Zobrazeno 1 - 6 of 6 pro vyhledávání: '"Kuncheria, L"'
1
A Requirement for Zic2 in the Regulation of Nodal Expression Underlies the Establishment of Left-Sided Identity
Autor: Dykes, I, Szumska, D, Kuncheria, L, Puliyadi, R, Chen, C, Papanayotou, C, Lockstone, H, Dubourg, C, David, V, Schneider, J, Keane, T, Adams, D, Brown, S, Mercier, S, Odent, S, Collignon, J, Bhattacharya, S
Publikováno v: Scientific Reports
Scientific Reports, Nature Publishing Group, 2018, 8 (1), pp.10439. ⟨10.1038/s41598-018-28714-1⟩
Scientific Reports, Vol 8, Iss 1, Pp 1-16 (2018)
Scientific Reports, 2018, 8 (1), pp.10439. ⟨10.1038/s41598-018-28714-1⟩
International audience; ZIC2 mutation is known to cause holoprosencephaly (HPE). A subset of ZIC2 HPE probands harbour cardiovascular and visceral anomalies suggestive of laterality defects. 3D-imaging of novel mouse Zic2 mutants uncovers, in additio
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7147a9758ade095d6171bd85d09df50f
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01863217/document
Zobrazit plný text záznamu
3
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
4
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
5
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
6
Akademický článek
A Requirement for Zic2 in the Regulation of Nodal Expression Underlies the Establishment of Left-Sided Identity.
Autor: Dykes IM; Department of Cardiovascular Medicine, BHF Centre of Research Excellence, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom. I.M.Dykes@ljmu.ac.uk.; Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom. I.M.Dykes@ljmu.ac.uk.; School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Byrom Street, Liverpool, L3 3AF, United Kingdom. I.M.Dykes@ljmu.ac.uk., Szumska D; Department of Cardiovascular Medicine, BHF Centre of Research Excellence, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom.; Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom., Kuncheria L; Department of Cardiovascular Medicine, BHF Centre of Research Excellence, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom.; Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom., Puliyadi R; Department of Cardiovascular Medicine, BHF Centre of Research Excellence, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom.; Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom., Chen CM; Department of Cardiovascular Medicine, BHF Centre of Research Excellence, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom.; Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom., Papanayotou C; Institut Jacques Monod, UMR 7592, CNRS, Université Paris-Diderot, Sorbonne Paris Cité, 75013, Paris, France.; Center of Basic Research, Biomedical Research Foundation Academy of Athens, Athens, 11527, Greece., Lockstone H; Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom., Dubourg C; Faculté de Médecine, Institut de Génétique et Développement de Rennes, UMR 6290, Université de Rennes 1, Rennes, France.; Laboratoire de Génétique Moléculaire, CHU Rennes, Rennes, France., David V; Faculté de Médecine, Institut de Génétique et Développement de Rennes, UMR 6290, Université de Rennes 1, Rennes, France.; Laboratoire de Génétique Moléculaire, CHU Rennes, Rennes, France., Schneider JE; Department of Cardiovascular Medicine, BHF Centre of Research Excellence, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom.; Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom., Keane TM; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, United Kingdom., Adams DJ; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, United Kingdom., Brown SDM; Mammalian Genetics Unit, MRC Harwell Institute, Harwell Science and Innovation Campus, Oxfordshire, OX11 0RD, United Kingdom., Mercier S; CHU Nantes, Service de Génétique Médicale, 44093, Nantes, France., Odent S; Faculté de Médecine, Institut de Génétique et Développement de Rennes, UMR 6290, Université de Rennes 1, Rennes, France.; Service de Génétique clinique, CHU Rennes, France., Collignon J; Institut Jacques Monod, UMR 7592, CNRS, Université Paris-Diderot, Sorbonne Paris Cité, 75013, Paris, France., Bhattacharya S; Department of Cardiovascular Medicine, BHF Centre of Research Excellence, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom. sbhattac@well.ox.ac.uk.; Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, United Kingdom. sbhattac@well.ox.ac.uk.
Publikováno v: Scientific reports [Sci Rep] 2018 Jul 11; Vol. 8 (1), pp. 10439. Date of Electronic Publication: 2018 Jul 11.
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje