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BMC Medical Genetics
|
May 21, 2009
Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study
Donna K Arnett, Na Li, Weihong Tang, et al.
The Journal of Molecular Diagnostics : JMD
|
February 25, 2021
Identification of CYP2D6 Haplotypes that Interfere with Commonly Used Assays for Copy Number Variation Characterization
Amy J Turner, Praful Aggarwal, Erin C Boone, et al.
Plos One
|
September 26, 2014
RNA expression profiling of human iPSC-derived cardiomyocytes in a cardiac hypertrophy model
Praful Aggarwal, Amy Turner, Andrea Matter, et al.
The Journal of Molecular Diagnostics : JMD
|
July 20, 2024
Characterization of Reference Materials for DPYD: A GeT-RM Collaborative Project
Andrea Gaedigk, Amy J Turner, Ann M Moyer, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
February 12, 2011
The functional -374T/A polymorphism of the receptor for advanced glycation end products may modulate Crohn's disease
Jan Däbritz, Frauke Friedrichs, Toni Weinhage, et al.
Inflammatory Bowel Diseases
|
June 24, 2005
Comparative phenotypic and CARD15 mutational analysis among African American, Hispanic, and White children with Crohn's disease
Subra Kugathasan, Anthony Loizides, Umesh Babusukumar, et al.
Journal of Personalized Medicine
|
October 27, 2022
Characterization of Novel <i>CYP2D6</i> Alleles across Sub-Saharan African Populations
Wendy Y Wang, David Twesigomwe, Charity Nofziger, et al.
Circulation
|
February 16, 2005
Distinct heritable patterns of angiographic coronary artery disease in families with myocardial infarction
Marcus Fischer, Ulrich Broeckel, Stephan Holmer, et al.
Journal of Hypertension
|
July 14, 2009
Novel genetic variants contributing to left ventricular hypertrophy: the HyperGEN study
Donna K Arnett, Richard B Devereux, Dabeeru C Rao, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2026
Optical Genome Mapping and Long-Read Sequencing Identifies a Novel Dystrophin Gene Inversion in a Patient With Duchenne Muscular Dystrophy
Ryan Gallagher, Alexya Aguilera, Sara Acosta Villarreal, et al.
Page
of 13
Search research articles
Search
Showing results (31-40 of 125) with videos related to
Sort By:
Page
of 13
BMC Medical Genetics
|
May 21, 2009
Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study
Donna K Arnett, Na Li, Weihong Tang, et al.
The Journal of Molecular Diagnostics : JMD
|
February 25, 2021
Identification of CYP2D6 Haplotypes that Interfere with Commonly Used Assays for Copy Number Variation Characterization
Amy J Turner, Praful Aggarwal, Erin C Boone, et al.
Plos One
|
September 26, 2014
RNA expression profiling of human iPSC-derived cardiomyocytes in a cardiac hypertrophy model
Praful Aggarwal, Amy Turner, Andrea Matter, et al.
The Journal of Molecular Diagnostics : JMD
|
July 20, 2024
Characterization of Reference Materials for DPYD: A GeT-RM Collaborative Project
Andrea Gaedigk, Amy J Turner, Ann M Moyer, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
February 12, 2011
The functional -374T/A polymorphism of the receptor for advanced glycation end products may modulate Crohn's disease
Jan Däbritz, Frauke Friedrichs, Toni Weinhage, et al.
Inflammatory Bowel Diseases
|
June 24, 2005
Comparative phenotypic and CARD15 mutational analysis among African American, Hispanic, and White children with Crohn's disease
Subra Kugathasan, Anthony Loizides, Umesh Babusukumar, et al.
Journal of Personalized Medicine
|
October 27, 2022
Characterization of Novel <i>CYP2D6</i> Alleles across Sub-Saharan African Populations
Wendy Y Wang, David Twesigomwe, Charity Nofziger, et al.
Circulation
|
February 16, 2005
Distinct heritable patterns of angiographic coronary artery disease in families with myocardial infarction
Marcus Fischer, Ulrich Broeckel, Stephan Holmer, et al.
Journal of Hypertension
|
July 14, 2009
Novel genetic variants contributing to left ventricular hypertrophy: the HyperGEN study
Donna K Arnett, Richard B Devereux, Dabeeru C Rao, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2026
Optical Genome Mapping and Long-Read Sequencing Identifies a Novel Dystrophin Gene Inversion in a Patient With Duchenne Muscular Dystrophy
Ryan Gallagher, Alexya Aguilera, Sara Acosta Villarreal, et al.
Page
of 13