tead-3a (Tef-5a) expression in zebrafish skeletal muscle, brain and notochord.
Gene Expr Patterns
; 7(8): 827-36, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17916448
12.
Mrf4 (myf6) is dynamically expressed in differentiated zebrafish skeletal muscle.
Gene Expr Patterns
; 7(7): 738-45, 2007 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-17638597
13.
Zebrafish: a vertebrate tool for studying basal body biogenesis, structure, and function.
Cilia
; 5: 16, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27168933
14.
Evaluation of zebrafish kidney function using a fluorescent clearance assay.
J Vis Exp
; (96): e52540, 2015 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-25742415
15.
Loss of FTO antagonises Wnt signaling and leads to developmental defects associated with ciliopathies.
PLoS One
; 9(2): e87662, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24503721
16.
Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome.
Nat Genet
; 43(3): 197-203, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21258343
17.
Differential requirements for myogenic regulatory factors distinguish medial and lateral somitic, cranial and fin muscle fibre populations.
Development
; 136(3): 403-14, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19141670
18.
Basal body stability and ciliogenesis requires the conserved component Poc1.
J Cell Biol
; 187(6): 905-20, 2009 Dec 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-20008567
19.
Signals and myogenic regulatory factors restrict pax3 and pax7 expression to dermomyotome-like tissue in zebrafish.
Dev Biol
; 302(2): 504-21, 2007 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17094960