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Journal of the Royal Society, Interface
|
July 20, 2018
Greater wealth inequality, less polygyny: rethinking the polygyny threshold model
Cody T Ross, Monique Borgerhoff Mulder, Seung-Yun Oh, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 16, 1999
Orally bioavailable nonpeptide vitronectin receptor antagonists with efficacy in an osteoporosis model
W H Miller, W E Bondinell, R D Cousins, et al.
Circulation. Heart Failure
|
January 5, 2024
Protocolized Natriuresis-Guided Decongestion Improves Diuretic Response: The Multicenter ENACT-HF Study
Jeroen Dauw, Kristina Charaya, Małgorzata Lelonek, et al.
ESC Heart Failure
|
October 28, 2021
Rationale and Design of the Efficacy of a Standardized Diuretic Protocol in Acute Heart Failure Study
Jeroen Dauw, Malgorzata Lelonek, Isabel Zegri-Reiriz, et al.
Journal of Medicinal Chemistry
|
November 2, 2022
Discovery of Ervogastat (PF-06865571): A Potent and Selective Inhibitor of Diacylglycerol Acyltransferase 2 for the Treatment of Non-alcoholic Steatohepatitis
Kentaro Futatsugi, Shawn Cabral, Daniel W Kung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 2, 2018
Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project
Pauline Robbe, Niko Popitsch, Samantha J L Knight, et al.
Science (New York, N.Y.)
|
May 29, 2025
Predicting expression-altering promoter mutations with deep learning
Kishore Jaganathan, Nicole Ersaro, Gherman Novakovsky, et al.
Genomics
|
February 6, 2002
Physical and transcript map of the hereditary prostate cancer region at xq27
Dietrich A Stephan, Gareth R Howell, Tanya M Teslovich, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 3, 2026
Blood-based RNA-Seq of 5412 individuals with rare disease identifies new candidate diagnoses in the National Genomic Research Library
Jenny Lord, Alistair T Pagnamenta, Letizia Vestito, et al.
Nature Communications
|
May 19, 2026
High-depth whole genome sequencing of premalignant breast lesions reveals rearrangement hotspots and personalized management opportunities
Lucia Chmelova, Helen R Davies, Andrea Degasperi, et al.
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of 93
Search research articles
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Showing results (891-900 of 927) with videos related to
Sort By:
Page
of 93
Journal of the Royal Society, Interface
|
July 20, 2018
Greater wealth inequality, less polygyny: rethinking the polygyny threshold model
Cody T Ross, Monique Borgerhoff Mulder, Seung-Yun Oh, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 16, 1999
Orally bioavailable nonpeptide vitronectin receptor antagonists with efficacy in an osteoporosis model
W H Miller, W E Bondinell, R D Cousins, et al.
Circulation. Heart Failure
|
January 5, 2024
Protocolized Natriuresis-Guided Decongestion Improves Diuretic Response: The Multicenter ENACT-HF Study
Jeroen Dauw, Kristina Charaya, Małgorzata Lelonek, et al.
ESC Heart Failure
|
October 28, 2021
Rationale and Design of the Efficacy of a Standardized Diuretic Protocol in Acute Heart Failure Study
Jeroen Dauw, Malgorzata Lelonek, Isabel Zegri-Reiriz, et al.
Journal of Medicinal Chemistry
|
November 2, 2022
Discovery of Ervogastat (PF-06865571): A Potent and Selective Inhibitor of Diacylglycerol Acyltransferase 2 for the Treatment of Non-alcoholic Steatohepatitis
Kentaro Futatsugi, Shawn Cabral, Daniel W Kung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 2, 2018
Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project
Pauline Robbe, Niko Popitsch, Samantha J L Knight, et al.
Science (New York, N.Y.)
|
May 29, 2025
Predicting expression-altering promoter mutations with deep learning
Kishore Jaganathan, Nicole Ersaro, Gherman Novakovsky, et al.
Genomics
|
February 6, 2002
Physical and transcript map of the hereditary prostate cancer region at xq27
Dietrich A Stephan, Gareth R Howell, Tanya M Teslovich, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 3, 2026
Blood-based RNA-Seq of 5412 individuals with rare disease identifies new candidate diagnoses in the National Genomic Research Library
Jenny Lord, Alistair T Pagnamenta, Letizia Vestito, et al.
Nature Communications
|
May 19, 2026
High-depth whole genome sequencing of premalignant breast lesions reveals rearrangement hotspots and personalized management opportunities
Lucia Chmelova, Helen R Davies, Andrea Degasperi, et al.
Page
of 93