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L Bindoff

Showing results (11-20 of 22) with videos related to

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European Journal of Human Genetics : EJHG|November 26, 1999
A common disease haplotype segregating in spinocerebellar ataxia 2 (SCA2) pedigrees of diverse ethnic originJ Pang, R Allotey, N Wadia, et al.
Human Molecular Genetics|January 1, 1993
Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate formJ Poulton, M E Deadman, L Bindoff, et al.
Brain : a Journal of Neurology|May 13, 1998
Abnormal merosin in adults. A new form of late onset muscular dystrophy not linked to chromosome 6q2K Bushby, L V Anderson, C Pollitt, et al.
Nature Communications|October 12, 2019
Marine nitrogen fixers mediate a low latitude pathway for atmospheric CO<sub>2</sub> drawdownPearse J Buchanan, Zanna Chase, Richard J Matear, et al.
Muscle & Nerve. Supplement|January 1, 1995
Duplications of mitochondrial DNA in Kearns-Sayre syndromeJ Poulton, K J Morten, D Marchington, et al.
Nature|August 22, 2000
Ocean circulation off east Antarctica affects ecosystem structure and sea-ice extentS Nicol, T Pauly, N L Bindoff, et al.
American Journal of Medical Genetics|July 16, 1999
Nonrandom tissue distribution of mutant mtDNAP F Chinnery, P J Zwijnenburg, M Walker, et al.
Plos One|November 25, 2014
Improving the use of species distribution models in conservation planning and management under climate changeLuciana L Porfirio, Rebecca M B Harris, Edward C Lefroy, et al.
Nature Communications|July 15, 2017
The unprecedented 2015/16 Tasman Sea marine heatwaveEric C J Oliver, Jessica A Benthuysen, Nathaniel L Bindoff, et al.
Annals of Neurology|August 12, 1999
Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiencyV Tiranti, M Jaksch, S Hofmann, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
European Journal of Human Genetics : EJHG|November 26, 1999
A common disease haplotype segregating in spinocerebellar ataxia 2 (SCA2) pedigrees of diverse ethnic originJ Pang, R Allotey, N Wadia, et al.
Human Molecular Genetics|January 1, 1993
Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate formJ Poulton, M E Deadman, L Bindoff, et al.
Brain : a Journal of Neurology|May 13, 1998
Abnormal merosin in adults. A new form of late onset muscular dystrophy not linked to chromosome 6q2K Bushby, L V Anderson, C Pollitt, et al.
Nature Communications|October 12, 2019
Marine nitrogen fixers mediate a low latitude pathway for atmospheric CO<sub>2</sub> drawdownPearse J Buchanan, Zanna Chase, Richard J Matear, et al.
Muscle & Nerve. Supplement|January 1, 1995
Duplications of mitochondrial DNA in Kearns-Sayre syndromeJ Poulton, K J Morten, D Marchington, et al.
Nature|August 22, 2000
Ocean circulation off east Antarctica affects ecosystem structure and sea-ice extentS Nicol, T Pauly, N L Bindoff, et al.
American Journal of Medical Genetics|July 16, 1999
Nonrandom tissue distribution of mutant mtDNAP F Chinnery, P J Zwijnenburg, M Walker, et al.
Plos One|November 25, 2014
Improving the use of species distribution models in conservation planning and management under climate changeLuciana L Porfirio, Rebecca M B Harris, Edward C Lefroy, et al.
Nature Communications|July 15, 2017
The unprecedented 2015/16 Tasman Sea marine heatwaveEric C J Oliver, Jessica A Benthuysen, Nathaniel L Bindoff, et al.
Annals of Neurology|August 12, 1999
Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiencyV Tiranti, M Jaksch, S Hofmann, et al.
Pageof 3