Detalhe da pesquisa
1.
The gene regulatory basis of genetic compensation during neural crest induction.
PLoS Genet
; 15(6): e1008213, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31199790
2.
A new patient-derived iPSC model for dystroglycanopathies validates a compound that increases glycosylation of α-dystroglycan.
EMBO Rep
; 20(11): e47967, 2019 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31566294
3.
Loss of the chromatin modifier Kdm2aa causes BrafV600E-independent spontaneous melanoma in zebrafish.
PLoS Genet
; 13(8): e1006959, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28806732
4.
A systematic genome-wide analysis of zebrafish protein-coding gene function.
Nature
; 496(7446): 494-7, 2013 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-23594742
5.
Alternative haplotypes of antigen processing genes in zebrafish diverged early in vertebrate evolution.
Proc Natl Acad Sci U S A
; 113(34): E5014-23, 2016 08 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-27493218
6.
The deubiquitinase USP9X suppresses pancreatic ductal adenocarcinoma.
Nature
; 486(7402): 266-70, 2012 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-22699621
7.
The Ribosome Biogenesis Protein Nol9 Is Essential for Definitive Hematopoiesis and Pancreas Morphogenesis in Zebrafish.
PLoS Genet
; 11(12): e1005677, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26624285
8.
New insights into the maternal to zygotic transition.
Development
; 141(20): 3834-41, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25294937
9.
The future of model organisms in human disease research.
Nat Rev Genet
; 12(8): 575-82, 2011 07 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-21765459
10.
A loss of function screen of identified genome-wide association study Loci reveals new genes controlling hematopoiesis.
PLoS Genet
; 10(7): e1004450, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25010335
11.
Zebrafish Rab5 proteins and a role for Rab5ab in nodal signalling.
Dev Biol
; 397(2): 212-24, 2015 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25478908
12.
Efficient identification of CRISPR/Cas9-induced insertions/deletions by direct germline screening in zebrafish.
BMC Genomics
; 17: 259, 2016 Mar 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-27009152
13.
Mutations in c10orf11, a melanocyte-differentiation gene, cause autosomal-recessive albinism.
Am J Hum Genet
; 92(3): 415-21, 2013 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23395477
14.
Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan.
Am J Hum Genet
; 93(1): 29-41, 2013 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-23768512
15.
Xenopus mutant reveals necessity of rax for specifying the eye field which otherwise forms tissue with telencephalic and diencephalic character.
Dev Biol
; 395(2): 317-330, 2014 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25224223
16.
High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping.
BMC Genomics
; 16: 578, 2015 Aug 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26238335
17.
Missense mutations in ß-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome.
Hum Mol Genet
; 22(9): 1746-54, 2013 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23359570
18.
Incorporating RNA-seq data into the zebrafish Ensembl genebuild.
Genome Res
; 22(10): 2067-78, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22798491
19.
Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function.
Acta Neuropathol
; 130(3): 389-406, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25931053
20.
Global identification of Smad2 and Eomesodermin targets in zebrafish identifies a conserved transcriptional network in mesendoderm and a novel role for Eomesodermin in repression of ectodermal gene expression.
BMC Biol
; 12: 81, 2014 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-25277163