Detalhe da pesquisa
1.
Multifaceted actions of Zeb2 in postnatal neurogenesis from the ventricular-subventricular zone to the olfactory bulb.
Development;
147(10)2020 05 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32253238
2.
Zeb2 Regulates Cell Fate at the Exit from Epiblast State in Mouse Embryonic Stem Cells.
Stem Cells;
35(3): 611-625, 2017 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27739137
3.
The Wnt/TCF7L1 transcriptional repressor axis drives primitive endoderm formation by antagonizing naive and formative pluripotency.
Nat Commun;
14(1): 1210, 2023 03 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36869101
4.
The C20orf133 gene is disrupted in a patient with Kabuki syndrome.
J Med Genet;
44(9): 562-9, 2007 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17586838
5.
Spontaneous Post-Transplant Disorders in NOD.Cg- Prkdcscid Il2rgtm1Sug/JicTac (NOG) Mice Engrafted with Patient-Derived Metastatic Melanomas.
PLoS One;
10(5): e0124974, 2015.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25996609
6.
Pathology in Practice. Opportunistic Pseudomonas aeruginosa infection as cause of otitis media and labyrinthitis in immunocompetent mice.
J Am Vet Med Assoc;
254(2): 221-224, 2019 Jan 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30605387
7.
Directed migration of cortical interneurons depends on the cell-autonomous action of Sip1.
Neuron;
77(1): 70-82, 2013 Jan 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23312517
8.
Stalk cell phenotype depends on integration of Notch and Smad1/5 signaling cascades.
Dev Cell;
22(3): 501-14, 2012 Mar 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22364862
9.
Few Smad proteins and many Smad-interacting proteins yield multiple functions and action modes in TGFß/BMP signaling in vivo.
Cytokine Growth Factor Rev;
22(5-6): 287-300, 2011.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22119658
10.
Essential validation of gene trap mouse ES cell lines: a test case with the gene Ttrap.
Int J Dev Biol;
53(7): 1045-51, 2009.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19598121
11.
The C20orf133 gene is disrupted in a patient with Kabuki syndrome.
BMJ Case Rep;
20092009.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21720541
12.
Neural crest-specific removal of Zfhx1b in mouse leads to a wide range of neurocristopathies reminiscent of Mowat-Wilson syndrome.
Hum Mol Genet;
16(12): 1423-36, 2007 Jun 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17478475
13.
Smad5 determines murine amnion fate through the control of bone morphogenetic protein expression and signalling levels.
Development;
133(17): 3399-409, 2006 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16887830
14.
Generation of a floxed allele of Smad5 for cre-mediated conditional knockout in the mouse.
Genesis;
37(1): 5-11, 2003 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-14502571
15.
Mice lacking ZFHX1B, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease-mental retardation syndrome.
Am J Hum Genet;
72(2): 465-70, 2003 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-12522767
16.
Slowed conduction and thin myelination of peripheral nerves associated with mutant rho Guanine-nucleotide exchange factor 10.
Am J Hum Genet;
73(4): 926-32, 2003 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-14508709