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Journal of Proteome Research
|
October 7, 2006
Secreted proteome profiling in human RPE cell cultures derived from donors with age related macular degeneration and age matched healthy donors
Eunkyung An, Xiaoning Lu, Jessica Flippin, et al.
Military Medicine
|
September 2, 2015
CK-MM Polymorphism is Associated With Physical Fitness Test Scores in Military Recruits
Courtney Sprouse, Laura L Tosi, Heather Gordish-Dressman, et al.
European Journal of Clinical Investigation
|
February 17, 2015
Circulating and urinary microRNA profile in focal segmental glomerulosclerosis: a pilot study
Ali Ramezani, Joseph M Devaney, Scott Cohen, et al.
Scientific Reports
|
March 7, 2014
Genomics in premature infants: a non-invasive strategy to obtain high-quality DNA
Mariam Said, Clint Cappiello, Joseph M Devaney, et al.
Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research
|
May 23, 2012
Genetic influences on vitamin D status and forearm fracture risk in African American children
Leticia Manning Ryan, James M Chamberlain, Steven A Singer, et al.
Scientific Reports
|
December 17, 2015
Are Immune Modulating Single Nucleotide Polymorphisms Associated with Necrotizing Enterocolitis?
Ashanti L Franklin, Mariam Said, Clint D Cappiello, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
March 27, 2010
CCL2 and CCR2 polymorphisms are associated with markers of exercise-induced skeletal muscle damage
Monica J Hubal, Joseph M Devaney, Eric P Hoffman, et al.
Medicine and Science in Sports and Exercise
|
July 6, 2004
Functional polymorphisms associated with human muscle size and strength
Paul D Thompson, Niall Moyna, Richard Seip, et al.
American Heart Journal
|
July 31, 2013
Racial disparity with on-treatment platelet reactivity in patients undergoing percutaneous coronary intervention
Lakshmana K Pendyala, Rebecca Torguson, Joshua P Loh, et al.
American Journal of Human Genetics
|
April 10, 2002
Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia
Eri Arikawa-Hirasawa, Alexander H Le, Ichizo Nishino, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 71) with videos related to
Sort By:
Page
of 8
Journal of Proteome Research
|
October 7, 2006
Secreted proteome profiling in human RPE cell cultures derived from donors with age related macular degeneration and age matched healthy donors
Eunkyung An, Xiaoning Lu, Jessica Flippin, et al.
Military Medicine
|
September 2, 2015
CK-MM Polymorphism is Associated With Physical Fitness Test Scores in Military Recruits
Courtney Sprouse, Laura L Tosi, Heather Gordish-Dressman, et al.
European Journal of Clinical Investigation
|
February 17, 2015
Circulating and urinary microRNA profile in focal segmental glomerulosclerosis: a pilot study
Ali Ramezani, Joseph M Devaney, Scott Cohen, et al.
Scientific Reports
|
March 7, 2014
Genomics in premature infants: a non-invasive strategy to obtain high-quality DNA
Mariam Said, Clint Cappiello, Joseph M Devaney, et al.
Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research
|
May 23, 2012
Genetic influences on vitamin D status and forearm fracture risk in African American children
Leticia Manning Ryan, James M Chamberlain, Steven A Singer, et al.
Scientific Reports
|
December 17, 2015
Are Immune Modulating Single Nucleotide Polymorphisms Associated with Necrotizing Enterocolitis?
Ashanti L Franklin, Mariam Said, Clint D Cappiello, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
March 27, 2010
CCL2 and CCR2 polymorphisms are associated with markers of exercise-induced skeletal muscle damage
Monica J Hubal, Joseph M Devaney, Eric P Hoffman, et al.
Medicine and Science in Sports and Exercise
|
July 6, 2004
Functional polymorphisms associated with human muscle size and strength
Paul D Thompson, Niall Moyna, Richard Seip, et al.
American Heart Journal
|
July 31, 2013
Racial disparity with on-treatment platelet reactivity in patients undergoing percutaneous coronary intervention
Lakshmana K Pendyala, Rebecca Torguson, Joshua P Loh, et al.
American Journal of Human Genetics
|
April 10, 2002
Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia
Eri Arikawa-Hirasawa, Alexander H Le, Ichizo Nishino, et al.
Page
of 8