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Showing results (1011-1020 of 1,048) with videos related to

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Nature Communications|March 24, 2022
Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolismMahtab 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 StudyMatthew 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 malesJulieta Uthurralt, Heather Gordish-Dressman, Meg Bradbury, et al.
Neurology|July 23, 1998
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patientsE 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 populationsJoseph 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 elementJoseph 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 obesityDavid 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 CasesJaya Punetha, Akanchha Kesari, Prech Uapinyoying, et al.
Genes, Brain, and Behavior|July 1, 2014
GWAS-based pathway analysis differentiates between fluid and crystallized intelligenceA Christoforou, T Espeseth, G Davies, et al.
Frontiers in Immunology|November 12, 2021
Human Complement C4B Allotypes and Deficiencies in Selected Cases With Autoimmune DiseasesDanlei Zhou, Michael Rudnicki, Gilbert T Chua, et al.
Pageof 105

Showing results (1011-1020 of 1,048) with videos related to

Sort By:
Pageof 105
Nature Communications|March 24, 2022
Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolismMahtab 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 StudyMatthew 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 malesJulieta Uthurralt, Heather Gordish-Dressman, Meg Bradbury, et al.
Neurology|July 23, 1998
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patientsE 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 populationsJoseph 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 elementJoseph 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 obesityDavid 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 CasesJaya Punetha, Akanchha Kesari, Prech Uapinyoying, et al.
Genes, Brain, and Behavior|July 1, 2014
GWAS-based pathway analysis differentiates between fluid and crystallized intelligenceA Christoforou, T Espeseth, G Davies, et al.
Frontiers in Immunology|November 12, 2021
Human Complement C4B Allotypes and Deficiencies in Selected Cases With Autoimmune DiseasesDanlei Zhou, Michael Rudnicki, Gilbert T Chua, et al.
Pageof 105