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Katherine Fu

Showing results (11-20 of 36) with videos related to

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Disease Models & Mechanisms|July 5, 2024
Craniofacial studies in chicken embryos confirm the pathogenicity of human FZD2 variants associated with Robinow syndromeShruti S Tophkhane, Katherine Fu, Esther M Verheyen, et al.
Cells, Tissues, Organs|November 6, 2010
Spatiotemporal localization of periostin and its potential role in epithelial-mesenchymal transition during palatal fusionYukiko Kitase, Keisuke Yamashiro, Katherine Fu, et al.
Developmental Biology|November 9, 2004
A new origin for the maxillary jawSang-Hwy Lee, Olivier Bédard, Marcela Buchtová, et al.
Research in Engineering Design|September 6, 2022
Comparing the effect of virtual and in-person instruction on students' performance in a design for additive manufacturing learning activityAnastasia M K Schauer, Kenton B Fillingim, Anna Pavleszek, et al.
Zoology (Jena, Germany)|May 15, 2007
Embryonic development of Python sebae - II: Craniofacial microscopic anatomy, cell proliferation and apoptosisMarcela Buchtová, Julia C Boughner, Katherine Fu, et al.
Zoology (Jena, Germany)|May 15, 2007
Embryonic development of Python sebae - I: Staging criteria and macroscopic skeletal morphogenesis of the head and limbsJulia C Boughner, Marcela Buchtová, Katherine Fu, et al.
Neurology. Education|August 14, 2025
Education Research: The Effect of an X + Y Schedule Model on Neurology Residency TrainingShuvro Roy, Katherine Fu, Timothy E Ryan, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|August 2, 2011
Development of high-concentration lipoplexes for in vivo gene function studies in vertebrate embryosPoongodi Geetha-Loganathan, Suresh Nimmagadda, Ismail Hafez, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|March 12, 2013
Dual functions for WNT5A during cartilage development and in diseaseSara Hosseini-Farahabadi, Poongodi Geetha-Loganathan, Katherine Fu, et al.
Human Molecular Genetics|April 30, 2019
Robinow syndrome skeletal phenotypes caused by the WNT5AC83S variant are due to dominant interference with chondrogenesisSarah J Gignac, Sara Hosseini-Farahabadi, Takashi Akazawa, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Disease Models & Mechanisms|July 5, 2024
Craniofacial studies in chicken embryos confirm the pathogenicity of human FZD2 variants associated with Robinow syndromeShruti S Tophkhane, Katherine Fu, Esther M Verheyen, et al.
Cells, Tissues, Organs|November 6, 2010
Spatiotemporal localization of periostin and its potential role in epithelial-mesenchymal transition during palatal fusionYukiko Kitase, Keisuke Yamashiro, Katherine Fu, et al.
Developmental Biology|November 9, 2004
A new origin for the maxillary jawSang-Hwy Lee, Olivier Bédard, Marcela Buchtová, et al.
Research in Engineering Design|September 6, 2022
Comparing the effect of virtual and in-person instruction on students' performance in a design for additive manufacturing learning activityAnastasia M K Schauer, Kenton B Fillingim, Anna Pavleszek, et al.
Zoology (Jena, Germany)|May 15, 2007
Embryonic development of Python sebae - II: Craniofacial microscopic anatomy, cell proliferation and apoptosisMarcela Buchtová, Julia C Boughner, Katherine Fu, et al.
Zoology (Jena, Germany)|May 15, 2007
Embryonic development of Python sebae - I: Staging criteria and macroscopic skeletal morphogenesis of the head and limbsJulia C Boughner, Marcela Buchtová, Katherine Fu, et al.
Neurology. Education|August 14, 2025
Education Research: The Effect of an X + Y Schedule Model on Neurology Residency TrainingShuvro Roy, Katherine Fu, Timothy E Ryan, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|August 2, 2011
Development of high-concentration lipoplexes for in vivo gene function studies in vertebrate embryosPoongodi Geetha-Loganathan, Suresh Nimmagadda, Ismail Hafez, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|March 12, 2013
Dual functions for WNT5A during cartilage development and in diseaseSara Hosseini-Farahabadi, Poongodi Geetha-Loganathan, Katherine Fu, et al.
Human Molecular Genetics|April 30, 2019
Robinow syndrome skeletal phenotypes caused by the WNT5AC83S variant are due to dominant interference with chondrogenesisSarah J Gignac, Sara Hosseini-Farahabadi, Takashi Akazawa, et al.
Pageof 4