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William E Tidyman

Showing results (1-10 of 20) with videos related to

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Current Genetic Medicine Reports|December 13, 2016
Expansion of the RASopathiesWilliam E Tidyman, Katherine A Rauen
Methods in Molecular Biology (Clifton, N.J.)|September 3, 2010
Mutational and functional analysis in human Ras/MAP kinase genetic syndromesWilliam E Tidyman, Katherine A Rauen
Expert Reviews in Molecular Medicine|December 10, 2008
Noonan, Costello and cardio-facio-cutaneous syndromes: dysregulation of the Ras-MAPK pathwayWilliam E Tidyman, Katherine A Rauen
Human Molecular Genetics|July 15, 2016
Pathogenetics of the RASopathiesWilliam E Tidyman, Katherine A Rauen
Current Opinion in Genetics & Development|May 27, 2009
The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulationWilliam E Tidyman, Katherine A Rauen
Disease Models & Mechanisms|June 7, 2024
RASopathies - what they reveal about RAS/MAPK signaling in skeletal muscle developmentKatherine A Rauen, William E Tidyman
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 16, 2011
Skeletal muscle pathology in Costello and cardio-facio-cutaneous syndromes: developmental consequences of germline Ras/MAPK activation on myogenesisWilliam E Tidyman, Han S Lee, Katherine A Rauen
American Journal of Medical Genetics. Part A|December 4, 2020
Familial cardio-facio-cutaneous syndrome: Vertical transmission of the BRAF p.G464R pathogenic variant and review of the literatureKatherine A Rauen, Yoshiko Maeda, Alena Egense, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|February 1, 2021
Ras/MAPK dysregulation in development causes a skeletal myopathy in an activating Braf<sup>L597V</sup> mouse model for cardio-facio-cutaneous syndromeYoshiko Maeda, William E Tidyman, Bradley P Ander, et al.
Disease Models & Mechanisms|September 23, 2021
MEK-inhibitor-mediated rescue of skeletal myopathy caused by activating Hras mutation in a Costello syndrome mouse modelWilliam E Tidyman, Alice F Goodwin, Yoshiko Maeda, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Current Genetic Medicine Reports|December 13, 2016
Expansion of the RASopathiesWilliam E Tidyman, Katherine A Rauen
Methods in Molecular Biology (Clifton, N.J.)|September 3, 2010
Mutational and functional analysis in human Ras/MAP kinase genetic syndromesWilliam E Tidyman, Katherine A Rauen
Expert Reviews in Molecular Medicine|December 10, 2008
Noonan, Costello and cardio-facio-cutaneous syndromes: dysregulation of the Ras-MAPK pathwayWilliam E Tidyman, Katherine A Rauen
Human Molecular Genetics|July 15, 2016
Pathogenetics of the RASopathiesWilliam E Tidyman, Katherine A Rauen
Current Opinion in Genetics & Development|May 27, 2009
The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulationWilliam E Tidyman, Katherine A Rauen
Disease Models & Mechanisms|June 7, 2024
RASopathies - what they reveal about RAS/MAPK signaling in skeletal muscle developmentKatherine A Rauen, William E Tidyman
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 16, 2011
Skeletal muscle pathology in Costello and cardio-facio-cutaneous syndromes: developmental consequences of germline Ras/MAPK activation on myogenesisWilliam E Tidyman, Han S Lee, Katherine A Rauen
American Journal of Medical Genetics. Part A|December 4, 2020
Familial cardio-facio-cutaneous syndrome: Vertical transmission of the BRAF p.G464R pathogenic variant and review of the literatureKatherine A Rauen, Yoshiko Maeda, Alena Egense, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|February 1, 2021
Ras/MAPK dysregulation in development causes a skeletal myopathy in an activating Braf<sup>L597V</sup> mouse model for cardio-facio-cutaneous syndromeYoshiko Maeda, William E Tidyman, Bradley P Ander, et al.
Disease Models & Mechanisms|September 23, 2021
MEK-inhibitor-mediated rescue of skeletal myopathy caused by activating Hras mutation in a Costello syndrome mouse modelWilliam E Tidyman, Alice F Goodwin, Yoshiko Maeda, et al.
Pageof 2