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Camille L Birch

Showing results (1-10 of 6) with videos related to

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Biophysical Journal|March 27, 2015
LKB1/Mo25/STRAD uniquely impacts sarcomeric contractile function and posttranslational modificationSamantha M Behunin, Marissa A Lopez-Pier, Camille L Birch, et al.
American Journal of Physiology. Heart and Circulatory Physiology|May 21, 2016
Sex dimorphisms of crossbridge cycling kinetics in transgenic hypertrophic cardiomyopathy miceCamille L Birch, Samantha M Behunin, Marissa A Lopez-Pier, et al.
Human Mutation|May 11, 2022
DOCKopathies: A systematic review of the clinical pathologies associated with human DOCK pathogenic variantsAdrienne Samani, Katherine G English, Michael A Lopez, et al.
Cold Spring Harbor Molecular Case Studies|February 5, 2020
Applying whole-genome sequencing in relation to phenotype and outcomes in siblings with cystic fibrosisMelissa A Wilk, Andrew T Braun, Philip M Farrell, et al.
Journal of Translational Medicine|December 24, 2025
Uncovering the genetic architecture of ME/CFS: a precision approach reveals impact of rare monogenic variationCamille L Birch, Brandon M Wilk, Manavalan Gajapathy, et al.
BMC Bioinformatics|October 17, 2019
VarSight: prioritizing clinically reported variants with binary classification algorithmsJames M Holt, Brandon Wilk, Camille L Birch, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Biophysical Journal|March 27, 2015
LKB1/Mo25/STRAD uniquely impacts sarcomeric contractile function and posttranslational modificationSamantha M Behunin, Marissa A Lopez-Pier, Camille L Birch, et al.
American Journal of Physiology. Heart and Circulatory Physiology|May 21, 2016
Sex dimorphisms of crossbridge cycling kinetics in transgenic hypertrophic cardiomyopathy miceCamille L Birch, Samantha M Behunin, Marissa A Lopez-Pier, et al.
Human Mutation|May 11, 2022
DOCKopathies: A systematic review of the clinical pathologies associated with human DOCK pathogenic variantsAdrienne Samani, Katherine G English, Michael A Lopez, et al.
Cold Spring Harbor Molecular Case Studies|February 5, 2020
Applying whole-genome sequencing in relation to phenotype and outcomes in siblings with cystic fibrosisMelissa A Wilk, Andrew T Braun, Philip M Farrell, et al.
Journal of Translational Medicine|December 24, 2025
Uncovering the genetic architecture of ME/CFS: a precision approach reveals impact of rare monogenic variationCamille L Birch, Brandon M Wilk, Manavalan Gajapathy, et al.
BMC Bioinformatics|October 17, 2019
VarSight: prioritizing clinically reported variants with binary classification algorithmsJames M Holt, Brandon Wilk, Camille L Birch, et al.
Pageof 1