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Nature Communications
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March 24, 2022
Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolism
Mahtab Tavasoli, Sarah Lahire, Stanislav Sokolenko, et al.
European Journal of Applied Physiology
|
May 22, 2010
A polymorphism near IGF1 is associated with body composition and muscle function in women from the Health, Aging, and Body Composition Study
Matthew C Kostek, Joseph M Devaney, Heather Gordish-Dressman, et al.
BMC Medical Genetics
|
August 21, 2007
PPARalpha L162V underlies variation in serum triglycerides and subcutaneous fat volume in young males
Julieta Uthurralt, Heather Gordish-Dressman, Meg Bradbury, et al.
Neurology
|
July 23, 1998
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients
E Pegoraro, H Marks, C A Garcia, et al.
Pediatric Research
|
February 8, 2011
The 1p13.3 LDL (C)-associated locus shows large effect sizes in young populations
Joseph M Devaney, Paul D Thompson, Paul S Visich, et al.
Journal of Cellular Biochemistry
|
June 4, 2009
Differences in fat and muscle mass associated with a functional human polymorphism in a post-transcriptional BMP2 gene regulatory element
Joseph M Devaney, Laura L Tosi, David T Fritz, et al.
Physiological Genomics
|
August 21, 2014
Multi-omic integrated networks connect DNA methylation and miRNA with skeletal muscle plasticity to chronic exercise in Type 2 diabetic obesity
David S Rowlands, Rachel A Page, William R Sukala, et al.
Journal of Neuromuscular Diseases
|
November 18, 2016
Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 Cases
Jaya Punetha, Akanchha Kesari, Prech Uapinyoying, et al.
Genes, Brain, and Behavior
|
July 1, 2014
GWAS-based pathway analysis differentiates between fluid and crystallized intelligence
A Christoforou, T Espeseth, G Davies, et al.
Frontiers in Immunology
|
November 12, 2021
Human Complement C4B Allotypes and Deficiencies in Selected Cases With Autoimmune Diseases
Danlei Zhou, Michael Rudnicki, Gilbert T Chua, et al.
Page
of 105
Search research articles
Search
Showing results (1011-1020 of 1,048) with videos related to
Sort By:
Page
of 105
Nature Communications
|
March 24, 2022
Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolism
Mahtab Tavasoli, Sarah Lahire, Stanislav Sokolenko, et al.
European Journal of Applied Physiology
|
May 22, 2010
A polymorphism near IGF1 is associated with body composition and muscle function in women from the Health, Aging, and Body Composition Study
Matthew C Kostek, Joseph M Devaney, Heather Gordish-Dressman, et al.
BMC Medical Genetics
|
August 21, 2007
PPARalpha L162V underlies variation in serum triglycerides and subcutaneous fat volume in young males
Julieta Uthurralt, Heather Gordish-Dressman, Meg Bradbury, et al.
Neurology
|
July 23, 1998
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients
E Pegoraro, H Marks, C A Garcia, et al.
Pediatric Research
|
February 8, 2011
The 1p13.3 LDL (C)-associated locus shows large effect sizes in young populations
Joseph M Devaney, Paul D Thompson, Paul S Visich, et al.
Journal of Cellular Biochemistry
|
June 4, 2009
Differences in fat and muscle mass associated with a functional human polymorphism in a post-transcriptional BMP2 gene regulatory element
Joseph M Devaney, Laura L Tosi, David T Fritz, et al.
Physiological Genomics
|
August 21, 2014
Multi-omic integrated networks connect DNA methylation and miRNA with skeletal muscle plasticity to chronic exercise in Type 2 diabetic obesity
David S Rowlands, Rachel A Page, William R Sukala, et al.
Journal of Neuromuscular Diseases
|
November 18, 2016
Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 Cases
Jaya Punetha, Akanchha Kesari, Prech Uapinyoying, et al.
Genes, Brain, and Behavior
|
July 1, 2014
GWAS-based pathway analysis differentiates between fluid and crystallized intelligence
A Christoforou, T Espeseth, G Davies, et al.
Frontiers in Immunology
|
November 12, 2021
Human Complement C4B Allotypes and Deficiencies in Selected Cases With Autoimmune Diseases
Danlei Zhou, Michael Rudnicki, Gilbert T Chua, et al.
Page
of 105