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Showing results (951-960 of 1,005) with videos related to

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Journal of the Royal Society of New Zealand|August 4, 2025
Rakeiora Genomics Platform: a pathfinder for genomic medicine research in Aotearoa New ZealandClaire E Rye, Huti Puketapu-Watson, Helen Wihongi, et al.
The New Zealand Medical Journal|August 18, 2018
Genomic medicine must reduce, not compound, health inequities: the case for hauora-enhancing genomic resources for New ZealandStephen P Robertson, Jennie Harre Hindmarsh, Sarah Berry, et al.
JAMA Network Open|January 10, 2022
Factors Associated With Relapse and Treatment of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease in the United KingdomChanjira Satukijchai, Romina Mariano, Silvia Messina, et al.
Cell Reports|August 22, 2019
Suppression of p16 Induces mTORC1-Mediated Nucleotide Metabolic ReprogrammingRaquel Buj, Chi-Wei Chen, Erika S Dahl, et al.
Journal of Community Genetics|June 27, 2026
A primary care pharmacogenetic precision medicine pilot based on specific Māori tribal ethical frameworks and principlesStephen P Robertson, Benjamin J Halliday, Rhonda Tibble, et al.
Science (New York, N.Y.)|June 16, 2022
Spatial centrosome proteome of human neural cells uncovers disease-relevant heterogeneityAdam C O'Neill, Fatma Uzbas, Giulia Antognolli, et al.
Nature Genetics|November 28, 2018
Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regionsPatricia Heyn, Clare V Logan, Adeline Fluteau, et al.
American Journal of Human Genetics|December 25, 2012
Mutations in ECEL1 cause distal arthrogryposis type 5DMargaret J McMillin, Jennifer E Below, Kathryn M Shively, et al.
Nature Communications|November 3, 2021
Extracellular LGALS3BP regulates neural progenitor position and relates to human cortical complexityChristina Kyrousi, Adam C O'Neill, Agnieska Brazovskaja, et al.
American Journal of Human Genetics|May 22, 2012
Cantú syndrome is caused by mutations in ABCC9Bregje W M van Bon, Christian Gilissen, Dorothy K Grange, et al.
Pageof 101

Showing results (951-960 of 1,005) with videos related to

Sort By:
Pageof 101
Journal of the Royal Society of New Zealand|August 4, 2025
Rakeiora Genomics Platform: a pathfinder for genomic medicine research in Aotearoa New ZealandClaire E Rye, Huti Puketapu-Watson, Helen Wihongi, et al.
The New Zealand Medical Journal|August 18, 2018
Genomic medicine must reduce, not compound, health inequities: the case for hauora-enhancing genomic resources for New ZealandStephen P Robertson, Jennie Harre Hindmarsh, Sarah Berry, et al.
JAMA Network Open|January 10, 2022
Factors Associated With Relapse and Treatment of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease in the United KingdomChanjira Satukijchai, Romina Mariano, Silvia Messina, et al.
Cell Reports|August 22, 2019
Suppression of p16 Induces mTORC1-Mediated Nucleotide Metabolic ReprogrammingRaquel Buj, Chi-Wei Chen, Erika S Dahl, et al.
Journal of Community Genetics|June 27, 2026
A primary care pharmacogenetic precision medicine pilot based on specific Māori tribal ethical frameworks and principlesStephen P Robertson, Benjamin J Halliday, Rhonda Tibble, et al.
Science (New York, N.Y.)|June 16, 2022
Spatial centrosome proteome of human neural cells uncovers disease-relevant heterogeneityAdam C O'Neill, Fatma Uzbas, Giulia Antognolli, et al.
Nature Genetics|November 28, 2018
Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regionsPatricia Heyn, Clare V Logan, Adeline Fluteau, et al.
American Journal of Human Genetics|December 25, 2012
Mutations in ECEL1 cause distal arthrogryposis type 5DMargaret J McMillin, Jennifer E Below, Kathryn M Shively, et al.
Nature Communications|November 3, 2021
Extracellular LGALS3BP regulates neural progenitor position and relates to human cortical complexityChristina Kyrousi, Adam C O'Neill, Agnieska Brazovskaja, et al.
American Journal of Human Genetics|May 22, 2012
Cantú syndrome is caused by mutations in ABCC9Bregje W M van Bon, Christian Gilissen, Dorothy K Grange, et al.
Pageof 101