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Paula Carroll

Showing results (21-30 of 34) with videos related to

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BMC Medical Research Methodology|October 7, 2020
Recruiting men from across the socioeconomic spectrum via GP registers and community outreach to a weight management feasibility randomised controlled trialMatthew D McDonald, Stephan U Dombrowski, Rebecca Skinner, et al.
Health Technology Assessment (Winchester, England)|May 27, 2014
Systematic reviews of and integrated report on the quantitative, qualitative and economic evidence base for the management of obesity in menClare Robertson, Daryll Archibald, Alison Avenell, et al.
The EMBO Journal|February 24, 2016
Ribonuclease H2 mutations induce a cGAS/STING-dependent innate immune responseKaren J Mackenzie, Paula Carroll, Laura Lettice, et al.
BMJ Open|February 28, 2020
Game of Stones: feasibility randomised controlled trial of how to engage men with obesity in text message and incentive interventions for weight lossStephan U Dombrowski, Matthew McDonald, Marjon van der Pol, et al.
Nature|July 25, 2017
cGAS surveillance of micronuclei links genome instability to innate immunityKaren J Mackenzie, Paula Carroll, Carol-Anne Martin, et al.
Trials|July 22, 2022
Effectiveness and cost-effectiveness of text messages with or without endowment incentives for weight management in men with obesity (Game of Stones): study protocol for a randomised controlled trialLisa Macaulay, Catriona O'Dolan, Alison Avenell, et al.
Genes & Development|October 16, 2020
PRIM1 deficiency causes a distinctive primordial dwarfism syndromeDavid A Parry, Lukas Tamayo-Orrego, Paula Carroll, et al.
Nature|February 10, 2022
Signatures of TOP1 transcription-associated mutagenesis in cancer and germlineMartin A M Reijns, David A Parry, Thomas C Williams, et al.
Nature|May 3, 2022
Publisher Correction: Signatures of TOP1 transcription-associated mutagenesis in cancer and germlineMartin A M Reijns, David A Parry, Thomas C Williams, et al.
American Journal of Human Genetics|March 3, 2015
Mutations in the NHEJ component XRCC4 cause primordial dwarfismJennie E Murray, Mirjam van der Burg, Hanna IJspeert, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
BMC Medical Research Methodology|October 7, 2020
Recruiting men from across the socioeconomic spectrum via GP registers and community outreach to a weight management feasibility randomised controlled trialMatthew D McDonald, Stephan U Dombrowski, Rebecca Skinner, et al.
Health Technology Assessment (Winchester, England)|May 27, 2014
Systematic reviews of and integrated report on the quantitative, qualitative and economic evidence base for the management of obesity in menClare Robertson, Daryll Archibald, Alison Avenell, et al.
The EMBO Journal|February 24, 2016
Ribonuclease H2 mutations induce a cGAS/STING-dependent innate immune responseKaren J Mackenzie, Paula Carroll, Laura Lettice, et al.
BMJ Open|February 28, 2020
Game of Stones: feasibility randomised controlled trial of how to engage men with obesity in text message and incentive interventions for weight lossStephan U Dombrowski, Matthew McDonald, Marjon van der Pol, et al.
Nature|July 25, 2017
cGAS surveillance of micronuclei links genome instability to innate immunityKaren J Mackenzie, Paula Carroll, Carol-Anne Martin, et al.
Trials|July 22, 2022
Effectiveness and cost-effectiveness of text messages with or without endowment incentives for weight management in men with obesity (Game of Stones): study protocol for a randomised controlled trialLisa Macaulay, Catriona O'Dolan, Alison Avenell, et al.
Genes & Development|October 16, 2020
PRIM1 deficiency causes a distinctive primordial dwarfism syndromeDavid A Parry, Lukas Tamayo-Orrego, Paula Carroll, et al.
Nature|February 10, 2022
Signatures of TOP1 transcription-associated mutagenesis in cancer and germlineMartin A M Reijns, David A Parry, Thomas C Williams, et al.
Nature|May 3, 2022
Publisher Correction: Signatures of TOP1 transcription-associated mutagenesis in cancer and germlineMartin A M Reijns, David A Parry, Thomas C Williams, et al.
American Journal of Human Genetics|March 3, 2015
Mutations in the NHEJ component XRCC4 cause primordial dwarfismJennie E Murray, Mirjam van der Burg, Hanna IJspeert, et al.
Pageof 4