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Communications Medicine
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May 19, 2025
Interpretable machine learning leverages proteomics to improve cardiovascular disease risk prediction and biomarker identification
Héctor Climente-González, Min Oh, Urszula Chajewska, et al.
Neurology
|
January 20, 2019
Genetic variation in <i>PLEKHG1</i> is associated with white matter hyperintensities (n = 11,226)
Matthew Traylor, Daniel J Tozer, Iain D Croall, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
May 13, 2018
Protein Engineering on Human Recombinant Follistatin: Enhancing Pharmacokinetic Characteristics for Therapeutic Application
Chuan Shen, Andrea Iskenderian, Dianna Lundberg, et al.
Atherosclerosis
|
April 1, 2014
Association of the novel single-nucleotide polymorphism which increases oxidized low-density lipoprotein levels with cerebrovascular disease events
Kari-Matti Mäkelä, Matthew Traylor, Niku Oksala, et al.
Iscience
|
November 10, 2025
Mapping atherogenesis mechanisms in smooth muscle cells by targeting genes linked to coronary artery disease
Julián Albarrán-Juárez, Anton Markov, Anne Louise Jensen, et al.
Stroke
|
January 1, 2015
Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke
Poneh Adib-Samii, William Devan, Matthew Traylor, et al.
Nature Communications
|
October 17, 2022
Systematic Mendelian randomization using the human plasma proteome to discover potential therapeutic targets for stroke
Lingyan Chen, James E Peters, Bram Prins, et al.
Plos One
|
October 10, 2019
Genetic associations with radiological damage in rheumatoid arthritis: Meta-analysis of seven genome-wide association studies of 2,775 cases
Matthew Traylor, Rachel Knevel, Jing Cui, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 11, 2023
Profiling the genome and proteome of metabolic dysfunction-associated steatotic liver disease identifies potential therapeutic targets
Jun Liu, Sile Hu, Lingyan Chen, et al.
Circulation. Genomic and Precision Medicine
|
July 16, 2019
Subtype Specificity of Genetic Loci Associated With Stroke in 16 664 Cases and 32 792 Controls
Matthew Traylor, Christopher D Anderson, Loes C A Rutten-Jacobs, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 97) with videos related to
Sort By:
Page
of 10
Communications Medicine
|
May 19, 2025
Interpretable machine learning leverages proteomics to improve cardiovascular disease risk prediction and biomarker identification
Héctor Climente-González, Min Oh, Urszula Chajewska, et al.
Neurology
|
January 20, 2019
Genetic variation in <i>PLEKHG1</i> is associated with white matter hyperintensities (n = 11,226)
Matthew Traylor, Daniel J Tozer, Iain D Croall, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
May 13, 2018
Protein Engineering on Human Recombinant Follistatin: Enhancing Pharmacokinetic Characteristics for Therapeutic Application
Chuan Shen, Andrea Iskenderian, Dianna Lundberg, et al.
Atherosclerosis
|
April 1, 2014
Association of the novel single-nucleotide polymorphism which increases oxidized low-density lipoprotein levels with cerebrovascular disease events
Kari-Matti Mäkelä, Matthew Traylor, Niku Oksala, et al.
Iscience
|
November 10, 2025
Mapping atherogenesis mechanisms in smooth muscle cells by targeting genes linked to coronary artery disease
Julián Albarrán-Juárez, Anton Markov, Anne Louise Jensen, et al.
Stroke
|
January 1, 2015
Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke
Poneh Adib-Samii, William Devan, Matthew Traylor, et al.
Nature Communications
|
October 17, 2022
Systematic Mendelian randomization using the human plasma proteome to discover potential therapeutic targets for stroke
Lingyan Chen, James E Peters, Bram Prins, et al.
Plos One
|
October 10, 2019
Genetic associations with radiological damage in rheumatoid arthritis: Meta-analysis of seven genome-wide association studies of 2,775 cases
Matthew Traylor, Rachel Knevel, Jing Cui, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 11, 2023
Profiling the genome and proteome of metabolic dysfunction-associated steatotic liver disease identifies potential therapeutic targets
Jun Liu, Sile Hu, Lingyan Chen, et al.
Circulation. Genomic and Precision Medicine
|
July 16, 2019
Subtype Specificity of Genetic Loci Associated With Stroke in 16 664 Cases and 32 792 Controls
Matthew Traylor, Christopher D Anderson, Loes C A Rutten-Jacobs, et al.
Page
of 10