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F Hunter

Showing results (491-500 of 502) with videos related to

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Genome Research|June 5, 2019
Growth disrupting mutations in epigenetic regulatory molecules are associated with abnormalities of epigenetic agingAaron R Jeffries, Reza Maroofian, Claire G Salter, et al.
The Lancet. Global Health|May 13, 2022
City planning policies to support health and sustainability: an international comparison of policy indicators for 25 citiesMelanie Lowe, Deepti Adlakha, James F Sallis, et al.
American Journal of Human Genetics|July 14, 2015
THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual DisabilityRaman Kumar, Mark A Corbett, Bregje W M van Bon, et al.
Wellcome Open Research|March 3, 2023
GroundsWell: Community-engaged and data-informed systems transformation of Urban Green and Blue Space for population health - a new initiativeRuth F Hunter, Sarah E Rodgers, Jeremy Hilton, et al.
The Journal of Clinical Investigation|February 15, 2024
A metabolic signature for NADSYN1-dependent congenital NAD deficiency disorderJustin O Szot, Hartmut Cuny, Ella Mma Martin, et al.
Physics of Plasmas|June 28, 2017
Laser-plasmas in the relativistic-transparency regime: Science and applicationsJuan C Fernández, D Cort Gautier, Chengkung Huang, et al.
Nature Medicine|June 8, 2023
Integrated multi-omics for rapid rare disease diagnosis on a national scaleSebastian Lunke, Sophie E Bouffler, Chirag V Patel, et al.
Nature Human Behaviour|October 20, 2022
A multi-lab test of the facial feedback hypothesis by the Many Smiles CollaborationNicholas A Coles, David S March, Fernando Marmolejo-Ramos, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2024
Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohortKerith-Rae Dias, Rupendra Shrestha, Deborah Schofield, et al.
JAMA|June 24, 2020
Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System, Sebastian Lunke, Stefanie Eggers, et al.
Pageof 51

Showing results (491-500 of 502) with videos related to

Sort By:
Pageof 51
Genome Research|June 5, 2019
Growth disrupting mutations in epigenetic regulatory molecules are associated with abnormalities of epigenetic agingAaron R Jeffries, Reza Maroofian, Claire G Salter, et al.
The Lancet. Global Health|May 13, 2022
City planning policies to support health and sustainability: an international comparison of policy indicators for 25 citiesMelanie Lowe, Deepti Adlakha, James F Sallis, et al.
American Journal of Human Genetics|July 14, 2015
THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual DisabilityRaman Kumar, Mark A Corbett, Bregje W M van Bon, et al.
Wellcome Open Research|March 3, 2023
GroundsWell: Community-engaged and data-informed systems transformation of Urban Green and Blue Space for population health - a new initiativeRuth F Hunter, Sarah E Rodgers, Jeremy Hilton, et al.
The Journal of Clinical Investigation|February 15, 2024
A metabolic signature for NADSYN1-dependent congenital NAD deficiency disorderJustin O Szot, Hartmut Cuny, Ella Mma Martin, et al.
Physics of Plasmas|June 28, 2017
Laser-plasmas in the relativistic-transparency regime: Science and applicationsJuan C Fernández, D Cort Gautier, Chengkung Huang, et al.
Nature Medicine|June 8, 2023
Integrated multi-omics for rapid rare disease diagnosis on a national scaleSebastian Lunke, Sophie E Bouffler, Chirag V Patel, et al.
Nature Human Behaviour|October 20, 2022
A multi-lab test of the facial feedback hypothesis by the Many Smiles CollaborationNicholas A Coles, David S March, Fernando Marmolejo-Ramos, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2024
Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohortKerith-Rae Dias, Rupendra Shrestha, Deborah Schofield, et al.
JAMA|June 24, 2020
Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System, Sebastian Lunke, Stefanie Eggers, et al.
Pageof 51