Search Results - "Lopes‐Cendes, Iscia"

Using RNA Interference for Purinoceptor Knockdown In Vivo

Amorim, Rebeca Padrão^Aff3, Lopes Cendes, Iscia Teresinha^Aff5, da Silva Fernandes, Maria Jose^{Aff3, Aff4}

Pelegrín, Pablo^Aff2, Walker, John M.^Aff1

Population molecular genetics in Brazil: From genomic databases and research to the implementation of precision medicine

de Oliveira, Thais C.^{Aff1, Aff2}, Lopes-Cendes, Iscia^{Aff1, Aff2, IDs12687024007525_cor2}

The WHO genomics program of work for equitable implementation of human genomics for global health

Ambrosino, Elena^{Aff1, IDs4159102403225x_cor1}, Abou Tayoun, Ahmad N.^{Aff2, Aff3}, Abramowicz, Marc, Zilfalil, Bin Alwi, Boughtwood, Tiffany^{Aff6, Aff7}, Hamdi, Yosr, Hubbard, Tim^{Aff9, Aff10}, Kato, Kazuto, Lopes-Cendes, Iscia, Majumder, Partha Pratim^{Aff13, Aff14}, Mascalzoni, Deborah^{Aff15, Aff16}, Ndiaye, Rokhaya, Ramsay, Michèle, Repetto, Gabriela M., Shotelersuk, Vorasuk, Taylor, Sherry, Reeder, John C., Ross, Anna Laura

Gene expression associated with unfavorable vaginal bleeding in women using the etonogestrel subdermal contraceptive implant: a prospective study

Torelli, Flávia R., Rodrigues-Peres, Raquel M., Monteiro, Ilza, Lopes-Cendes, Iscia, Bahamondes, Luis, Juliato, Cássia R. T.^{Aff1, Aff3, IDs41598024617517_cor6}

Multimodal single-cell profiling reveals neuronal vulnerability and pathological cell states in focal cortical dysplasia

Galvão, Isabella C. ^{1, 2}, Lemoine, Manuela ^{1, 2}, Messias, Lauana A. ^{1, 2}, Araújo, Patrícia A.O.R.A. ^{1, 2}, Geraldis, Jaqueline C. ^{1, 2}, Yasuda, Clarissa L. ^{2, 3}, Alvim, Marina K.M. ^{2, 3}, Ghizoni, Enrico ^{2, 3}, Tedeschi, Helder ^{2, 3}, Cendes, Fernando ^{2, 3}, Rogerio, Fabio ^{2, 4}, Lopes-Cendes, Iscia ^{1, 2}, Veiga, Diogo F.T. ^{1, 2, 5, ∗}

Identification of microRNAs expressed in an animal model of periodontal disease and their impact on pathological processes

de Almeida, Kelly, Câmara, Priscilla, Camargo, Gabriela, Pereira, Tiago, Vieira, André, Lopes-Cendes, Iscia, Severino, Patrícia, Souto, Eliana B., Pascoal, Aislan, Pascoal, Vinicius

Multi-ancestry GWAS reveals excitotoxicity associated with outcome after ischaemic stroke

Ibanez, Laura, Heitsch, Laura, Carrera, Caty, Farias, Fabiana HG, Del Aguila, Jorge L, Dhar, Rajat, Budde, John, Bergmann, Kristy, Bradley, Joseph, Harari, Oscar, Phuah, Chia Ling, Lemmens, Robin, Viana Oliveira Souza, Alessandro A, Moniche, Francisco, Cabezas-Juan, Antonio, Arenillas, Juan Francisco, Krupinksi, Jerzy, Cullell, Natalia, Torres-Aguila, Nuria, Muiño, Elena, Cárcel-Márquez, Jara, Marti-Fabregas, Joan, Delgado-Mederos, Raquel, Marin-Bueno, Rebeca, Hornick, Alejandro, Vives-Bauza, Cristofol, Navarro, Rosa Diaz, Tur, Silvia, Jimenez, Carmen, Obach, Victor, Segura, Tomas, Serrano-Heras, Gemma, Chung, Jong Won, Roquer, Jaume, Soriano-Tarraga, Carol, Giralt-Steinhauer, Eva, Mola-Caminal, Marina, Pera, Joanna, Lapicka-Bodzioch, Katarzyna, Derbisz, Justyna, Davalos, Antoni, Lopez-Cancio, Elena, Muñoz, Lucia, Tatlisumak, Turgut, Molina, Carlos, Ribo, Marc, Bustamante, Alejandro, Sobrino, Tomas, Castillo-Sanchez, Jose, Campos, Francisco, Rodriguez-Castro, Emilio, Arias-Rivas, Susana, Rodríguez-Yáñez, Manuel, Herbosa, Christina, Ford, Andria L, Gutierrez-Romero, Alonso, Uribe-Pacheco, Rodrigo, Arauz, Antonio, Lopes-Cendes, Iscia, Lowenkopf, Theodore, Barboza, Miguel A, Amini, Hajar, Stamova, Boryana, Ander, Bradley P, Sharp, Frank R, Kim, Gyeong Moon, Bang, Oh Young, Jimenez-Conde, Jordi, Slowik, Agnieszka, Stribian, Daniel, Tsai, Ellen A, Burkly, Linda C, Montaner, Joan, Fernandez-Cadenas, Israel, Lee, Jin Moo, Cruchaga, Carlos

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Junctional instability in neuroepithelium and network hyperexcitability in a focal cortical dysplasia human model

Avansini, Simoni H, Puppo, Francesca, Adams, Jason W, Vieira, Andre S, Coan, Ana C, Rogerio, Fabio, Torres, Fabio R, Araújo, Patricia AOR, Martin, Mariana, Montenegro, Maria A, Yasuda, Clarissa L, Tedeschi, Helder, Ghizoni, Enrico, França, Andréa FEC, Alvim, Marina KM, Athié, Maria C, Rocha, Cristiane S, Almeida, Vanessa S, Dias, Elayne V, Delay, Lauriane, Molina, Elsa, Yaksh, Tony L, Cendes, Fernando, Lopes Cendes, Iscia, Muotri, Alysson R

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Expression of concern for global biomedical research by the human genome organization (HUGO)

Hamosh, Ada^{Aff1, IDs40246025007554_cor1}, Arzuaga, Fabiana, B. Avraham, Karen, Bin Alwi, Zilfalil, Bowcock, Anne, Burn, Sir John, Carninci, Piero, Dandara, Collet, Lopes-Cendes, Iscia, Mutesa, Leon, P. Majumder, Partha, K.V. Reichardt, Juergen^Aff1, A. Veltman, Joris

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Predictors of genetic diagnosis in individuals with developmental and epileptic encephalopathies

Luiza Benevides, Maria, de Moraes, Helena T., Granados, Diana M.M., Bonadia, Luciana C., Sauma, Letícia, Augusta Montenegro, Maria, Guerreiro, Marilisa M., Lopes-Cendes, Íscia, Carolina Coan, Ana

Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations

Stevelink, Remi, Luykx, Jurjen J, Lin, Bochao D, Leu, Costin, Lal, Dennis, Smith, Alexander W, Schijven, Dick, Carpay, Johannes A, Rademaker, Koen, Baldez, Roiza A Rodrigues, Devinsky, Orrin, Braun, Kees PJ, Jansen, Floor E, Smit, Dirk JA, Koeleman, Bobby PC, Abou‐Khalil, Bassel, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Balding, David J, Bast, Thomas, Baum, Larry, Becker, Albert J, Becker, Felicitas, Berghuis, Bianca, Berkovic, Samuel F, Boysen, Katja E, Bradfield, Jonathan P, Brody, Lawrence C, Buono, Russell J, Campbell, Ellen, Cascino, Gregory D, Catarino, Claudia B, Cavalleri, Gianpiero L, Cherny, Stacey S, Chinthapalli, Krishna, Coffey, Alison J, Compston, Alastair, Coppola, Antonietta, Cossette, Patrick, Craig, John J, de Haan, Gerrit‐Jan, De Jonghe, Peter, de Kovel, Carolien GF, Delanty, Norman, Depondt, Chantal, Dlugos, Dennis J, Doherty, Colin P, Elger, Christian E, Eriksson, Johan G, Ferraro, Thomas N, Feucht, Martha, Francis, Ben, Franke, Andre, French, Jacqueline A, Freytag, Saskia, Gaus, Verena, Geller, Eric B, Gieger, Christian, Glauser, Tracy, Glynn, Simon, Goldstein, David B, Gui, Hongsheng, Guo, Youling, Haas, Kevin F, Hakonarson, Hakon, Hallmann, Kerstin, Haut, Sheryl, Heinzen, Erin L, Helbig, Ingo, Hengsbach, Christian, Hjalgrim, Helle, Iacomino, Michele, Ingason, Andrés, Jamnadas‐Khoda, Jennifer, Johnson, Michael R, Kälviäinen, Reetta, Kantanen, Anne‐Mari, Kasperavičiūte, Dalia, Trenite, Dorothee Kasteleijn‐Nolst, Kirsch, Heidi E, Knowlton, Robert C, Krause, Roland, Krenn, Martin, Kunz, Wolfram S, Kuzniecky, Ruben, Kwan, Patrick, Lau, Yu‐Lung, Lehesjoki, Anna‐Elina, Lerche, Holger, Lieb, Wolfgang, Lindhout, Dick, Lo, Warren D, Lopes‐Cendes, Iscia, Lowenstein, Daniel H, Malovini, Alberto, Marson, Anthony G, Mayer, Thomas, McCormack, Mark, Mills, James L

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Identifying cellular markers of focal cortical dysplasia type II with cell-type deconvolution and single-cell signatures

Galvão, Isabella C.^{Aff1, Aff5}, Kandratavicius, Ludmyla^{Aff2, Aff5}, Messias, Lauana A.^{Aff1, Aff5}, Athié, Maria C. P.^{Aff1, Aff5}, Assis-Mendonça, Guilherme R.^{Aff2, Aff5}, Alvim, Marina K. M.^{Aff3, Aff5}, Ghizoni, Enrico^{Aff3, Aff5}, Tedeschi, Helder^{Aff3, Aff5}, Yasuda, Clarissa L.^{Aff3, Aff5}, Cendes, Fernando^{Aff3, Aff5}, Vieira, André S.^{Aff4, Aff5}, Rogerio, Fabio^{Aff2, Aff5}, Lopes-Cendes, Iscia^{Aff1, Aff5}, Veiga, Diogo F. T.^{Aff1, Aff5, IDs41598023402403_cor14}

The genetic architecture of the human cerebral cortex

Grasby, Katrina L, Jahanshad, Neda, Painter, Jodie N, Colodro-Conde, Lucía, Bralten, Janita, Hibar, Derrek P, Lind, Penelope A, Pizzagalli, Fabrizio, Ching, Christopher RK, McMahon, Mary Agnes B, Shatokhina, Natalia, Zsembik, Leo CP, Thomopoulos, Sophia I, Zhu, Alyssa H, Strike, Lachlan T, Agartz, Ingrid, Alhusaini, Saud, Almeida, Marcio AA, Alnæs, Dag, Amlien, Inge K, Andersson, Micael, Ard, Tyler, Armstrong, Nicola J, Ashley-Koch, Allison, Atkins, Joshua R, Bernard, Manon, Brouwer, Rachel M, Buimer, Elizabeth EL, Bülow, Robin, Bürger, Christian, Cannon, Dara M, Chakravarty, Mallar, Chen, Qiang, Cheung, Joshua W, Couvy-Duchesne, Baptiste, Dale, Anders M, Dalvie, Shareefa, de Araujo, Tânia K, de Zubicaray, Greig I, de Zwarte, Sonja MC, Braber, Anouk den, Doan, Nhat Trung, Dohm, Katharina, Ehrlich, Stefan, Engelbrecht, Hannah-Ruth, Erk, Susanne, Fan, Chun Chieh, Fedko, Iryna O, Foley, Sonya F, Ford, Judith M, Fukunaga, Masaki, Garrett, Melanie E, Ge, Tian, Giddaluru, Sudheer, Goldman, Aaron L, Green, Melissa J, Groenewold, Nynke A, Grotegerd, Dominik, Gurholt, Tiril P, Gutman, Boris A, Hansell, Narelle K, Harris, Mathew A, Harrison, Marc B, Haswell, Courtney C, Hauser, Michael, Herms, Stefan, Heslenfeld, Dirk J, Ho, New Fei, Hoehn, David, Hoffmann, Per, Holleran, Laurena, Hoogman, Martine, Hottenga, Jouke-Jan, Ikeda, Masashi, Janowitz, Deborah, Jansen, Iris E, Jia, Tianye, Jockwitz, Christiane, Kanai, Ryota, Karama, Sherif, Kasperaviciute, Dalia, Kaufmann, Tobias, Kelly, Sinead, Kikuchi, Masataka, Klein, Marieke, Knapp, Michael, Knodt, Annchen R, Krämer, Bernd, Lam, Max, Lancaster, Thomas M, Lee, Phil H, Lett, Tristram A, Lewis, Lindsay B, Lopes-Cendes, Iscia, Luciano, Michelle, Macciardi, Fabio, Marquand, Andre F, Mathias, Samuel R, Melzer, Tracy R, Milaneschi, Yuri

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The transcriptome of rat hippocampal subfields

Machado, João P.D., Athie, Maria C.P., Matos, Alexandre H.B., Lopes-Cendes, Iscia, Vieira, André.S.

Interferon-beta induces major histocompatibility complex of class I (MHC-I) expression and a proinflammatory phenotype in cultivated human astrocytes

Ignarro, Raffaela Silvestre, Bombeiro, André Luis, Chiarotto, Gabriela Bortolança, Cartarozzi, Luciana Politti, Coser, Lilian de Oliveira, Ghizoni, Enrico, Tedeschi, Helder, Cendes, Fernando, Lopes-Cendes, Iscia, Rogerio, Fabio, Oliveira, Alexandre Leite Rodrigues de

Epigenetic genes and epilepsy — emerging mechanisms and clinical applications

Van Loo, Karen M. J.^{Aff1, Aff2}, Carvill, Gemma L., Becker, Albert J., Conboy, Karen^{Aff5, Aff6}, Goldman, Alica M., Kobow, Katja, Lopes-Cendes, Iscia, Reid, Christopher A., van Vliet, Erwin A.^{Aff11, Aff12}, Henshall, David C.^{Aff5, Aff6, IDs4158202200693y_cor10}

New avenues in molecular genetics for the diagnosis and application of therapeutics to the epilepsies

Magalhães, Pedro H.M., Moraes, Helena T., Athie, Maria C.P., Secolin, Rodrigo, Lopes-Cendes, Iscia

Multi-omics in mesial temporal lobe epilepsy with hippocampal sclerosis: Clues into the underlying mechanisms leading to disease

Bruxel, Estela M., Bruno, Danielle C.F., do Canto, Amanda M., Geraldis, Jaqueline C., Godoi, Alexandre B, Martin, Mariana, Lopes-Cendes, Iscia

Revisiting the clinical impact of variants in EFHC1 in patients with different phenotypes of genetic generalized epilepsy

Gonsales, Marina C., Ribeiro, Patrícia A.O., Betting, Luiz E., Alvim, Marina K.M., Guerreiro, Carlos M., Yasuda, Clarissa L., Gitaí, Daniel L.G., Cendes, Fernando, Lopes-Cendes, Iscia