Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Carine Bossenmeyer-Pourié"'
Autor:
Arnaud Michel, Tunay Kokten, Lynda Saber-Cherif, Rémy Umoret, Jean-Marc Alberto, Déborah Helle, Amélia Julien, Jean-Luc Daval, Jean-Louis Guéant, Carine Bossenmeyer-Pourié, Grégory Pourié
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 12, p 9847 (2023)
Vitamin B9 (folate)/B12 (cobalamin) deficiency is known to induce brain structural and/or functional retardations. In many countries, folate supplementation, targeting the most severe outcomes such as neural tube defects, is discontinued after the fi
Externí odkaz:
https://doaj.org/article/9efe715f4a9d409a80f12bae94b66aa4
Autor:
Ziad Hassan, David Coelho, Carine Bossenmeyer-Pourié, Karim Matmat, Carole Arnold, Aurélie Savladori, Jean-Marc Alberto, Rémy Umoret, Jean-Louis Guéant, Grégory Pourié
Publikováno v:
Cells, Vol 12, Iss 9, p 1267 (2023)
Impairment of one-carbon metabolism during pregnancy, either due to nutritional deficiencies in B9 or B12 vitamins or caused by specific genetic defects, is often associated with neurological defects, including cognitive dysfunction that persists eve
Externí odkaz:
https://doaj.org/article/4238e1b136d94a18b1cbbbcb39e748e3
Autor:
Grégory Pourié, Nicolas Martin, Jean-Luc Daval, Jean-Marc Alberto, Rémy Umoret, Jean-Louis Guéant, Carine Bossenmeyer-Pourié
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 21, p 8008 (2020)
A deficiency in B-vitamins is known to lead to persistent developmental defects in various organs during early life. The nervous system is particularly affected with functional retardation in infants and young adults. In addition, even if in some cas
Externí odkaz:
https://doaj.org/article/e056c57066034e4cb8777e145ea139d2
Autor:
Lynda Saber Cherif, Grégory Pourié, Andréa Geoffroy, Amélia Julien, Déborah Helle, Aurélie Robert, Rémy Umoret, Jean-Louis Guéant, Carine Bossenmeyer-Pourié, Jean-Luc Daval
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 20, p 5097 (2019)
The micronutrients vitamins B9 and B12 act as methyl donors in the one-carbon metabolism involved in transmethylation reactions which critically influence epigenetic mechanisms and gene expression. Both vitamins are essential for proper development,
Externí odkaz:
https://doaj.org/article/a298879af85848cab69fa53df1bd5c84
Autor:
Andréa Geoffroy, Lynda Saber-Cherif, Grégory Pourié, Déborah Helle, Rémy Umoret, Jean-Louis Guéant, Carine Bossenmeyer-Pourié, Jean-Luc Daval
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 4, p 973 (2019)
Vitamins B9 (folate) and B12 act as methyl donors in the one-carbon metabolism which influences epigenetic mechanisms. We previously showed that an embryofetal deficiency of vitamins B9 and B12 in the rat increased brain expression of let-7a and miR-
Externí odkaz:
https://doaj.org/article/5fe5a75927484361a91720aeaac2e301
Autor:
Nicolas Martin, Carine Bossenmeyer-Pourié, Violette Koziel, Rozat Jazi, Sandra Audonnet, Paul Vert, Jean-Louis Guéant, Jean-Luc Daval, Grégory Pourié
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e48828 (2012)
Whereas brief acute or intermittent episodes of hypoxia have been shown to exert a protective role in the central nervous system and to stimulate neurogenesis, other studies suggest that early hypoxia may constitute a risk factor that influences the
Externí odkaz:
https://doaj.org/article/30b7fb9436494b3cbaa7c77f26aafba7
Autor:
Armand Hocquel, Jean-Marie Ravel, Laetitia Lambert, Céline Bonnet, Guillaume Banneau, Bophara Kol, Laurène Tissier, Lucie Hopes, Mylène Meyer, Céline Dillier, Maud Michaud, Arnaud Lardin, Anne-Laure Kaminsky, Emmanuelle Schmitt, Liang Liao, François Zhu, Bronner Myriam, Carine Bossenmeyer-Pourié, Antoine Verger, Mathilde Renaud
Publikováno v:
neurogenetics. 23:241-255
Autor:
Arnaud Michel, Tunay Kokten, Lynda Saber Cherif, Rémy Umoret, Jean-Marc Alberto, Déborah Helle, Amélia Julien, Daval Jean-Luc, Jean-Louis Guéant, Carine Bossenmeyer-Pourié, Grégory Pourié
Vitamin B9(folate)/B12 deficiency is known to induce brain structural and/or functional retardations. Besides neural tube defects in case of major consequences, several mild deregulations also lead to deleterious effect after birth, and folate supple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bd2ead99839e571261848329a625435
https://doi.org/10.20944/preprints202304.0383.v1
https://doi.org/10.20944/preprints202304.0383.v1
Autor:
Jean-Louis Guéant, Lise Larrieu, Louise Tyvaert, Mehdi Benkirane, Jean-Marie Ravel, Nadège Calmels, Fabienne Ory-Magne, Philippe Casenave, Laetitia Lambert, Nathalie Drouot, Mathieu Anheim, Christine Tranchant, Morgane Pointaux, Guillaume Pisché, Yosra Halleb, Cecilia Marelli, Claire Ewenczyk, Carine Bossenmeyer-Pourié, Bruno Leheup, Mathilde Renaud, Abderrahim Oussalah, Michel Koenig, Annabelle Chaussenot, Solène Frismand, François Tison, Céline Bonnet, Jamel Chelly, Claire Lecocq
Publikováno v:
Journal of Neurology
Journal of Neurology, Springer Verlag, 2021, 268 (5), pp.1927-1937. ⟨10.1007/s00415-020-10348-x⟩
Journal of Neurology, Springer Verlag, 2021, 268 (5), pp.1927-1937. ⟨10.1007/s00415-020-10348-x⟩
STUB1 has been first associated with autosomal recessive (SCAR16, MIM# 615768) and later with dominant forms of ataxia (SCA48, MIM# 618093). Pathogenic variations in STUB1 are now considered a frequent cause of cerebellar ataxia. We aimed to improve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::637efe2c78a1cf1f9d85c19d40ecb50f
https://hal.archives-ouvertes.fr/hal-03359686
https://hal.archives-ouvertes.fr/hal-03359686
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