Detalhe da pesquisa
1.
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Nature;
526(7571): 112-7, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26367794
2.
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes.
Nature;
491(7424): 399-405, 2012 Nov 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23103869
3.
Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects.
Hum Mol Genet;
24(5): 1234-42, 2015 Mar 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25343988
4.
Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60.
Am J Hum Genet;
93(3): 515-23, 2013 Sep 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23910462
5.
Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy.
Am J Hum Genet;
93(5): 932-44, 2013 Nov 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24183451
6.
Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans.
Am J Hum Genet;
93(5): 915-25, 2013 Nov 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24140113
7.
Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6.
Hum Mol Genet;
22(8): 1625-31, 2013 Apr 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23335591
8.
Deep-transcriptome and ribonome sequencing redefines the molecular networks of pluripotency and the extracellular space in human embryonic stem cells.
Genome Res;
21(12): 2014-25, 2011 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22042643
9.
Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas.
Clin Endocrinol (Oxf);
80(1): 25-33, 2014 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24102379
10.
A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells.
Genome Res;
20(8): 1052-63, 2010 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20508144
11.
Regulated post-transcriptional RNA cleavage diversifies the eukaryotic transcriptome.
Genome Res;
20(12): 1639-50, 2010 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21045082
12.
Refining transcriptional programs in kidney development by integration of deep RNA-sequencing and array-based spatial profiling.
BMC Genomics;
12: 441, 2011 Sep 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21888672
13.
Stem cell transcriptome profiling via massive-scale mRNA sequencing.
Nat Methods;
5(7): 613-9, 2008 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18516046
14.
Kidney transcriptome reveals altered steroid homeostasis in NaS1 sulfate transporter null mice.
J Steroid Biochem Mol Biol;
112(1-3): 55-62, 2008 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18790054
15.
Transcriptional analysis of early lineage commitment in human embryonic stem cells.
BMC Dev Biol;
7: 12, 2007 Mar 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17335568
16.
Dynamic transcription programs during ES cell differentiation towards mesoderm in serum versus serum-freeBMP4 culture.
BMC Genomics;
8: 365, 2007 Oct 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17925037
17.
Osteonectin downregulates E-cadherin, induces osteopontin and focal adhesion kinase activity stimulating an invasive melanoma phenotype.
Int J Cancer;
121(12): 2653-60, 2007 Dec 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17724718
18.
Transcriptional profile reveals altered hepatic lipid and cholesterol metabolism in hyposulfatemic NaS1 null mice.
Physiol Genomics;
26(2): 116-24, 2006 Jul 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16621889
19.
Spatial gene expression in the T-stage mouse metanephros.
Gene Expr Patterns;
6(8): 807-25, 2006 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16545622
20.
Osteonectin/SPARC induction by ectopic beta(3) integrin in human radial growth phase primary melanoma cells.
Cancer Res;
62(1): 226-32, 2002 Jan 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-11782382