Acute camptocormia induced by olanzapine: a case report

por Robert, Florence, Koenig, Martial, Robert, Aurélie, Boyer, Stéphane, Cathébras, Pascal, Camdessanché, Jean-Philippe
Publicado 2010

Methyl Donor Deficiency during Gestation and Lactation in the Rat Affects the Expression of Neuropeptides and Related Receptors in the Hypothalamus

por Saber Cherif, Lynda, Pourié, Grégory, Geoffroy, Andréa, Julien, Amélia, Helle, Déborah, Robert, Aurélie, Umoret, Rémy, Guéant, Jean-Louis, Bossenmeyer-Pourié, Carine, Daval, Jean-Luc
Publicado 2019

A transgenic mice model of retinopathy of cblG-type inherited disorder of one-carbon metabolism highlights epigenome-wide alterations related to cone photoreceptor cells developmen...

por Matmat, Karim, Conart, Jean-Baptiste, Graindorge, Paul-Henri, El Kouche, Sandra, Hassan, Ziad, Siblini, Youssef, Umoret, Rémy, Safar, Ramia, Baspinar, Okan, Robert, Aurélie, Alberto, Jean-Marc, Oussalah, Abderrahim, Coelho, David, Guéant, Jean-Louis, Guéant-Rodriguez, Rosa-Maria
Publicado 2023

Inherited disorders of cobalamin metabolism disrupt nucleocytoplasmic transport of mRNA through impaired methylation/phosphorylation of ELAVL1/HuR

por Battaglia-Hsu, Shyue-Fang, Ghemrawi, Rose, Coelho, David, Dreumont, Natacha, Mosca, Pauline, Hergalant, Sébastien, Gauchotte, Guillaume, Sequeira, Jeffrey M, Ndiongue, Mariam, Houlgatte, Rémi, Alberto, Jean-Marc, Umoret, Remy, Robert, Aurélie, Paoli, Justine, Jung, Martin, Quadros, Edward V, Guéant, Jean-Louis
Publicado 2018

A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients

por Guéant, Jean-Louis, Chéry, Céline, Oussalah, Abderrahim, Nadaf, Javad, Coelho, David, Josse, Thomas, Flayac, Justine, Robert, Aurélie, Koscinski, Isabelle, Gastin, Isabelle, Filhine-Tresarrieu, Pierre, Pupavac, Mihaela, Brebner, Alison, Watkins, David, Pastinen, Tomi, Montpetit, Alexandre, Hariri, Fadi, Tregouët, David, Raby, Benjamin A, Chung, Wendy K., Morange, Pierre-Emmanuel, Froese, D. Sean, Baumgartner, Matthias R., Benoist, Jean-François, Ficicioglu, Can, Marchand, Virginie, Motorin, Yuri, Bonnemains, Chrystèle, Feillet, François, Majewski, Jacek, Rosenblatt, David S.
Publicado 2018

Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients

por Guéant, Jean-Louis, Chéry, Céline, Oussalah, Abderrahim, Nadaf, Javad, Coelho, David, Josse, Thomas, Flayac, Justine, Robert, Aurélie, Koscinski, Isabelle, Gastin, Isabelle, Filhine-Tresarrieu, Pierre, Pupavac, Mihaela, Brebner, Alison, Watkins, David, Pastinen, Tomi, Montpetit, Alexandre, Hariri, Fadi, Tregouët, David, Raby, Benjamin A, Chung, Wendy K., Morange, Pierre-Emmanuel, Froese, D. Sean, Baumgartner, Matthias R., Benoist, Jean-François, Ficicioglu, Can, Marchand, Virginie, Motorin, Yuri, Bonnemains, Chrystèle, Feillet, François, Majewski, Jacek, Rosenblatt, David S.
Publicado 2018