Besides Pathology: Long Non-Coding RNA in Cell and Tissue Homeostasis

por Salviano-Silva, Amanda, Lobo-Alves, Sara Cristina, de Almeida, Rodrigo Coutinho, Malheiros, Danielle, Petzl-Erler, Maria Luiza
Publicado 2018

Sparking Fire Under the Skin? Answers From the Association of Complement Genes With Pemphigus Foliaceus

por Bumiller-Bini, Valéria, Cipolla, Gabriel Adelman, de Almeida, Rodrigo Coutinho, Petzl-Erler, Maria Luiza, Augusto, Danillo Gardenal, Boldt, Angelica Beate Winter
Publicado 2018

Hyper-physiologic mechanical cues, as an osteoarthritis disease relevant environmental perturbation, cause a critical shift in set-points of methylation at transcriptionally active...

por Bloks, Niek GC, Dicks, Amanda, Harissa, Zainab, Nelissen, Rob GHH, Hajmousa, Ghazaleh, Ramos, Yolande FM, Almeida, Rodrigo Coutinho, Guilak, Farshid, Meulenbelt, Ingrid
Publicado 2023

Characterizing the secretome of licensed hiPSC-derived MSCs

por Ramos, Yolande F. M., Tertel, Tobias, Shaw, Georgina, Staubach, Simon, de Almeida, Rodrigo Coutinho, Suchiman, Eka, Kuipers, Thomas B., Mei, Hailiang, Barry, Frank, Murphy, Mary, Giebel, Bernd, Meulenbelt, Ingrid
Publicado 2022

Elucidating Epigenetic Regulation by Identifying Functional cis‐Acting Long Noncoding RNAs and Their Targets in Osteoarthritic Articular Cartilage

por van Hoolwerff, Marcella, Metselaar, Paula I., Tuerlings, Margo, Suchiman, H. Eka D., Lakenberg, Nico, Ramos, Yolande F.M., Cats, Davy, Nelissen, Rob G.H.H., Broekhuis, Demiën, Mei, Hailiang, de Almeida, Rodrigo Coutinho, Meulenbelt, Ingrid
Publicado 2020

A genetic variant in microRNA-146a is associated with sporadic breast cancer in a Southern Brazilian Population

por Brincas, Heloisa Magagnin, Augusto, Danillo G., Mathias, Carolina, Cavalli, Iglenir João, de Lima, Rubens Silveira, Kuroda, Flávia, Urban, Cícero de Andrade, Gradia, Daniela Fiori, de Oliveira, Jaqueline, de Almeida, Rodrigo Coutinho, Ribeiro, Enilze Maria de Souza Fonseca
Publicado 2020

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

por Trynka, Gosia, Hunt, Karen A, Bockett, Nicholas A, Romanos, Jihane, Mistry, Vanisha, Szperl, Agata, Bakker, Sjoerd F, Bardella, Maria Teresa, Bhaw-Rosun, Leena, Castillejo, Gemma, de la Concha, Emilio G., de Almeida, Rodrigo Coutinho, Dias, Kerith-Rae M, van Diemen, Cleo C., Dubois, Patrick CA, Duerr, Richard H., Edkins, Sarah, Franke, Lude, Fransen, Karin, Gutierrez, Javier, Heap, Graham AR, Hrdlickova, Barbara, Hunt, Sarah, Izurieta, Leticia Plaza, Izzo, Valentina, Joosten, Leo AB, Langford, Cordelia, Mazzilli, Maria Cristina, Mein, Charles A, Midah, Vandana, Mitrovic, Mitja, Mora, Barbara, Morelli, Marinita, Nutland, Sarah, Núñez, Concepción, Onengut-Gumuscu, Suna, Pearce, Kerra, Platteel, Mathieu, Polanco, Isabel, Potter, Simon, Ribes-Koninckx, Carmen, Ricaño-Ponce, Isis, Rich, Stephen S., Rybak, Anna, Santiago, José Luis, Senapati, Sabyasachi, Sood, Ajit, Szajewska, Hania, Troncone, Riccardo, Varadé, Jezabel, Wallace, Chris, Wolters, Victorien M, Zhernakova, Alexandra, Thelma, B.K., Cukrowska, Bozena, Urcelay, Elena, Bilbao, Jose Ramon, Mearin, M Luisa, Barisani, Donatella, Barrett, Jeffrey C, Plagnol, Vincent, Deloukas, Panos, Wijmenga, Cisca, van Heel, David A
Publicado 2011