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of 15
pro vyhledávání: '"Jo Poulton"'
Autor:
Iain G Johnston, Joerg P Burgstaller, Vitezslav Havlicek, Thomas Kolbe, Thomas Rülicke, Gottfried Brem, Jo Poulton, Nick S Jones
Publikováno v:
eLife, Vol 4 (2015)
Dangerous damage to mitochondrial DNA (mtDNA) can be ameliorated during mammalian development through a highly debated mechanism called the mtDNA bottleneck. Uncertainty surrounding this process limits our ability to address inherited mtDNA diseases.
Externí odkaz:
https://doaj.org/article/8019d712523d4708afa02fd46cc2e356
Autor:
Thomas Kolbe, Gottfried Brem, Jo Poulton, Iain G. Johnston, Thomas Rülicke, Joerg P. Burgstaller, Vitezslav Havlicek, Nick S. Jones
Publikováno v:
eLife
eLife, Vol 4 (2015)
eLife, Vol 4 (2015)
Dangerous damage to mitochondrial DNA (mtDNA) can be ameliorated during mammalian development through a highly debated mechanism called the mtDNA bottleneck. Uncertainty surrounding this process limits our ability to address inherited mtDNA diseases.
Autor:
Jo Poulton
Publikováno v:
European Journal of Paediatric Neurology. 2:99-103
It is important to recognize that mitochondrial diseases are systemic conditions and not confined to the nervous system. Many of them manifest neurological disease, however, and the main major features will be listed here. Although many patients fit
Autor:
Sylvia Bartlett, J F O'Rourke, Jonathan M. Gleadle, Peter J. Ratcliffe, Jo Poulton, Benjamin L. Ebert
Publikováno v:
Scopus-Elsevier
Recent studies have indicated that regulatory mechanisms underlying the oxygen-dependent expression of the haematopoietic growth factor erythropoietin are widely operative in non-erythropoietin-producing cells and are involved in the regulation of ot
Publikováno v:
Human Molecular Genetics. 2:23-30
In three patients with mitochondrial DNA duplications, there are two additional re-arranged molecules derived from mitochondrial DNA. Two forms of closed circular deletions of mitochondrial DNA have been characterised in all three patients, one being
Publikováno v:
American journal of physiology. Endocrinology and metabolism. 289(6)
A common mitochondrial (mt)DNA variant that is maternally inherited, the 16189 variant, is associated with type 2 diabetes and thinness at birth. To elucidate the association of the variant with thinness, we studied the 16189 variant in a well-charac
Autor:
Jo Poulton
Publikováno v:
Neuromuscular Disorders. 18:908-909
Publikováno v:
The Lancet. 354:2081-2082
Autor:
Kristina Casteels, David I.W. Phillips, Ken Ong, Marcus Pembrey, Jo Poulton, Holly Bendall, David B. Dunger
Publikováno v:
The Lancet. 353:1499-1500