Gillian M Borthwick

Gillian M Borthwick

UNVERIFIED PROFILE

Are you Gillian M Borthwick?   Register this Author

Register author
Gillian M Borthwick

Gillian M Borthwick

Publications by authors named "Gillian M Borthwick"

Are you Gillian M Borthwick?   Register this Author

11Publications

54Reads

25Profile Views

Angiotensin II-induced cardiomyocyte hypertrophy in vitro is TAK1-dependent and Smad2/3-independent.

Hypertens Res 2012 Apr 10;35(4):393-8. Epub 2011 Nov 10.

Institute of Human Genetics, Centre for Life, Newcastle University, Newcastle, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/hr.2011.196DOI Listing
April 2012

The H9C2 cell line and primary neonatal cardiomyocyte cells show similar hypertrophic responses in vitro.

In Vitro Cell Dev Biol Anim 2011 Feb 17;47(2):125-31. Epub 2010 Nov 17.

Institute of Human Genetics, Newcastle University, Newcastle, NE1 3BZ, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s11626-010-9368-1DOI Listing
February 2011

Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular muscles.

Invest Ophthalmol Vis Sci 2010 Jul 17;51(7):3347-53. Epub 2010 Feb 17.

Mitochondrial Research Group, Institute for Ageing and Health, The Medical School, Newcastle University, Newcastle-upon-Tyne, United Kingdom.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1167/iovs.09-4660DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2904001PMC
July 2010

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 PAH.

Lab Invest 2009 Jan 17;89(1):15-25. Epub 2008 Nov 17.

Institute of Human Genetics, Centre for Life, Newcastle University, Newcastle upon Tyne, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/labinvest.2008.112DOI Listing
January 2009

Therapeutic levels of aspirin and salicylate directly inhibit a model of angiogenesis through a Cox-independent mechanism.

FASEB J 2006 Oct;20(12):2009-16

Institute of Human Genetics, International Centre for Life, University of Newcastle, NE1 3BZ, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1096/fj.06-5987comDOI Listing
October 2006

Motor neuron disease in a patient with a mitochondrial tRNAIle mutation.

Ann Neurol 2006 Mar;59(3):570-4

Mitochondrial Research Group, School of Neurology, Neurobiology and Psychiatry, The Medical School, University of Newcastle upon Tyne, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ana.20758DOI Listing
March 2006

Changes in the human mitochondrial genome after treatment of malignant disease.

Mutat Res 2003 Apr;525(1-2):19-27

Department of Neurology, The Medical School, University of Newcastle upon Tyne, Newcastle upon Tyne NE2 4HH, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0027-5107(02)00313-5DOI Listing
April 2003

Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR.

Nucleic Acids Res 2002 Jul;30(14):e68

Department of Neurology, The Medical School, University of Newcastle upon Tyne, Framlington Place, Newcastle upon Tyne NE2 4HH, UK.

View Article

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC135769PMC
http://dx.doi.org/10.1093/nar/gnf067DOI Listing
July 2002