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Gillian M Borthwick

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In Vitro Cellular & Developmental Biology. Animal|November 18, 2010
The H9C2 cell line and primary neonatal cardiomyocyte cells show similar hypertrophic responses in vitroSarah J Watkins, Gillian M Borthwick, Helen M Arthur
Laboratory Investigation; a Journal of Technical Methods and Pathology|November 19, 2008
Endoglin and activin receptor-like-kinase 1 are co-expressed in the distal vessels of the lung: implications for two familial vascular dysplasias, HHT and PAHMarwa Mahmoud, Gillian M Borthwick, Alison A Hislop, et al.
Hypertension Research : Official Journal of the Japanese Society of Hypertension|November 11, 2011
Angiotensin II-induced cardiomyocyte hypertrophy in vitro is TAK1-dependent and Smad2/3-independentSarah J Watkins, Gillian M Borthwick, Rachael Oakenfull, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 3, 2006
Therapeutic levels of aspirin and salicylate directly inhibit a model of angiogenesis through a Cox-independent mechanismGillian M Borthwick, A Sarah Johnson, Matthew Partington, et al.
Cancers|January 27, 2021
How Should We Test for Lynch Syndrome? A Review of Current Guidelines and Future StrategiesRichard Gallon, Peter Gawthorpe, Rachel L Phelps, et al.
The British Journal of General Practice : the Journal of the Royal College of General Practitioners|March 30, 2023
GPs' willingness to prescribe aspirin for cancer preventive therapy in Lynch syndrome: a factorial randomised trial investigating factors influencing decisionsKelly E Lloyd, Louise H Hall, Lucy Ziegler, et al.
Annals of Neurology|December 17, 2005
Motor neuron disease in a patient with a mitochondrial tRNAIle mutationGillian M Borthwick, Robert W Taylor, Timothy J Walls, et al.
Nucleic Acids Research|July 24, 2002
Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCRLangping He, Patrick F Chinnery, Steve E Durham, et al.
Mutation Research|March 26, 2003
Changes in the human mitochondrial genome after treatment of malignant diseaseTheresa M Wardell, Elaine Ferguson, Patrick F Chinnery, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular musclesPatrick Yu-Wai-Man, Joey Lai-Cheong, Gillian M Borthwick, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
In Vitro Cellular & Developmental Biology. Animal|November 18, 2010
The H9C2 cell line and primary neonatal cardiomyocyte cells show similar hypertrophic responses in vitroSarah J Watkins, Gillian M Borthwick, Helen M Arthur
Laboratory Investigation; a Journal of Technical Methods and Pathology|November 19, 2008
Endoglin and activin receptor-like-kinase 1 are co-expressed in the distal vessels of the lung: implications for two familial vascular dysplasias, HHT and PAHMarwa Mahmoud, Gillian M Borthwick, Alison A Hislop, et al.
Hypertension Research : Official Journal of the Japanese Society of Hypertension|November 11, 2011
Angiotensin II-induced cardiomyocyte hypertrophy in vitro is TAK1-dependent and Smad2/3-independentSarah J Watkins, Gillian M Borthwick, Rachael Oakenfull, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 3, 2006
Therapeutic levels of aspirin and salicylate directly inhibit a model of angiogenesis through a Cox-independent mechanismGillian M Borthwick, A Sarah Johnson, Matthew Partington, et al.
Cancers|January 27, 2021
How Should We Test for Lynch Syndrome? A Review of Current Guidelines and Future StrategiesRichard Gallon, Peter Gawthorpe, Rachel L Phelps, et al.
The British Journal of General Practice : the Journal of the Royal College of General Practitioners|March 30, 2023
GPs' willingness to prescribe aspirin for cancer preventive therapy in Lynch syndrome: a factorial randomised trial investigating factors influencing decisionsKelly E Lloyd, Louise H Hall, Lucy Ziegler, et al.
Annals of Neurology|December 17, 2005
Motor neuron disease in a patient with a mitochondrial tRNAIle mutationGillian M Borthwick, Robert W Taylor, Timothy J Walls, et al.
Nucleic Acids Research|July 24, 2002
Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCRLangping He, Patrick F Chinnery, Steve E Durham, et al.
Mutation Research|March 26, 2003
Changes in the human mitochondrial genome after treatment of malignant diseaseTheresa M Wardell, Elaine Ferguson, Patrick F Chinnery, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular musclesPatrick Yu-Wai-Man, Joey Lai-Cheong, Gillian M Borthwick, et al.
Pageof 2