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)

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)

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

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)

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

Animal models of epilepsy: use and limitations

Por Kandratavicius, Ludmyla, Balista, Priscila Alves, Lopes-Aguiar, Cleiton, Ruggiero, Rafael Naime, Umeoka, Eduardo Henrique, Garcia-Cairasco, Norberto, Bueno-Junior, Lezio Soares, Leite, Joao Pereira
Publicado em 2014

Characterisation of psoriasis susceptibility locus 6 (PSORS6) in patients with early onset psoriasis and evidence for interaction with PSORS1

Por Hüffmeier, U, Lascorz, J, Becker, T, Schürmeier-Horst, F, Magener, A, Ekici, A B, Endele, S, Thiel, C T, Thoma-Uszynski, S, Mössner, R, Reich, K, Kurrat, W, Wienker, T F, Traupe, H, Reis, A
Publicado em 2009

Modulation of Phosducin-Like Protein 3 (PhLP3) Levels Promotes Cytoskeletal Remodelling in a MAPK and RhoA-Dependent Manner

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

Sleep-related hypermotor epilepsy: prevalence, impact and management strategies

Por Menghi, Veronica, Bisulli, Francesca, Tinuper, Paolo, Nobili, Lino
Publicado no Nat Sci Sleep (2018)

Ultra High-Resolution Gene Centric Genomic Structural Analysis of a Non-Syndromic Congenital Heart Defect, Tetralogy of Fallot

Por Bittel, Douglas C., Zhou, Xin-Gang, Kibiryeva, Nataliya, Fiedler, Stephanie, O’Brien, James E., Marshall, Jennifer, Yu, Shihui, Liu, Hong-Yu
Publicado em 2014