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Showing results (1211-1220 of 1,248) with videos related to
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Brain : a Journal of Neurology
|
May 8, 2007
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies
Haiyan Zhou, Heinz Jungbluth, Caroline A Sewry, et al.
Ophthalmology
|
January 22, 2026
LASIK for Hyperopia: A Report by the American Academy of Ophthalmology
Marcony R Santhiago, W Allan Steigleman, Zaina N Al-Mohtaseb, et al.
Neuromuscular Disorders : NMD
|
January 19, 2010
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Haiyan Zhou, Suzanne Lillis, Ryan E Loy, et al.
International Journal of Cancer
|
May 27, 2010
Use of cyclin D1 in conjunction with human papillomavirus status to predict outcome in oropharyngeal cancer
Angela M Hong, Timothy A Dobbins, Cheok S Lee, et al.
Physiological and Biochemical Zoology : PBZ
|
October 12, 2019
Genomics of Early Cardiac Dysfunction and Mortality in Obese <i>Drosophila melanogaster</i>
James N Kezos, Mark A Phillips, Misty D Thomas, et al.
ACS Chemical Biology
|
May 21, 2013
Selective small molecule probes for the hypoxia inducible factor (HIF) prolyl hydroxylases
Rasheduzzaman Chowdhury, José Ignacio Candela-Lena, Mun Chiang Chan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 19, 2018
Metal-free class Ie ribonucleotide reductase from pathogens initiates catalysis with a tyrosine-derived dihydroxyphenylalanine radical
Elizabeth J Blaesi, Gavin M Palowitch, Kai Hu, et al.
EMBO Reports
|
April 5, 2011
The oncometabolite 2-hydroxyglutarate inhibits histone lysine demethylases
Rasheduzzaman Chowdhury, Kar Kheng Yeoh, Ya-Min Tian, et al.
American Journal of Human Genetics
|
March 15, 2022
Familial long-read sequencing increases yield of de novo mutations
Michelle D Noyes, William T Harvey, David Porubsky, et al.
Cancer Research
|
August 15, 2008
Inhibition of the sodium/potassium ATPase impairs N-glycan expression and function
Reza Beheshti Zavareh, Ken S Lau, Rose Hurren, et al.
Page
of 125
Search research articles
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Showing results (1211-1220 of 1,248) with videos related to
Sort By:
Page
of 125
Brain : a Journal of Neurology
|
May 8, 2007
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies
Haiyan Zhou, Heinz Jungbluth, Caroline A Sewry, et al.
Ophthalmology
|
January 22, 2026
LASIK for Hyperopia: A Report by the American Academy of Ophthalmology
Marcony R Santhiago, W Allan Steigleman, Zaina N Al-Mohtaseb, et al.
Neuromuscular Disorders : NMD
|
January 19, 2010
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Haiyan Zhou, Suzanne Lillis, Ryan E Loy, et al.
International Journal of Cancer
|
May 27, 2010
Use of cyclin D1 in conjunction with human papillomavirus status to predict outcome in oropharyngeal cancer
Angela M Hong, Timothy A Dobbins, Cheok S Lee, et al.
Physiological and Biochemical Zoology : PBZ
|
October 12, 2019
Genomics of Early Cardiac Dysfunction and Mortality in Obese <i>Drosophila melanogaster</i>
James N Kezos, Mark A Phillips, Misty D Thomas, et al.
ACS Chemical Biology
|
May 21, 2013
Selective small molecule probes for the hypoxia inducible factor (HIF) prolyl hydroxylases
Rasheduzzaman Chowdhury, José Ignacio Candela-Lena, Mun Chiang Chan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 19, 2018
Metal-free class Ie ribonucleotide reductase from pathogens initiates catalysis with a tyrosine-derived dihydroxyphenylalanine radical
Elizabeth J Blaesi, Gavin M Palowitch, Kai Hu, et al.
EMBO Reports
|
April 5, 2011
The oncometabolite 2-hydroxyglutarate inhibits histone lysine demethylases
Rasheduzzaman Chowdhury, Kar Kheng Yeoh, Ya-Min Tian, et al.
American Journal of Human Genetics
|
March 15, 2022
Familial long-read sequencing increases yield of de novo mutations
Michelle D Noyes, William T Harvey, David Porubsky, et al.
Cancer Research
|
August 15, 2008
Inhibition of the sodium/potassium ATPase impairs N-glycan expression and function
Reza Beheshti Zavareh, Ken S Lau, Rose Hurren, et al.
Page
of 125