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Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society
|
November 20, 2008
SHOX gene is expressed in vertebral body growth plates in idiopathic and congenital scoliosis: implications for the etiology of scoliosis in Turner syndrome
Gregory Day, Attila Szvetko, Lyn Griffiths, et al.
Genes
|
September 28, 2023
Genetic Characterization of Blood Group Antigens for Polynesian Heritage Norfolk Island Residents
Stacie O'Brien, Rodney A Lea, Sudhir Jadhao, et al.
The Journal of Molecular Diagnostics : JMD
|
August 24, 2019
Variant Call Format-Diagnostic Annotation and Reporting Tool: A Customizable Analysis Pipeline for Identification of Clinically Relevant Genetic Variants in Next-Generation Sequencing Data
Miles C Benton, Robert A Smith, Larisa M Haupt, et al.
Cancer Control : Journal of the Moffitt Cancer Center
|
September 19, 2025
A Preliminary Prospective Study on the Association of Polymorphisms in <i>BDNF</i>, <i>ARRB2</i> and <i>KCNJ6</i> and Response to Fentanyl for Pain Management in Advanced Cancer
John Prenzler, Alison Haywood, Heidi Sutherland G, et al.
Frontiers in Neurology
|
October 2, 2025
Blood pressure lowering for prevention of episodic migraine: results of a pilot randomized, placebo-controlled trial of combination blood pressure lowering medication with propranolol
Cheryl Carcel, Faraidoon Haghdoost, Leo Davies, et al.
Developmental Medicine and Child Neurology
|
January 28, 2016
Eye movement disorders are an early manifestation of CACNA1A mutations in children
Esther M Tantsis, Deepak Gill, Lyn Griffiths, et al.
Genome Biology
|
February 5, 2015
An analysis of DNA methylation in human adipose tissue reveals differential modification of obesity genes before and after gastric bypass and weight loss
Miles C Benton, Alice Johnstone, David Eccles, et al.
Journal of the American College of Cardiology
|
March 10, 2012
Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk
Stefan A Mann, Robyn Otway, Guanglan Guo, et al.
American Journal of Human Genetics
|
August 2, 2007
Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy
Edwin P Kirk, Margaret Sunde, Mauro W Costa, et al.
Annals of Neurology
|
December 23, 2011
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci
Nikolaos A Patsopoulos, , , et al.
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Search research articles
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Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society
|
November 20, 2008
SHOX gene is expressed in vertebral body growth plates in idiopathic and congenital scoliosis: implications for the etiology of scoliosis in Turner syndrome
Gregory Day, Attila Szvetko, Lyn Griffiths, et al.
Genes
|
September 28, 2023
Genetic Characterization of Blood Group Antigens for Polynesian Heritage Norfolk Island Residents
Stacie O'Brien, Rodney A Lea, Sudhir Jadhao, et al.
The Journal of Molecular Diagnostics : JMD
|
August 24, 2019
Variant Call Format-Diagnostic Annotation and Reporting Tool: A Customizable Analysis Pipeline for Identification of Clinically Relevant Genetic Variants in Next-Generation Sequencing Data
Miles C Benton, Robert A Smith, Larisa M Haupt, et al.
Cancer Control : Journal of the Moffitt Cancer Center
|
September 19, 2025
A Preliminary Prospective Study on the Association of Polymorphisms in <i>BDNF</i>, <i>ARRB2</i> and <i>KCNJ6</i> and Response to Fentanyl for Pain Management in Advanced Cancer
John Prenzler, Alison Haywood, Heidi Sutherland G, et al.
Frontiers in Neurology
|
October 2, 2025
Blood pressure lowering for prevention of episodic migraine: results of a pilot randomized, placebo-controlled trial of combination blood pressure lowering medication with propranolol
Cheryl Carcel, Faraidoon Haghdoost, Leo Davies, et al.
Developmental Medicine and Child Neurology
|
January 28, 2016
Eye movement disorders are an early manifestation of CACNA1A mutations in children
Esther M Tantsis, Deepak Gill, Lyn Griffiths, et al.
Genome Biology
|
February 5, 2015
An analysis of DNA methylation in human adipose tissue reveals differential modification of obesity genes before and after gastric bypass and weight loss
Miles C Benton, Alice Johnstone, David Eccles, et al.
Journal of the American College of Cardiology
|
March 10, 2012
Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk
Stefan A Mann, Robyn Otway, Guanglan Guo, et al.
American Journal of Human Genetics
|
August 2, 2007
Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy
Edwin P Kirk, Margaret Sunde, Mauro W Costa, et al.
Annals of Neurology
|
December 23, 2011
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci
Nikolaos A Patsopoulos, , , et al.
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of 4