Zobrazeno 1 - 4
of 4
pro vyhledávání: '"MESH: Vitamin B 12 Deficiency"'
Fetal Programming by Methyl Donor Deficiency Produces Pathological Remodeling of the Ascending Aorta
Autor:
Sébastien Blaise, Jean-Louis Guéant, Jean-Michel Camadro, Sébastien Hergalant, Laetitia Vanalderwiert, Rosa-Maria Guéant-Rodriguez, Brittany Balint, Laurent Lignières
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology
Arteriosclerosis, Thrombosis, and Vascular Biology, American Heart Association, 2021, 41 (6), pp.1928-1941. ⟨10.1161/atvbaha.120.315587⟩
Arteriosclerosis, Thrombosis, and Vascular Biology, American Heart Association, 2021, 41 (6), pp.1928-1941. ⟨10.1161/ATVBAHA.120.315587⟩
Arteriosclerosis, Thrombosis, and Vascular Biology, American Heart Association, 2021, 41 (6), pp.1928-1941. ⟨10.1161/atvbaha.120.315587⟩
Arteriosclerosis, Thrombosis, and Vascular Biology, American Heart Association, 2021, 41 (6), pp.1928-1941. ⟨10.1161/ATVBAHA.120.315587⟩
Objective: Deficiency in vitamin B12/folate (methyl donor deficiency [MDD]) produces cardiovascular outcomes during aging and fetal programming effects in newborns of MDD mothers. Whether fetal programming provokes long-term effects on aorta remains
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87b20e6604bfb390011bfd2b19b3e357
https://hal.archives-ouvertes.fr/hal-03238712
https://hal.archives-ouvertes.fr/hal-03238712
Autor:
Jean-Louis Guéant, David Coelho, François Feillet, Natacha Dreumont, Ziad Hassan, Virginie Marchand, Matthias R. Baumgartner, Abderrahim Oussalah, Jean-Michel Camadro, Justine Flayac, David S. Rosenblatt, Charif Rashka, Sébastien Hergalant
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2020, 29 (12), pp.1969-1985. ⟨10.1093/hmg/ddaa027⟩
Human Molecular Genetics, 2020, 29 (12), pp.1969-1985. ⟨10.1093/hmg/ddaa027⟩
Human Molecular Genetics, Oxford University Press (OUP), 2020, ⟨10.1093/hmg/ddaa027⟩
Human Molecular Genetics, Oxford University Press (OUP), 2020, 29 (12), pp.1969-1985. ⟨10.1093/hmg/ddaa027/5739951⟩
Human Molecular Genetics, Oxford University Press (OUP), 2020, 29 (12), pp.1969-1985. ⟨10.1093/hmg/ddaa027⟩
Human Molecular Genetics, 2020, 29 (12), pp.1969-1985. ⟨10.1093/hmg/ddaa027⟩
Human Molecular Genetics, Oxford University Press (OUP), 2020, ⟨10.1093/hmg/ddaa027⟩
Human Molecular Genetics, Oxford University Press (OUP), 2020, 29 (12), pp.1969-1985. ⟨10.1093/hmg/ddaa027/5739951⟩
International audience; Vitamin B12 or cobalamin (Cbl) metabolism can be affected by genetic defects leading to defective activity of either methylmalonyl-CoA mutase or methionine synthase or both enzymes. Patients usually present with a wide spectru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a35e86a40e26fcc1ed1e42acaa3f2b5
https://hal-cnrs.archives-ouvertes.fr/hal-03100129/document
https://hal-cnrs.archives-ouvertes.fr/hal-03100129/document
Autor:
Michael P. Conley, Kelsey B Sheehan, Jessica M Ryan, Debra J. Reid, Carla Bouwmeester, Stacy L Longo
Publikováno v:
Pharmacy Practice
Pharmacy Practice, Vol 17, Iss 3, p 1499 (2019)
Pharmacy Practice (Granada), Volume: 17, Issue: 3, Article number: 1499, Published: 25 NOV 2019
Pharmacy Practice (Granada) v.17 n.3 2019
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
instname
Pharmacy Practice, Vol 17, Iss 3, p 1499 (2019)
Pharmacy Practice (Granada), Volume: 17, Issue: 3, Article number: 1499, Published: 25 NOV 2019
Pharmacy Practice (Granada) v.17 n.3 2019
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
instname
Background: Previous studies linked metformin use to vitamin B12 deficiency and demonstrated that the prevalence of vitamin B12 monitoring remains low. Objective: This study aimed to assess the occurrence of monitoring vitamin B12 levels in a diverse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::670886f04ab1363d6fb67469155571ed
https://pubmed.ncbi.nlm.nih.gov/31592289
https://pubmed.ncbi.nlm.nih.gov/31592289
Autor:
Corinne Sagné, Horst Robenek, Azita Sharifi, Thorsten Marquardt, Mohammad R. Toliat, Martin Stucki, Tanja Wittkampf, Christian Becker, Peter Nürnberg, Frank Rutsch, Terttu Suormala, David S. Rosenblatt, Wolfgang Höhne, Matthias R. Baumgartner, Insa Buers, Brian Fowler, Susann Gailus, Isabelle R. Miousse, Gudrun Nürnberg, Bruno Gasnier
Publikováno v:
Nature genetics
Nature Genetics
Nature Genetics, Nature Publishing Group, 2009, 41 (2), pp.234-9. ⟨10.1038/ng.294⟩
Nature Genetics
Nature Genetics, Nature Publishing Group, 2009, 41 (2), pp.234-9. ⟨10.1038/ng.294⟩
International audience; Vitamin B(12) (cobalamin) is essential in animals for metabolism of branched chain amino acids and odd chain fatty acids, and for remethylation of homocysteine to methionine. In the cblF inborn error of vitamin B(12) metabolis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::719f29e3615cb91fbbb0595e20d17923