Sirt1-PPARS Cross-Talk in Complex Metabolic Diseases and Inherited Disorders of the One Carbon Metabolism

por Kosgei, Viola J., Coelho, David, Guéant-Rodriguez, Rosa-Maria, Guéant, Jean-Louis
Publicado 2020

Glycine Receptor Activation Impairs ATP-Induced Calcium Transients in Cultured Cortical Astrocytes

por Morais, Tatiana P., Coelho, David, Vaz, Sandra H., Sebastião, Ana M., Valente, Cláudia A.
Publicado 2018

Brain Susceptibility to Methyl Donor Deficiency: From Fetal Programming to Aging Outcome in Rats

por Hassan, Ziad, Coelho, David, Kokten, Tunay, Alberto, Jean-Marc, Umoret, Rémy, Daval, Jean-Luc, Guéant, Jean-Louis, Bossenmeyer-Pourié, Carine, Pourié, Grégory
Publicado 2019

Cognitive Impairment Is Associated with AMPAR Glutamatergic Dysfunction in a Mouse Model of Neuronal Methionine Synthase Deficiency

por Hassan, Ziad, Coelho, David, Bossenmeyer-Pourié, Carine, Matmat, Karim, Arnold, Carole, Savladori, Aurélie, Alberto, Jean-Marc, Umoret, Rémy, Guéant, Jean-Louis, Pourié, Grégory
Publicado 2023

Management of Coronavirus Disease 2019 Patients With Lung Cancer: Experience From a Thoracic Oncology Center

por Coelho, David Barros, Santos, Vanessa, Araújo, David, Bastos, Hélder Novais, Magalhães, Adriana, Hespanhol, Venceslau, Queiroga, Henrique, Cruz-Martins, Natália, Fernandes, Maria Gabriela O.
Publicado 2021

Effects of Toxoplasma gondii infection on cognition, symptoms, and response to digital cognitive training in schizophrenia

por Guimarães, Anna Luiza, Richer Araujo Coelho, David, Scoriels, Linda, Mambrini, Juliana, Ribeiro do Valle Antonelli, Lis, Henriques, Priscilla, Teixeira-Carvalho, Andréa, Assis Martins Filho, Olindo, Mineo, José, Bahia-Oliveira, Lilian, Panizzutti, Rogério
Publicado 2022

Author Correction: Effects of Toxoplasma gondii infection on cognition, symptoms, and response to digital cognitive training in schizophrenia

por Guimarães, Anna Luiza, Coelho, David Richer Araujo, Scoriels, Linda, Mambrini, Juliana, do Valle Antonelli, Lis Ribeiro, Henriques, Priscilla, Teixeira-Carvalho, Andréa, Martins Filho, Olindo Assis, Mineo, José, Bahia-Oliveira, Lilian, Panizzutti, Rogério
Publicado 2022

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

Traditional pipe smoking ( xanduca ) and respiratory function in the Fulni-ô indigenous people, Brazil: Project of Atherosclerosis among Indigenous Populations (PAI) study

por Pereira, Vanessa Cardoso, Coelho, David Lopes Lima Cavalcanti, dos Santos, Juracy Marques, Armstrong, Dinani Matoso Fialho de Oliveira, Patriota, Pedro Vinícius Amorim de Medeiros, Lima, João Augusto Costa, Cruz, Álvaro Augusto, do Carmo, Rodrigo Feliciano, de Souza, Carlos Dornels Freire, Armstrong, Anderson da Costa
Publicado 2022

Dose-dependent effects of siRNA-mediated inhibition of SCAP on PCSK9, LDLR, and plasma lipids in mouse and rhesus monkey

por Jensen, Kristian K., Tadin-Strapps, Marija, Wang, Sheng-ping, Hubert, James, Kan, Yanqing, Ma, Yong, McLaren, David G., Previs, Stephen F., Herath, Kithsiri B., Mahsut, Ablatt, Liaw, Andy, Wang, Shubing, Stout, Steven J., Keohan, CarolAnn, Forrest, Gail, Coelho, David, Yendluri, Satya, Williams, Stephanie, Koser, Martin, Bartz, Steven, Akinsanya, Karen O., Pinto, Shirly
Publicado 2016

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