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Zoe Crane-Smith

Showing results (1-10 of 5) with videos related to

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The FEBS Journal|January 29, 2013
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 1Thomas Neill, Holly R Jones, Zoe Crane-Smith, et al.
Development (Cambridge, England)|September 27, 2023
Caudal Fgfr1 disruption produces localised spinal mis-patterning and a terminal myelocystocele-like phenotype in miceEirini Maniou, Faduma Farah, Abigail R Marshall, et al.
Frontiers in Cell and Developmental Biology|April 19, 2021
A Highly Conserved <i>Shh</i> Enhancer Coordinates Hypothalamic and Craniofacial DevelopmentZoe Crane-Smith, Jeffrey Schoenebeck, Katy A Graham, et al.
Pigment Cell & Melanoma Research|November 22, 2022
Genetically engineered multicistronic allele of Pmel yielding highly specific CreERT2-mediated recombination in the melanocyte lineageEmma L Wilkinson, Louise C Brennan, Olivia J Harrison, et al.
Human Molecular Genetics|June 26, 2023
A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephaloceleZoe Crane-Smith, Sandra C P De Castro, Evanthia Nikolopoulou, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
The FEBS Journal|January 29, 2013
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 1Thomas Neill, Holly R Jones, Zoe Crane-Smith, et al.
Development (Cambridge, England)|September 27, 2023
Caudal Fgfr1 disruption produces localised spinal mis-patterning and a terminal myelocystocele-like phenotype in miceEirini Maniou, Faduma Farah, Abigail R Marshall, et al.
Frontiers in Cell and Developmental Biology|April 19, 2021
A Highly Conserved <i>Shh</i> Enhancer Coordinates Hypothalamic and Craniofacial DevelopmentZoe Crane-Smith, Jeffrey Schoenebeck, Katy A Graham, et al.
Pigment Cell & Melanoma Research|November 22, 2022
Genetically engineered multicistronic allele of Pmel yielding highly specific CreERT2-mediated recombination in the melanocyte lineageEmma L Wilkinson, Louise C Brennan, Olivia J Harrison, et al.
Human Molecular Genetics|June 26, 2023
A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephaloceleZoe Crane-Smith, Sandra C P De Castro, Evanthia Nikolopoulou, et al.
Pageof 1