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S Brooks

Showing results (621-630 of 728) with videos related to

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Neurology. Genetics|December 13, 2021
Confirming Pathogenicity of the F386L <i>PSEN1</i> Variant in a South Asian Family With Early-Onset Alzheimer DiseaseSarah J Eger, Yann Le Guen, Raiyan R Khan, et al.
Cancer Immunology Research|June 26, 2020
Distinctive Subpopulations of Stromal Cells Are Present in Human Lymph Nodes Infiltrated with MelanomaJennifer Eom, Saem Mul Park, Vaughan Feisst, et al.
Human Reproduction (Oxford, England)|January 7, 2017
Previous miscarriages and GLI2 are associated with anorectal malformations in offspringRomy van de Putte, Charlotte H W Wijers, Ivo de Blaauw, et al.
Kidney Medicine|May 25, 2023
Dietary Patterns, Apolipoprotein L1 Risk Genotypes, and CKD Outcomes Among Black Adults in the Reasons for Geographic and Racial Differences in Stroke (REGARDS) Cohort StudyTitilayo O Ilori, Marquita S Brooks, Parin N Desai, et al.
Human Molecular Genetics|August 18, 2022
The long Filamin-A isoform is required for intestinal development and motility: implications for chronic intestinal pseudo-obstructionAlmira Zada, Yuying Zhao, Danny Halim, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|April 23, 2023
Higher systolic blood pressure in early-mid adulthood is associated with poorer cognitive performance in those with a dominantly inherited Alzheimer's disease mutation but not in non-carriers. Results from the DIAN studyYing Xu, Htein Linn Aung, Randall J Bateman, et al.
Nature Communications|March 30, 2016
Interplanar coupling-dependent magnetoresistivity in high-purity layered metalsN Kikugawa, P Goswami, A Kiswandhi, et al.
Medical Science Educator|February 23, 2022
Back to the Future: Maximizing Student Learning and Wellbeing in the Virtual AgeAndrea N Belovich, Ingrid Bahner, Giulia Bonaminio, et al.
Brain : a Journal of Neurology|October 31, 2006
Mutations in progranulin explain atypical phenotypes with variants in MAPTStuart M Pickering-Brown, Matt Baker, Jenny Gass, et al.
Scientific Reports|November 11, 2020
Mir142 loss unlocks IDH2<sup>R140</sup>-dependent leukemogenesis through antagonistic regulation of HOX genesA Marshall, J Kasturiarachchi, P Datta, et al.
Pageof 73

Showing results (621-630 of 728) with videos related to

Sort By:
Pageof 73
Neurology. Genetics|December 13, 2021
Confirming Pathogenicity of the F386L <i>PSEN1</i> Variant in a South Asian Family With Early-Onset Alzheimer DiseaseSarah J Eger, Yann Le Guen, Raiyan R Khan, et al.
Cancer Immunology Research|June 26, 2020
Distinctive Subpopulations of Stromal Cells Are Present in Human Lymph Nodes Infiltrated with MelanomaJennifer Eom, Saem Mul Park, Vaughan Feisst, et al.
Human Reproduction (Oxford, England)|January 7, 2017
Previous miscarriages and GLI2 are associated with anorectal malformations in offspringRomy van de Putte, Charlotte H W Wijers, Ivo de Blaauw, et al.
Kidney Medicine|May 25, 2023
Dietary Patterns, Apolipoprotein L1 Risk Genotypes, and CKD Outcomes Among Black Adults in the Reasons for Geographic and Racial Differences in Stroke (REGARDS) Cohort StudyTitilayo O Ilori, Marquita S Brooks, Parin N Desai, et al.
Human Molecular Genetics|August 18, 2022
The long Filamin-A isoform is required for intestinal development and motility: implications for chronic intestinal pseudo-obstructionAlmira Zada, Yuying Zhao, Danny Halim, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|April 23, 2023
Higher systolic blood pressure in early-mid adulthood is associated with poorer cognitive performance in those with a dominantly inherited Alzheimer's disease mutation but not in non-carriers. Results from the DIAN studyYing Xu, Htein Linn Aung, Randall J Bateman, et al.
Nature Communications|March 30, 2016
Interplanar coupling-dependent magnetoresistivity in high-purity layered metalsN Kikugawa, P Goswami, A Kiswandhi, et al.
Medical Science Educator|February 23, 2022
Back to the Future: Maximizing Student Learning and Wellbeing in the Virtual AgeAndrea N Belovich, Ingrid Bahner, Giulia Bonaminio, et al.
Brain : a Journal of Neurology|October 31, 2006
Mutations in progranulin explain atypical phenotypes with variants in MAPTStuart M Pickering-Brown, Matt Baker, Jenny Gass, et al.
Scientific Reports|November 11, 2020
Mir142 loss unlocks IDH2<sup>R140</sup>-dependent leukemogenesis through antagonistic regulation of HOX genesA Marshall, J Kasturiarachchi, P Datta, et al.
Pageof 73