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M Cowan

Showing results (871-880 of 886) with videos related to

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Nature Genetics|July 18, 2006
Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locusYanick J Crow, Bruce E Hayward, Rekha Parmar, et al.
British Journal of Sports Medicine|May 6, 2026
Supported implementation enhances injury prevention programme (Prep-to-Play) use in women and girls playing Australian Football: a pragmatic type III hybrid implementation-effectiveness stepped wedge cluster randomised trialBrooke E Patterson, Nicole M White, Sallie M Cowan, et al.
Nature Aging|April 28, 2023
Microbiota from young mice counteracts selective age-associated behavioral deficitsMarcus Boehme, Katherine E Guzzetta, Thomaz F S Bastiaanssen, et al.
Journal for Immunotherapy of Cancer|October 29, 2020
Genetically engineered macrophages persist in solid tumors and locally deliver therapeutic proteins to activate immune responsesKatherine J Brempelis, Courtney M Cowan, Shannon A Kreuser, et al.
BMJ Open|September 14, 2022
Evaluation of an injury prevention programme (Prep-to-Play) in women and girls playing Australian Football: design of a pragmatic, type III, hybrid implementation-effectiveness, stepped-wedge, cluster randomised controlled trialBrooke E Patterson, Alex Donaldson, Sallie M Cowan, et al.
British Journal of Sports Medicine|November 5, 2025
Dissemination and implementation of injury prevention interventions: a scoping review for the Female, woman and/or girl Athlete Injury pRevention (FAIR) consensusBrooke E Patterson, Carly D McKay, Meghan L Critchley, et al.
Biorxiv : the Preprint Server for Biology|March 23, 2026
Aberrant oxidative metabolism selects for <i>TET2</i> -deficient hematopoietic stem and progenitor cellsKatia E Niño, Vera Adema, Alyx E Gray, et al.
Biorxiv : the Preprint Server for Biology|January 3, 2024
The Natural Products Discovery Center: Release of the First 8490 Sequenced Strains for Exploring Actinobacteria Biosynthetic DiversityEdward Kalkreuter, Satria A Kautsar, Dong Yang, et al.
The Journal of Biological Chemistry|June 16, 2012
Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle diseaseEloisa Carta, Seo-Kyung Chung, Victoria M James, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2014
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathwayGregory M Enns, Vandana Shashi, Matthew Bainbridge, et al.
Pageof 89

Showing results (871-880 of 886) with videos related to

Sort By:
Pageof 89
Nature Genetics|July 18, 2006
Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locusYanick J Crow, Bruce E Hayward, Rekha Parmar, et al.
British Journal of Sports Medicine|May 6, 2026
Supported implementation enhances injury prevention programme (Prep-to-Play) use in women and girls playing Australian Football: a pragmatic type III hybrid implementation-effectiveness stepped wedge cluster randomised trialBrooke E Patterson, Nicole M White, Sallie M Cowan, et al.
Nature Aging|April 28, 2023
Microbiota from young mice counteracts selective age-associated behavioral deficitsMarcus Boehme, Katherine E Guzzetta, Thomaz F S Bastiaanssen, et al.
Journal for Immunotherapy of Cancer|October 29, 2020
Genetically engineered macrophages persist in solid tumors and locally deliver therapeutic proteins to activate immune responsesKatherine J Brempelis, Courtney M Cowan, Shannon A Kreuser, et al.
BMJ Open|September 14, 2022
Evaluation of an injury prevention programme (Prep-to-Play) in women and girls playing Australian Football: design of a pragmatic, type III, hybrid implementation-effectiveness, stepped-wedge, cluster randomised controlled trialBrooke E Patterson, Alex Donaldson, Sallie M Cowan, et al.
British Journal of Sports Medicine|November 5, 2025
Dissemination and implementation of injury prevention interventions: a scoping review for the Female, woman and/or girl Athlete Injury pRevention (FAIR) consensusBrooke E Patterson, Carly D McKay, Meghan L Critchley, et al.
Biorxiv : the Preprint Server for Biology|March 23, 2026
Aberrant oxidative metabolism selects for <i>TET2</i> -deficient hematopoietic stem and progenitor cellsKatia E Niño, Vera Adema, Alyx E Gray, et al.
Biorxiv : the Preprint Server for Biology|January 3, 2024
The Natural Products Discovery Center: Release of the First 8490 Sequenced Strains for Exploring Actinobacteria Biosynthetic DiversityEdward Kalkreuter, Satria A Kautsar, Dong Yang, et al.
The Journal of Biological Chemistry|June 16, 2012
Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle diseaseEloisa Carta, Seo-Kyung Chung, Victoria M James, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2014
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathwayGregory M Enns, Vandana Shashi, Matthew Bainbridge, et al.
Pageof 89