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Showing results (661-670 of 677) with videos related to

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Nature Communications|May 4, 2021
DNMT1 reads heterochromatic H4K20me3 to reinforce LINE-1 DNA methylationWendan Ren, Huitao Fan, Sara A Grimm, et al.
Science Advances|April 16, 2025
In situ crystallographic mapping constrains sulfate precipitation and timing in Jezero crater, MarsMichael W M Jones, David T Flannery, Joel A Hurowitz, et al.
Nature|May 13, 2021
An aged immune system drives senescence and ageing of solid organsMatthew J Yousefzadeh, Rafael R Flores, Yi Zhu, et al.
Science Advances|July 2, 2025
In situ evidence for serpentinization within the Máaz formation, Jezero crater, MarsNicholas J Tosca, Michael M Tice, Joel A Hurowitz, et al.
Global Health, Epidemiology and Genomics|December 26, 2017
H3Africa AWI-Gen Collaborative Centre: a resource to study the interplay between genomic and environmental risk factors for cardiometabolic diseases in four sub-Saharan African countriesM Ramsay, N Crowther, E Tambo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 18, 2019
Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basisKarin Weiss, Hayley P Lazar, Alina Kurolap, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 8, 2019
The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basisKarin Weiss, Hayley P Lazar, Alina Kurolap, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaborationDuncan S Palmer, Barney Hill, Sam Hodgson, et al.
Science (New York, N.Y.)|August 25, 2022
An olivine cumulate outcrop on the floor of Jezero crater, MarsY Liu, M M Tice, M E Schmidt, et al.
Nature Communications|February 17, 2019
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and languageLot Snijders Blok, Justine Rousseau, Joanna Twist, et al.
Pageof 68

Showing results (661-670 of 677) with videos related to

Sort By:
Pageof 68
Nature Communications|May 4, 2021
DNMT1 reads heterochromatic H4K20me3 to reinforce LINE-1 DNA methylationWendan Ren, Huitao Fan, Sara A Grimm, et al.
Science Advances|April 16, 2025
In situ crystallographic mapping constrains sulfate precipitation and timing in Jezero crater, MarsMichael W M Jones, David T Flannery, Joel A Hurowitz, et al.
Nature|May 13, 2021
An aged immune system drives senescence and ageing of solid organsMatthew J Yousefzadeh, Rafael R Flores, Yi Zhu, et al.
Science Advances|July 2, 2025
In situ evidence for serpentinization within the Máaz formation, Jezero crater, MarsNicholas J Tosca, Michael M Tice, Joel A Hurowitz, et al.
Global Health, Epidemiology and Genomics|December 26, 2017
H3Africa AWI-Gen Collaborative Centre: a resource to study the interplay between genomic and environmental risk factors for cardiometabolic diseases in four sub-Saharan African countriesM Ramsay, N Crowther, E Tambo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 18, 2019
Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basisKarin Weiss, Hayley P Lazar, Alina Kurolap, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 8, 2019
The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basisKarin Weiss, Hayley P Lazar, Alina Kurolap, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaborationDuncan S Palmer, Barney Hill, Sam Hodgson, et al.
Science (New York, N.Y.)|August 25, 2022
An olivine cumulate outcrop on the floor of Jezero crater, MarsY Liu, M M Tice, M E Schmidt, et al.
Nature Communications|February 17, 2019
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and languageLot Snijders Blok, Justine Rousseau, Joanna Twist, et al.
Pageof 68