Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Don, Keiller"'
Autor:
Dan Gordon, Don Keiller
Publikováno v:
Journal of Science and Medicine in Sport. 23:506-511
Objectives This study tests the hypothesis that individuals who achieve a plateau at V ˙ O2max ( V ˙ O2plat) are more likely to possess alleles, associated with anaerobic capacity, than those who do not. Design A literature survey, physiological te
Publikováno v:
The Journal of Sports Medicine and Physical Fitness. 60
BACKGROUND Sprint interval training is a popular workout modality. Studies have eluded to a positive effect on maximal oxygen uptake, however little is known about the mechanistic basis of this adaptation. Therefore, the purpose of this study was to
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 10, p e0249501 (2021)
PLoS ONE, Vol 16, Iss 10, p e0249501 (2021)
The aim of this systematic review and meta-analysis was to identify a list of common, candidate genes associated with the three components of fitness, specifically cardiovascular fitness, muscular strength, and anaerobic power, and how these genes ar
Autor:
Charles A, Steward, Jolien, Roovers, Marie-Marthe, Suner, Jose M, Gonzalez, Barbara, Uszczynska-Ratajczak, Dmitri, Pervouchine, Stephen, Fitzgerald, Margarida, Viola, Hannah, Stamberger, Fadi F, Hamdan, Berten, Ceulemans, Patricia, Leroy, Caroline, Nava, Anne, Lepine, Electra, Tapanari, Don, Keiller, Stephen, Abbs, Alba, Sanchis-Juan, Detelina, Grozeva, Anthony S, Rogers, Mark, Diekhans, Roderic, Guigó, Robert, Petryszak, Berge A, Minassian, Gianpiero, Cavalleri, Dimitrios, Vitsios, Slavé, Petrovski, Jennifer, Harrow, Paul, Flicek, F, Lucy Raymond, Nicholas J, Lench, Peter De, Jonghe, Jonathan M, Mudge, Sarah, Weckhuysen, Sanjay M, Sisodiya, Adam, Frankish
Publikováno v:
NPJ Genomic Medicine
The developmental and epileptic encephalopathies (DEE) are a group of rare, severe neurodevelopmental disorders, where even the most thorough sequencing studies leave 60–65% of patients without a molecular diagnosis. Here, we explore the incomplete
Autor:
Stephen Abbs, Caroline Nava, Sanjay M. Sisodiya, Jyoti S. Choudhary, Dimitrios Vitsios, Dmitri D. Pervouchine, Electra Tapanari, Fadi F. Hamdan, Hannah Stamberger, Berten Ceulemans, Detelina Grozeva, Jennifer Harrow, Patricia Leroy, Marie Marthe Suner, Charles A. Steward, Gianpiero L. Cavalleri, Margarida Viola, Anne Fabienne Lepine, José M. González, Mark Diekhans, Barbara Uszczynska-Ratajczak, Paul Flicek, Nicholas Lench, F. Lucy Raymond, Adam Frankish, Robert Petryszak, Stephen Fitzgerald, Sarah Weckhuysen, Alba Sanchis-Juan, James C. Wright, Peter De Jonghe, Roderic Guigó, Anthony Rogers, Slavé Petrovski, Don Keiller, Jonathan M. Mudge, Jolien Roovers, Berge A. Minassian
The early infantile epileptic encephalopathies (EIEE) are a group of rare, severe neurodevelopmental disorders, where even the most thorough sequencing studies leave 60-65% of patients without a molecular diagnosis. Here, we explore the incompletenes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b19da24628aeae9fad19e53f09c9ec01
Autor:
Stephen Abbs, Dimitrios Vitsios, Dmitri D. Pervouchine, Paul Flicek, Hannah Stamberger, Roderic Guigó, Barbara Uszczynska-Ratajczak, F. Lucy Raymond, Margarida Viola, Jennifer Harrow, Adam Frankish, Robert Petryszak, Sarah Weckhuysen, Alba Sanchis-Juan, Caroline Nava, Electra Tapanari, José M. González, Anthony Rogers, Slavé Petrovski, Anne Fabienne Lepine, Patricia Leroy, Detelina Grozeva, Marie Marthe Suner, Mark Diekhans, Gianpiero L. Cavalleri, Don Keiller, Berten Ceulemans, Nicholas Lench, Jonathan M. Mudge, Jolien Roovers, Stephen Fitzgerald, Berge A. Minassian, Charles A. Steward, Peter De Jonghe, Sanjay M. Sisodiya, Fadi F. Hamdan
Publikováno v:
Npj genomic medicine
npj Genomic Medicine, Vol 4, Iss 1, Pp 1-11 (2019)
Recercat. Dipósit de la Recerca de Catalunya
instname
npj Genomic Medicine, Vol 4, Iss 1, Pp 1-11 (2019)
Recercat. Dipósit de la Recerca de Catalunya
instname
The developmental and epileptic encephalopathies (DEE) are a group of rare, severe neurodevelopmental disorders, where even the most thorough sequencing studies leave 60–65% of patients without a molecular diagnosis. Here, we explore the incomplete
Autor:
Don Keiller, Dan Gordon
This study investigates heart rate (HR), in 11 young adults (22.4±3.21yr), at V̇O2max, to ascertain whether measured maximal heart rate (HRmax), as determined by a plateau in HR (HRplat), can reliably confirm V̇O2max. V̇O2max and HRplat were dete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34d572719fcabb65789ad1d9503b32f2
https://arro.anglia.ac.uk/id/eprint/702325/1/Keiller_2017.doc
https://arro.anglia.ac.uk/id/eprint/702325/1/Keiller_2017.doc
Autor:
Dan Gordon, Oliver Caddy, Viviane Merzbach, Marie Gernigon, James Baker, Adrian Scruton, Don Keiller, Richard Barnes
Publikováno v:
Journal of Sports Science and Medicine, Vol 14, Iss 1, Pp 47-53 (2015)
The purpose of this study was to assess the VO2max plateau response at VO2max during a series of pre-determined trials. METHODS: Ten male well-trained athletes (age, 23.0 ± 3.2; height, 183.3 ± 5.5 cm; mass 77.5 ± 11.1 Kg; VO2max 66.5 ± 5.0 ml.kg
Autor:
Patrick Swain, Dan Gordon, Henry Chung, Diane Johnson, Viviane Merzbach, André Maia-Lima, Luciano Sales Prado, Don Keiller
Publikováno v:
Medicine & Science in Sports & Exercise. 51:187-187
Autor:
James Baker, Oliver Caddy, Dan Gordon, Viviane Merzbach, Andrew Porter, Madeleine Wood, Richard Barnes, Vignesh Vetrivel, Don Keiller, Marie Gernigon
Publikováno v:
European Journal of Applied Physiology. 114:21-27
The purpose of this study was to examine the effects of reductions in blood volume and associated oxygen-carrying capacity on the incidence of plateau at $$\dot{V}{\text{O}}$$ 2max. Fifteen well-trained athletes (age 23.3 ± 4.5; mass 77.4 ± 13.1 kg