CombFunc: predicting protein function using heterogeneous data sources

Por Wass, Mark N., Barton, Geraint, Sternberg, Michael J. E.
Publicado em 2012

Describing the genetic architecture of epilepsy through heritability analysis

Por Speed, Doug, O’Brien, Terence J., Palotie, Aarno, Shkura, Kirill, Marson, Anthony G., Balding, David J., Johnson, Michael R.
Publicado em 2014

Depdc5 knockdown causes mTOR‐dependent motor hyperactivity in zebrafish

Por de Calbiac, Hortense, Dabacan, Adriana, Marsan, Elise, Tostivint, Hervé, Devienne, Gabrielle, Ishida, Saeko, Leguern, Eric, Baulac, Stéphanie, Muresan, Raul C., Kabashi, Edor, Ciura, Sorana
Publicado no Ann Clin Transl Neurol (2018)

Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies

Por Pippucci, Tommaso, Licchetta, Laura, Baldassari, Sara, Marconi, Caterina, De Luise, Monica, Myers, Candace, Nardi, Elena, Provini, Federica, Cameli, Cinzia, Minardi, Raffaella, Bacchelli, Elena, Giordano, Lucio, Crichiutti, Giovanni, d'Orsi, Giuseppe, Seri, Marco, Gasparre, Giuseppe, Mefford, Heather C., Tinuper, Paolo, Bisulli, Francesca
Publicado no Ann Clin Transl Neurol (2019)

Epistatic partners of neurogenic genes modulate Drosophila olfactory behavior

Por He, X., Zhou, S., St. Armour, G. E., Mackay, T. F. C., Anholt, R. R. H.
Publicado no Genes Brain Behav (2016)

Therapeutic potential of Focal Adhesion Kinase inhibition in small cell lung cancer

Por Nana, Frank Aboubakar, Lecocq, Marylène, Ladjemi, Maha Zohra, Detry, Bruno, Dupasquier, Sébastien, Feron, Olivier, Massion, Pierre P., Sibille, Yves, Pilette, Charles, Ocak, Sebahat
Publicado no Mol Cancer Ther (2018)

New insights into the genetics of glioblastoma multiforme by familial exome sequencing

Por Backes, Christina, Harz, Christian, Fischer, Ulrike, Schmitt, Jana, Ludwig, Nicole, Petersen, Britt-Sabina, Mueller, Sabine C., Kim, Yoo-Jin, Wolf, Nadine M., Katus, Hugo A., Meder, Benjamin, Furtwängler, Rhoikos, Franke, Andre, Bohle, Rainer, Henn, Wolfram, Graf, Norbert, Keller, Andreas, Meese, Eckart
Publicado no Oncotarget (2014)

Modulation of phosducin-like protein 3 (PhLP3) levels promotes cytoskeletal remodelling in a MAPK and RhoA-dependent manner.

Por Nandini V L Hayes, Lyne Jossé, C Mark Smales, Martin J Carden
Publicado em 2011-01-01

Loss of the candidate tumor suppressor ZEB1 (TCF8, ZFHX1A) in Sézary syndrome

Por Caprini, Elisabetta, Bresin, Antonella, Cristofoletti, Cristina, Helmer Citterich, Mauro, Tocco, Valeria, Scala, Enrico, Monopoli, Alessandro, Benucci, Roberto, Narducci, Maria Grazia, Russo, Giandomenico
Publicado no Cell Death Dis (2018)

Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses

Por Addis, Laura, Sproviero, William, Thomas, Sanjeev V, Caraballo, Roberto H, Newhouse, Stephen J, Gomez, Kumudini, Hughes, Elaine, Kinali, Maria, McCormick, David, Hannan, Siobhan, Cossu, Silvia, Taylor, Jacqueline, Akman, Cigdem I, Wolf, Steven M, Mandelbaum, David E, Gupta, Rajesh, van der Spek, Rick A, Pruna, Dario, Pal, Deb K
Publicado no J Med Genet (2018)

HIV and chronic kidney disease

Por Naicker, Saraladevi, Rahmania, Sadaf, Kopp, Jeffrey B.
Publicado no Clin Nephrol (2015)

Genetic association analyses highlight biological pathways underlying mitral valve prolapse

Por Dina, Christian, Bouatia-Naji, Nabila, Tucker, Nathan, Delling, Francesca N., Toomer, Katelynn, Durst, Ronen, Perrocheau, Maelle, Fernandez-Friera, Leticia, Solis, Jorge, Le Tourneau, Thierry, Chen, Ming-Huei, Probst, Vincent, Bosse, Yohan, Pibarot, Philippe, Zelenika, Diana, Lathrop, Mark, Hercberg, Serge, Roussel, Ronan, Benjamin, Emelia J., Bonnet, Fabrice, Su Hao, LO, Dolmatova, Elena, Simonet, Floriane, Lecointe, Simon, Kyndt, Florence, Redon, Richard, Le Marec, Hervé, Froguel, Philippe, Ellinor, Patrick T., Vasan, Ramachandran S., Bruneval, Patrick, Norris, Russell A., Milan, David J., Slaugenhaupt, Susan A., Levine, Robert A., Schott, Jean-Jacques, Hagege, Albert A., Jeunemaitre, Xavier
Publicado no Nat Genet (2015)

Gain of FGF4 is a frequent event in KIT/PDGFRA/SDH/RAS‐P WT GIST

Por Urbini, Milena, Indio, Valentina, Tarantino, Giuseppe, Ravegnini, Gloria, Angelini, Sabrina, Nannini, Margherita, Saponara, Maristella, Santini, Donatella, Ceccarelli, Claudio, Fiorentino, Michelangelo, Vincenzi, Bruno, Fumagalli, Elena, Casali, Paolo Giovanni, Grignani, Giovanni, Pession, Andrea, Ardizzoni, Andrea, Astolfi, Annalisa, Pantaleo, Maria Abbondanza
Publicado no Genes Chromosomes Cancer (2019)

Poster Session A

Publicado no Mol Cell Proteomics (2019)

Developmental and Genetic Modulation of Arsenic Biotransformation: A Gene by Environment Interaction?

Por Meza, Mercedes, Gandolfi, A. Jay, Klimecki, Walter T.
Publicado em 2006

FOCAL EPILEPSIES: PATHOMORPHOSIS TYPES

Por M. G. Amirkhanian, A. S. Kotov, Yu. V. Eliseev, A. V. Shatalin
Publicado em 2017-12-01

Invadopodia in context

Por Bergman, Aviv, Condeelis, John S, Gligorijevic, Bojana
Publicado em 2014

RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population

Por Zhou, Sirui, Ambalavanan, Amirthagowri, Rochefort, Daniel, Xie, Pingxing, Bourassa, Cynthia V., Hince, Pascale, Dionne-Laporte, Alexandre, Spiegelman, Dan, Gan-Or, Ziv, Mirarchi, Cathy, Zaharieva, Vessela, Dupré, Nicolas, Kobayashi, Hatasu, Hitomi, Toshiaki, Harada, Kouji, Koizumi, Akio, Xiong, Lan, Dion, Patrick A., Rouleau, Guy A.
Publicado no Am J Hum Genet (2016)

Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections

Por Ye, Zhan, Vasco, Daniel A., Carter, Tonia C., Brilliant, Murray H., Schrodi, Steven J., Shukla, Sanjay K.
Publicado em 2014

Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome

Por Gerards, M, Sluiter, W, van den Bosch, B J C, de Wit, L E A, Calis, C M H, Frentzen, M, Akbari, H, Schoonderwoerd, K, Scholte, H R, Jongbloed, R J, Hendrickx, A T M, de Coo, I F M, Smeets, H J M
Publicado em 2009