Detalhe da pesquisa
1.
Caudal Fgfr1 disruption produces localised spinal mis-patterning and a terminal myelocystocele-like phenotype in mice.
Development
; 150(19)2023 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37756583
2.
A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele.
Hum Mol Genet
; 32(17): 2681-2692, 2023 08 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37364051
3.
Genetically engineered multicistronic allele of Pmel yielding highly specific CreERT2-mediated recombination in the melanocyte lineage.
Pigment Cell Melanoma Res
; 36(1): 71-77, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36412082
4.
A Highly Conserved Shh Enhancer Coordinates Hypothalamic and Craniofacial Development.
Front Cell Dev Biol
; 9: 595744, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33869166
5.
Decorin induces rapid secretion of thrombospondin-1 in basal breast carcinoma cells via inhibition of Ras homolog gene family, member A/Rho-associated coiled-coil containing protein kinase 1.
FEBS J
; 280(10): 2353-68, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23350987