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Tim Morgan

Showing results (31-40 of 45) with videos related to

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Journal of Molecular Medicine (Berlin, Germany)|February 18, 2015
Diverse phenotypic consequences of mutations affecting the C-terminus of FLNAMargriet van Kogelenberg, Alice R Clark, Zandra Jenkins, et al.
Cell Reports|December 6, 2018
A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal MigrationAdam C O'Neill, Christina Kyrousi, Johannes Klaus, et al.
JMIR Mhealth and Uhealth|September 8, 2019
Biofeedback-Assisted Resilience Training for Traumatic and Operational Stress: Preliminary Analysis of a Self-Delivered Digital Health MethodologyPaul N Kizakevich, Randall P Eckhoff, Gregory F Lewis, et al.
American Journal of Human Genetics|October 25, 2011
Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acidKathrin Laue, Hans-Martin Pogoda, Philip B Daniel, et al.
Human Mutation|October 13, 2017
Differential regulation of two FLNA transcripts explains some of the phenotypic heterogeneity in the loss-of-function filaminopathiesZandra A Jenkins, Alison Macharg, Cheng-Yee Chang, et al.
Hypertension (Dallas, Tex. : 1979)|July 2, 2019
Effect of Intensive Blood Pressure Reduction on Left Ventricular Mass, Structure, Function, and Fibrosis in the SPRINT-HEARTBharathi Upadhya, Michael V Rocco, Nicholas M Pajewski, et al.
Human Mutation|December 23, 2011
Disease-associated mutations in the actin-binding domain of filamin B cause cytoplasmic focal accumulations correlating with disease severityPhilip B Daniel, Tim Morgan, Yasemin Alanay, et al.
Brain : a Journal of Neurology|December 18, 2025
A functional role for septin-2 in the maintenance of the axon initial segment and in human cognitive developmentLuisa Weiss, Macarena Pavez, Anastasia Labudina, et al.
Nature Genetics|December 17, 2008
Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesisZandra A Jenkins, Margriet van Kogelenberg, Tim Morgan, et al.
American Journal of Medical Genetics. Part A|November 2, 2011
The male phenotype in osteopathia striata congenita with cranial sclerosisSarah K Holman, Phil Daniel, Zandra A Jenkins, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Journal of Molecular Medicine (Berlin, Germany)|February 18, 2015
Diverse phenotypic consequences of mutations affecting the C-terminus of FLNAMargriet van Kogelenberg, Alice R Clark, Zandra Jenkins, et al.
Cell Reports|December 6, 2018
A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal MigrationAdam C O'Neill, Christina Kyrousi, Johannes Klaus, et al.
JMIR Mhealth and Uhealth|September 8, 2019
Biofeedback-Assisted Resilience Training for Traumatic and Operational Stress: Preliminary Analysis of a Self-Delivered Digital Health MethodologyPaul N Kizakevich, Randall P Eckhoff, Gregory F Lewis, et al.
American Journal of Human Genetics|October 25, 2011
Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acidKathrin Laue, Hans-Martin Pogoda, Philip B Daniel, et al.
Human Mutation|October 13, 2017
Differential regulation of two FLNA transcripts explains some of the phenotypic heterogeneity in the loss-of-function filaminopathiesZandra A Jenkins, Alison Macharg, Cheng-Yee Chang, et al.
Hypertension (Dallas, Tex. : 1979)|July 2, 2019
Effect of Intensive Blood Pressure Reduction on Left Ventricular Mass, Structure, Function, and Fibrosis in the SPRINT-HEARTBharathi Upadhya, Michael V Rocco, Nicholas M Pajewski, et al.
Human Mutation|December 23, 2011
Disease-associated mutations in the actin-binding domain of filamin B cause cytoplasmic focal accumulations correlating with disease severityPhilip B Daniel, Tim Morgan, Yasemin Alanay, et al.
Brain : a Journal of Neurology|December 18, 2025
A functional role for septin-2 in the maintenance of the axon initial segment and in human cognitive developmentLuisa Weiss, Macarena Pavez, Anastasia Labudina, et al.
Nature Genetics|December 17, 2008
Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesisZandra A Jenkins, Margriet van Kogelenberg, Tim Morgan, et al.
American Journal of Medical Genetics. Part A|November 2, 2011
The male phenotype in osteopathia striata congenita with cranial sclerosisSarah K Holman, Phil Daniel, Zandra A Jenkins, et al.
Pageof 5