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Richard Pearson

Showing results (21-30 of 32) with videos related to

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Blood|February 8, 2011
Programming of marginal zone B-cell fate by basic Kruppel-like factor (BKLF/KLF3)Gleb Turchinovich, Thi Thanh Vu, Friederike Frommer, et al.
Systematic Biology|June 13, 2019
The Origins and Diversification of the Exceptionally Rich Gemsnakes (Colubroidea: Lamprophiidae: Pseudoxyrhophiinae) in MadagascarFrank T Burbrink, Sara Ruane, Arianna Kuhn, et al.
Genome Research|August 18, 2016
Indels, structural variation, and recombination drive genomic diversity in Plasmodium falciparumAlistair Miles, Zamin Iqbal, Paul Vauterin, et al.
Plos Genetics|July 23, 2013
ENU-induced mutation in the DNA-binding domain of KLF3 reveals important roles for KLF3 in cardiovascular development and function in miceLois Kelsey, Ann M Flenniken, Dawei Qu, et al.
Human Molecular Genetics|November 8, 2014
Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypesAndrew R Wood, Marcus A Tuke, Mike Nalls, et al.
Scientific Data|February 18, 2025
Compilation of riverine water quality data from the Great Barrier Reef catchment area, northeastern AustraliaCassandra James, Zoe Bainbridge, Stephen Lewis, et al.
Journal of Medical Genetics|March 11, 2020
Pathogenic variants in <i>TNRC6B</i> cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHDJorge Luis Granadillo, Alexander P A Stegmann, Hui Guo, et al.
Nature Genetics|January 8, 2013
Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis, , Michaela Fakiola, et al.
Nature Communications|July 9, 2014
The correlation between reading and mathematics ability at age twelve has a substantial genetic componentOliver S P Davis, Gavin Band, Matti Pirinen, et al.
Biological Psychiatry|July 23, 2013
A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation, , Elvira Bramon, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Blood|February 8, 2011
Programming of marginal zone B-cell fate by basic Kruppel-like factor (BKLF/KLF3)Gleb Turchinovich, Thi Thanh Vu, Friederike Frommer, et al.
Systematic Biology|June 13, 2019
The Origins and Diversification of the Exceptionally Rich Gemsnakes (Colubroidea: Lamprophiidae: Pseudoxyrhophiinae) in MadagascarFrank T Burbrink, Sara Ruane, Arianna Kuhn, et al.
Genome Research|August 18, 2016
Indels, structural variation, and recombination drive genomic diversity in Plasmodium falciparumAlistair Miles, Zamin Iqbal, Paul Vauterin, et al.
Plos Genetics|July 23, 2013
ENU-induced mutation in the DNA-binding domain of KLF3 reveals important roles for KLF3 in cardiovascular development and function in miceLois Kelsey, Ann M Flenniken, Dawei Qu, et al.
Human Molecular Genetics|November 8, 2014
Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypesAndrew R Wood, Marcus A Tuke, Mike Nalls, et al.
Scientific Data|February 18, 2025
Compilation of riverine water quality data from the Great Barrier Reef catchment area, northeastern AustraliaCassandra James, Zoe Bainbridge, Stephen Lewis, et al.
Journal of Medical Genetics|March 11, 2020
Pathogenic variants in <i>TNRC6B</i> cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHDJorge Luis Granadillo, Alexander P A Stegmann, Hui Guo, et al.
Nature Genetics|January 8, 2013
Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis, , Michaela Fakiola, et al.
Nature Communications|July 9, 2014
The correlation between reading and mathematics ability at age twelve has a substantial genetic componentOliver S P Davis, Gavin Band, Matti Pirinen, et al.
Biological Psychiatry|July 23, 2013
A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation, , Elvira Bramon, et al.
Pageof 4