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Martin J Barron

Showing results (1-10 of 18) with videos related to

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Orphanet Journal of Rare Diseases|November 22, 2008
Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasiaMartin J Barron, Sinead T McDonnell, Iain Mackie, et al.
Frontiers in Physiology|September 28, 2017
The Unfolded Protein Response in Amelogenesis and Enamel PathologiesSteven J Brookes, Martin J Barron, Michael J Dixon, et al.
Human Molecular Genetics|December 24, 2013
Endoplasmic reticulum stress in amelogenesis imperfecta and phenotypic rescue using 4-phenylbutyrateSteven J Brookes, Martin J Barron, Ray Boot-Handford, et al.
Neuromuscular Disorders : NMD|March 17, 2004
The diagnosis of mitochondrial muscle diseaseRobert W Taylor, Andrew M Schaefer, Martin J Barron, et al.
European Journal of Oral Sciences|January 17, 2012
Is the 32-kDa fragment the functional enamelin unit in all species?Steven J Brookes, Nicola J Kingswell, Martin J Barron, et al.
Mechanisms of Ageing and Development|October 22, 2011
Differences in the accumulation of mitochondrial defects with age in mice and humansLaura C Greaves, Martin J Barron, George Campbell-Shiel, et al.
Human Molecular Genetics|August 16, 2008
The cell adhesion molecule nectin-1 is critical for normal enamel formation in miceMartin J Barron, Steven J Brookes, Clare E Draper, et al.
Experimental Gerontology|January 26, 2010
Defects in multiple complexes of the respiratory chain are present in ageing human colonic cryptsLaura C Greaves, Martin J Barron, Stefan Plusa, et al.
Brain : a Journal of Neurology|November 7, 2006
Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletionsTanja Taivassalo, Julie L Gardner, Robert W Taylor, et al.
Human Molecular Genetics|January 14, 2010
A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfectaMartin J Barron, Steven J Brookes, Jennifer Kirkham, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Orphanet Journal of Rare Diseases|November 22, 2008
Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasiaMartin J Barron, Sinead T McDonnell, Iain Mackie, et al.
Frontiers in Physiology|September 28, 2017
The Unfolded Protein Response in Amelogenesis and Enamel PathologiesSteven J Brookes, Martin J Barron, Michael J Dixon, et al.
Human Molecular Genetics|December 24, 2013
Endoplasmic reticulum stress in amelogenesis imperfecta and phenotypic rescue using 4-phenylbutyrateSteven J Brookes, Martin J Barron, Ray Boot-Handford, et al.
Neuromuscular Disorders : NMD|March 17, 2004
The diagnosis of mitochondrial muscle diseaseRobert W Taylor, Andrew M Schaefer, Martin J Barron, et al.
European Journal of Oral Sciences|January 17, 2012
Is the 32-kDa fragment the functional enamelin unit in all species?Steven J Brookes, Nicola J Kingswell, Martin J Barron, et al.
Mechanisms of Ageing and Development|October 22, 2011
Differences in the accumulation of mitochondrial defects with age in mice and humansLaura C Greaves, Martin J Barron, George Campbell-Shiel, et al.
Human Molecular Genetics|August 16, 2008
The cell adhesion molecule nectin-1 is critical for normal enamel formation in miceMartin J Barron, Steven J Brookes, Clare E Draper, et al.
Experimental Gerontology|January 26, 2010
Defects in multiple complexes of the respiratory chain are present in ageing human colonic cryptsLaura C Greaves, Martin J Barron, Stefan Plusa, et al.
Brain : a Journal of Neurology|November 7, 2006
Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletionsTanja Taivassalo, Julie L Gardner, Robert W Taylor, et al.
Human Molecular Genetics|January 14, 2010
A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfectaMartin J Barron, Steven J Brookes, Jennifer Kirkham, et al.
Pageof 2