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When you enter multiple keywords separated by space, your search will contain results that match any of the keywords (OR search).
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3 Hits
Search Condition : Filter (MeSH = Craniofacial Abnormalities / genetics)
Species
Resource
Link
Mice
Emx1-Cre KI delta neo(RBRC01345)
34774
De novo inbred heterozygous Zeb2/Sip1 mutant mice uniquely generated by germ-line conditional knockout exhibit craniofacial, callosal and behavioral defects associated with Mowat-Wilson syndrome.
Hum. Mol. Genet.
2015-11-15
Pubmed
Full text
Human and Animal Cells
6560
Trps1 plays a pivotal role downstream of Gdf5 signaling in promoting chondrogenesis and apoptosis of ATDC5 cells.
Genes Cells
2008-4
Pubmed
Full text
Zebrafish
T2KSAG?
5586
Expression of H-RASV12 in a zebrafish model of Costello syndrome causes cellular senescence in adult proliferating cells.
Dis Model Mech
2009-1
Pubmed
Full text
