Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Vasileios I. Floros"'
Autor:
Vasileios I. Floros, Angela Pyle, Sabine Dietmann, Wei Wei, Walfred W. C. Tang, Naoko Irie, Brendan Payne, Antonio Capalbo, Laila Noli, Jonathan Coxhead, Gavin Hudson, Moira Crosier, Henrik Strahl, Yacoub Khalaf, Mitinori Saitou, Dusko Ilic, M. Azim Surani, Patrick F. Chinnery
Publikováno v:
Nature Cell Biology. 25:194-194
Autor:
Henrik Strahl, Patrick F. Chinnery, Gavin Hudson, Naoko Irie, Wei Wei, Dusko Ilic, Antonio Capalbo, Jonathan Coxhead, Yacoub Khalaf, Brendan A I Payne, Moira Crosier, Walfred C. W. Tang, Laila Noli, Angela Pyle, Vasileios I. Floros, M. Azim Surani, Sabine Dietmann, Mitinori Saitou
Publikováno v:
Nature cell biology. 20(2)
Mitochondrial DNA (mtDNA) mutations cause inherited diseases and are implicated in the pathogenesis of common late-onset disorders, but how they arise is not clear1,2. Here we show mtDNA mutations are present in primordial germ cells (PGCs) within he
Autor:
Mary Herbert, Dimitrios Kalleas, Rolf Jessberger, Sarah Louise Pace, Jaclyn Catharina Barel, Lisa M. Lister, Anna Kouznetsova, Louise Hyslop, Thomas B. L. Kirkwood, Abinaya Nathan, Vasileios I. Floros, Christer Höög, Yoshinori Watanabe, Caroline Adelfalk
Publikováno v:
Current Biology. 20:1511-1521
Summary Background The growing trend for women to postpone childbearing has resulted in a dramatic increase in the incidence of trisomic pregnancies. Maternal age-related miscarriage and birth defects are predominantly a consequence of chromosome seg
Autor:
Vasileios I. Floros, Laila Noli, Wei Wei, Sabine Dietmann, Angela Pyle, M. Azim Surani, Henrik Strahl, Mitinori Saitou, Gavin Hudson, Yacoub Khalaf, Moira Crosier, Patrick F. Chinnery, Jonathan Coxhead, Naoko Irie, Antonio Capalbo, Brendan A I Payne, Dusko Ilic, Walfred W. C. Tang
Publikováno v:
Nature Cell Biology. 20:991-991
In the version of this Letter originally published, an author error led to the affiliations for Brendan Payne, Jonathan Coxhead and Gavin Hudson being incorrect. The correct affiliations are: Brendan Payne: 3Wellcome Trust Centre for Mitochondrial Re
Autor:
James B. Stewart, Nils-Göran Larsson, Arnaud Mourier, Camilla Koolmeister, Lynsey M. Cree, Vasileios I. Floros, Emmanouella E. Chatzidaki, Dusanka Milenkovic, Timothy Wai, David C. Samuels, Erik Hagström, Rudolph J. Wiesner, Patrick F. Chinnery, Christoph Freyer
Publikováno v:
Nature Genetics
Nature Genetics, Nature Publishing Group, 2012, 44 (11), pp.1282-1285. ⟨10.1038/ng.2427⟩
Nat Genet
Nature Genetics, Nature Publishing Group, 2012, 44 (11), pp.1282-1285. ⟨10.1038/ng.2427⟩
Nat Genet
A genetic bottleneck explains the marked changes in mitochondrial DNA (mtDNA) heteroplasmy that are observed during the transmission of pathogenic mutations, but the precise timing of these changes remains controversial, and it is not clear whether s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d51c1d6eeb23dc2417a9ffcfcc5fb13c
https://hal.archives-ouvertes.fr/hal-02391255
https://hal.archives-ouvertes.fr/hal-02391255