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Sean Ennis

Showing results (31-40 of 58) with videos related to

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Scientific Reports|December 10, 2017
The Irish DNA Atlas: Revealing Fine-Scale Population Structure and History within IrelandEdmund Gilbert, Seamus O'Reilly, Michael Merrigan, et al.
Journal of Neurology|June 17, 2017
A novel gain-of-function mutation in the ITPR1 suppressor domain causes spinocerebellar ataxia with altered Ca<sup>2+</sup> signal patternsJillian P Casey, Taisei Hirouchi, Chihiro Hisatsune, et al.
Human Molecular Genetics|February 25, 2016
Recessive NEK9 mutation causes a lethal skeletal dysplasia with evidence of cell cycle and ciliary defectsJillian P Casey, Kieran Brennan, Noemie Scheidel, et al.
Epilepsia|May 16, 2014
Towards the identification of a genetic basis for Landau-Kleffner syndromeJudith Conroy, Paul A McGettigan, Dara McCreary, et al.
Nature Genetics|February 28, 2006
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosisMatthew J Greenway, Peter M Andersen, Carsten Russ, et al.
Human Mutation|September 9, 2011
First implication of STRA6 mutations in isolated anophthalmia, microphthalmia, and coloboma: a new dimension to the STRA6 phenotypeJillian Casey, Riki Kawaguchi, Maria Morrissey, et al.
Molecular Nutrition & Food Research|April 18, 2018
Personalized Cardio-Metabolic Responses to an Anti-Inflammatory Nutrition Intervention in Obese Adolescents: A Randomized Controlled Crossover TrialAoibheann M McMorrow, Ruth M Connaughton, Tiago R Magalhães, et al.
HRB Open Research|December 11, 2020
Rare Disease Research Partnership (RAinDRoP): a collaborative approach to identify research priorities for rare diseases in IrelandSuja Somanadhan, Emma Nicholson, Emma Dorris, et al.
Clinical Transplantation|February 26, 2013
A genome-wide association study of recipient genotype and medium-term kidney allograft functionRobert P O'Brien, Paul J Phelan, Judith Conroy, et al.
European Journal of Human Genetics : EJHG|January 27, 2011
The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growthSally Ann Lynch, Nicola Foulds, Ann-Charlotte Thuresson, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Scientific Reports|December 10, 2017
The Irish DNA Atlas: Revealing Fine-Scale Population Structure and History within IrelandEdmund Gilbert, Seamus O'Reilly, Michael Merrigan, et al.
Journal of Neurology|June 17, 2017
A novel gain-of-function mutation in the ITPR1 suppressor domain causes spinocerebellar ataxia with altered Ca<sup>2+</sup> signal patternsJillian P Casey, Taisei Hirouchi, Chihiro Hisatsune, et al.
Human Molecular Genetics|February 25, 2016
Recessive NEK9 mutation causes a lethal skeletal dysplasia with evidence of cell cycle and ciliary defectsJillian P Casey, Kieran Brennan, Noemie Scheidel, et al.
Epilepsia|May 16, 2014
Towards the identification of a genetic basis for Landau-Kleffner syndromeJudith Conroy, Paul A McGettigan, Dara McCreary, et al.
Nature Genetics|February 28, 2006
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosisMatthew J Greenway, Peter M Andersen, Carsten Russ, et al.
Human Mutation|September 9, 2011
First implication of STRA6 mutations in isolated anophthalmia, microphthalmia, and coloboma: a new dimension to the STRA6 phenotypeJillian Casey, Riki Kawaguchi, Maria Morrissey, et al.
Molecular Nutrition & Food Research|April 18, 2018
Personalized Cardio-Metabolic Responses to an Anti-Inflammatory Nutrition Intervention in Obese Adolescents: A Randomized Controlled Crossover TrialAoibheann M McMorrow, Ruth M Connaughton, Tiago R Magalhães, et al.
HRB Open Research|December 11, 2020
Rare Disease Research Partnership (RAinDRoP): a collaborative approach to identify research priorities for rare diseases in IrelandSuja Somanadhan, Emma Nicholson, Emma Dorris, et al.
Clinical Transplantation|February 26, 2013
A genome-wide association study of recipient genotype and medium-term kidney allograft functionRobert P O'Brien, Paul J Phelan, Judith Conroy, et al.
European Journal of Human Genetics : EJHG|January 27, 2011
The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growthSally Ann Lynch, Nicola Foulds, Ann-Charlotte Thuresson, et al.
Pageof 6