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Biophysical Journal
|
March 27, 2015
LKB1/Mo25/STRAD uniquely impacts sarcomeric contractile function and posttranslational modification
Samantha 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 mice
Camille 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 variants
Adrienne 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 fibrosis
Melissa 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 variation
Camille L Birch, Brandon M Wilk, Manavalan Gajapathy, et al.
BMC Bioinformatics
|
October 17, 2019
VarSight: prioritizing clinically reported variants with binary classification algorithms
James M Holt, Brandon Wilk, Camille L Birch, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Biophysical Journal
|
March 27, 2015
LKB1/Mo25/STRAD uniquely impacts sarcomeric contractile function and posttranslational modification
Samantha 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 mice
Camille 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 variants
Adrienne 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 fibrosis
Melissa 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 variation
Camille L Birch, Brandon M Wilk, Manavalan Gajapathy, et al.
BMC Bioinformatics
|
October 17, 2019
VarSight: prioritizing clinically reported variants with binary classification algorithms
James M Holt, Brandon Wilk, Camille L Birch, et al.
Page
of 1