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J Coull

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Experimental Dermatology|March 24, 2018
A rare missense mutation in GJB3 (Cx31G45E) is associated with a unique cellular phenotype resulting in necrotic cell deathJennifer A Easton, Ahmad K Albuloushi, Miriam A F Kamps, et al.
Autophagy|August 16, 2014
FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylationElaine A Dunlop, Sara Seifan, Tijs Claessens, et al.
Oncogene|March 26, 2025
Characterizing the tumor suppressor activity of FLCN in Birt-Hogg-Dubé syndrome cell models through transcriptomic and proteomic analysisRachel-Ann Jones, Elaine A Dunlop, Jesse D Champion, et al.
Lancet (London, England)|June 15, 2004
Change in stroke incidence, mortality, case-fatality, severity, and risk factors in Oxfordshire, UK from 1981 to 2004 (Oxford Vascular Study)P M Rothwell, A J Coull, M F Giles, et al.
Lancet (London, England)|November 22, 2005
Population-based study of event-rate, incidence, case fatality, and mortality for all acute vascular events in all arterial territories (Oxford Vascular Study)P M Rothwell, A J Coull, L E Silver, et al.
Familial Cancer|December 25, 2012
A de novo FLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluationFred H Menko, Paul C Johannesma, R Jeroen A van Moorselaar, et al.
The Journal of Clinical Investigation|April 26, 2014
The tumor suppressor folliculin regulates AMPK-dependent metabolic transformationMing Yan, Marie-Claude Gingras, Elaine A Dunlop, et al.
Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine|December 14, 2023
Pre-hospital ECPR in an Australian metropolitan setting: a single-arm feasibility assessment-The CPR, pre-hospital ECPR and early reperfusion (CHEER3) studyS A C Richardson, D Anderson, A J C Burrell, et al.
Human Molecular Genetics|June 21, 2013
Birt-Hogg-Dube syndrome is a novel ciliopathyMonique N H Luijten, Sander G Basten, Tijs Claessens, et al.
Human Molecular Genetics|May 10, 2018
Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotypeIvo J H M de Vos, Evelyn Yaqiong Tao, Sheena Li Ming Ong, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Experimental Dermatology|March 24, 2018
A rare missense mutation in GJB3 (Cx31G45E) is associated with a unique cellular phenotype resulting in necrotic cell deathJennifer A Easton, Ahmad K Albuloushi, Miriam A F Kamps, et al.
Autophagy|August 16, 2014
FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylationElaine A Dunlop, Sara Seifan, Tijs Claessens, et al.
Oncogene|March 26, 2025
Characterizing the tumor suppressor activity of FLCN in Birt-Hogg-Dubé syndrome cell models through transcriptomic and proteomic analysisRachel-Ann Jones, Elaine A Dunlop, Jesse D Champion, et al.
Lancet (London, England)|June 15, 2004
Change in stroke incidence, mortality, case-fatality, severity, and risk factors in Oxfordshire, UK from 1981 to 2004 (Oxford Vascular Study)P M Rothwell, A J Coull, M F Giles, et al.
Lancet (London, England)|November 22, 2005
Population-based study of event-rate, incidence, case fatality, and mortality for all acute vascular events in all arterial territories (Oxford Vascular Study)P M Rothwell, A J Coull, L E Silver, et al.
Familial Cancer|December 25, 2012
A de novo FLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluationFred H Menko, Paul C Johannesma, R Jeroen A van Moorselaar, et al.
The Journal of Clinical Investigation|April 26, 2014
The tumor suppressor folliculin regulates AMPK-dependent metabolic transformationMing Yan, Marie-Claude Gingras, Elaine A Dunlop, et al.
Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine|December 14, 2023
Pre-hospital ECPR in an Australian metropolitan setting: a single-arm feasibility assessment-The CPR, pre-hospital ECPR and early reperfusion (CHEER3) studyS A C Richardson, D Anderson, A J C Burrell, et al.
Human Molecular Genetics|June 21, 2013
Birt-Hogg-Dube syndrome is a novel ciliopathyMonique N H Luijten, Sander G Basten, Tijs Claessens, et al.
Human Molecular Genetics|May 10, 2018
Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotypeIvo J H M de Vos, Evelyn Yaqiong Tao, Sheena Li Ming Ong, et al.
Pageof 5