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Nature Communications
|
July 14, 2017
Platelet function is modified by common sequence variation in megakaryocyte super enhancers
Romina Petersen, John J Lambourne, Biola M Javierre, et al.
American Journal of Respiratory and Critical Care Medicine
|
October 30, 2019
Characterization of <i>GDF2</i> Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial Hypertension
Joshua Hodgson, Emilia M Swietlik, Richard M Salmon, et al.
Nature Communications
|
April 14, 2018
Identification of rare sequence variation underlying heritable pulmonary arterial hypertension
Stefan Gräf, Matthias Haimel, Marta Bleda, et al.
Nature
|
June 26, 2020
Whole-genome sequencing of patients with rare diseases in a national health system
Ernest Turro, William J Astle, Karyn Megy, et al.
Cell
|
November 19, 2016
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
William J Astle, Heather Elding, Tao Jiang, et al.
Genome Research
|
September 20, 2011
Assemblathon 1: a competitive assessment of de novo short read assembly methods
Dent Earl, Keith Bradnam, John St John, et al.
Gigascience
|
July 23, 2013
Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate species
Keith R Bradnam, Joseph N Fass, Anton Alexandrov, et al.
The Lancet. Respiratory Medicine
|
December 12, 2018
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis
Christopher J Rhodes, Ken Batai, Marta Bleda, et al.
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Showing results (21-30 of 28) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 28 results.
Nature Communications
|
July 14, 2017
Platelet function is modified by common sequence variation in megakaryocyte super enhancers
Romina Petersen, John J Lambourne, Biola M Javierre, et al.
American Journal of Respiratory and Critical Care Medicine
|
October 30, 2019
Characterization of <i>GDF2</i> Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial Hypertension
Joshua Hodgson, Emilia M Swietlik, Richard M Salmon, et al.
Nature Communications
|
April 14, 2018
Identification of rare sequence variation underlying heritable pulmonary arterial hypertension
Stefan Gräf, Matthias Haimel, Marta Bleda, et al.
Nature
|
June 26, 2020
Whole-genome sequencing of patients with rare diseases in a national health system
Ernest Turro, William J Astle, Karyn Megy, et al.
Cell
|
November 19, 2016
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
William J Astle, Heather Elding, Tao Jiang, et al.
Genome Research
|
September 20, 2011
Assemblathon 1: a competitive assessment of de novo short read assembly methods
Dent Earl, Keith Bradnam, John St John, et al.
Gigascience
|
July 23, 2013
Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate species
Keith R Bradnam, Joseph N Fass, Anton Alexandrov, et al.
The Lancet. Respiratory Medicine
|
December 12, 2018
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis
Christopher J Rhodes, Ken Batai, Marta Bleda, et al.
Page
of 3