Organic Pollutants in Water von Wegman, Ronald C. C., Melis, Peter H. A. M., Josefsson, Björn

Volltext

Organic Pollutants in Water von Wegman, Ronald C. C., Melis, Peter H. A. M., Josefsson, Björn

Volltext

Energy deficit in parvalbumin neurons leads to circuit dysfunction, impaired sensory gating and social disability von Inan, Melis, Zhao, Mingrui, Manuszak, Monica, Karakaya, Cansu, Rajadhyaksha, Anjali, Pickel, Virginia M, Schwartz, Theodore H, Goldstein, Peter A, Manfredi, Giovanni

Volltext

The influence of age on health valuations: the older olds prefer functional independence while the younger olds prefer less morbidity von Hofman, Cynthia S, Makai, Peter, Boter, Han, Buurman, Bianca M, de Craen, Anton J, Olde Rikkert, Marcel G M, Donders, Rogier, Melis, René J F

Volltext

Stillbirths: rates, risk factors, and acceleration towards 2030 von Lawn, Joy E, Prof, Blencowe, Hannah, MRCPCH, Waiswa, Peter, PhD, Amouzou, Agbessi, PhD, Mathers, Colin, PhD, Hogan, Dan, PhD, Flenady, Vicki, PhD, Frøen, J Frederik, PhD, Qureshi, Zeshan U, BM, Calderwood, Claire, BM, Shiekh, Suhail, MSc, Jassir, Fiorella Bianchi, MSc, You, Danzhen, PhD, McClure, Elizabeth M, PhD, Mathai, Matthews, PhD, Cousens, Simon, Prof

Volltext

Evaluation of an eHealth intervention in chronic care for frail older people: why adherence is the first target von Makai, Peter, Perry, Marieke, Robben, Sarah H M, Schers, Henk J, Heinen, Maud M, Olde Rikkert, Marcel G M, Melis, René F

Volltext

Rivaroxaban or aspirin for patent foramen ovale and embolic stroke of undetermined source: a prespecified subgroup analysis from the NAVIGATE ESUS trial von Lutsep, Helmi, Messé, Steven R, Nedeltechev, Krassen, Connolly, Stuart J, Anderson, C, Angel Saredo, G, Angels Font, M, Anticoli, S, Bacellar, A, Bardutzky, J, Bazan, R, Boos, L, Brouns, R, Carek, M, Chen, Z, Clark, W, Colakoglu, S, Csiba, L, Csontos, K, Cui, L, Dai, C, Dario Toledo, W, Del Giudice, A, Ehrlich, S, Epinat, M, Eren, F, Escribano, B, Ferencova, K, Frick, M, Gabriel, M, Gallina, A, Gasecki, D, Gasiorek, K, Georg Haeusler, K, Guiraudg, V, Hassan, A, Hatzitolios, A, Hermans, S, Hernandez, J, Hobeanu, MC, Hobson, B, Hon, P, Huang, D, Ioli, P, Jing, P, Judit Szabo, K, Jura, R, Kasner, SE, Kaur, S, Kemlink, D, Kosarz-Lanczek, K, Lago, A, Lajos, B, Lambeck, J, Landolfi, A, Li, J, Liang, Z, Linna, M, Ma, H, Machado, M, Mangas Guijarro, M, Manios, E, Maria Greco, L, Marta Moreno, J, Marti-Fabregas, J, Mayasi, Y, Moniche, F, Morton, M, Mudhar, O, Ng, K, Nishino, S, Patel, N, Pereira, L, Ribeiro, J, Rizzato, B, Sawicka, M, Seynaeve, L, Silva, P, Silva, Y, Slonkova, J, Stamatelopoulos, K, Takamatsu, K, Tamayo, A, Tejada Garcia, J, Tokunaga, K, Tropepi, D, Tryambake, D, Varga, Z, Vasko, P, Verocai, V, Wach-Klink, A, Weng, G, Werner, P, Wolff, V, Yalo, B, Yamada, T, Yamasaki, M, Yang, X, Yee Lam, M, Zhou, L

Volltext

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene von Kenna, Kevin P., Chia, Ruth, Dominov, Janice A., Nalls, Mike A., van Vugt, Joke J.F.A., Simone, Isabella, Caredda, Carla, Milia, Antonio, Floris, Gianluca, Caponnetto, Claudia, Mandich, Paola, Mora, Gabriele, Sideri, Riccardo, Penco, Silvana, Mandrioli, Jessica, Trojsi, Francesca, Ticca, Anna, Ortu, Enzo, Pugliatti, Maura, Benigni, Michele, Brunetti, Maura, Marrali, Giuseppe, Riva, Nilo, Conforti, Francesca L., Messina, Sonia, D’Alfonso, Sandra, Baloh, Robert H., Penny, Michelle, Moreno, Cristiane de Araujo Martins, Chung, Wendy K., Cirulli, Elizabeth T., Harris, Tim, Krueger, Brian J., Lasseigne, Brittany N., McKenna-Yasek, Diane, Myers, Richard M., Pulst, Stefan M., Raphael, Alya R., Rouleau, Guy A., Sapp, Peter C., Waite, Lindsay L., Wang, Quanli, Ostrow, Lyle W., Baas, Frank, Zaitlen, Noah, Hornstein, Eran, Patsopoulos, Nikolaos A., Kaye, Julia, Wyman, Stacia, LeNail, Alexander, Baxi, Emily, LeNail, Alex, Benatar, Michael, Hussain, Sumaira, Swenson, Andrea, Jackson, Carlayne, So, Yuen, Wuu, Joanne, Silani, Vincenzo, Fogh, Isabella, Cereda, Cristina, Ceroni, Mauro, Mazzini, Letizia, Maderna, Luca, Sorarù, Gianni, Bernard, Emilien, Laaksovirta, Hannu, McKenna-Yasek, Diane, Asress, Seneshaw, Al-Sarraj, Safa, Scholz, Sonja W., MacGowan, Daniel J.L., Kirby, Janine, Pioro, Erik P., Pamphlett, Roger, Dunckley, Travis L., Troncoso, Juan C., Moisse, Matthieu, Drory, Vivian E., Turner, Martin R., Blair, Ian P., de Carvalho, Mamede, Hide, Winston, Glass, Jonathan, Mill, Jonathan, Newhouse, Stephen, Pulit, Sara, Robberecht, Wim, Shaw, Pamela, van den Berg, Leonard, Williams, Kelly L., Zatz, Mayana, Rothstein, Jeffrey D., Simmons, Zachary, Van Damme, Philip, Sabatelli, Mario, Trojanowski, John Q., Brown, Robert H., Veldink, Jan H., Tienari, Pentti

Volltext

Interorgan amino acid exchange in humans: consequences for arginine and citrulline metabolism von Poll, Marcel CG van de, Siroen, Michiel PC, Leeuwen, Paul AM van, Soeters, Peter B, Melis, Gerdien C, Boelens, Petra G, Deutz, Nicolaas EP, Dejong, Cornelis HC

Volltext

Group VII Ethylene Response Factor diversification and regulation in four species from flood‐prone environments von VEEN, HANS, AKMAN, MELIS, JAMAR, DIAAN C. L, VREUGDENHIL, DICK, KOOIKER, MAARTEN, TIENDEREN, PETER, VOESENEK, LAURENTIUS A. C. J, SCHRANZ, M. ERIC, SASIDHARAN, RASHMI

Volltext

Signatures of TOP1 transcription-associated mutagenesis in cancer and germline von Reijns, Martin A. M., Parry, David A., Williams, Thomas C., Nadeu, Ferran, Hindshaw, Rebecca L., Rios Szwed, Diana O., Nicholson, Michael D., Carroll, Paula, Boyle, Shelagh, Royo, Romina, Cornish, Alex J., Xiang, Hang, Ridout, Kate, Schuh, Anna, Aden, Konrad, Palles, Claire, Campo, Elias, Stankovic, Tatjana, Taylor, Martin S., Jackson, Andrew P.

Volltext

Ulipristal Acetate versus Leuprolide Acetate for Uterine Fibroids von Donnez, Jacques, Tomaszewski, Janusz, Vázquez, Francisco, Bouchard, Philippe, Lemieszczuk, Boguslav, Baró, Francesco, Nouri, Kazem, Selvaggi, Luigi, Sodowski, Krzysztof, Bestel, Elke, Terrill, Paul, Osterloh, Ian, Loumaye, Ernest

Volltext

Driving slow motorised vehicles with visual impairment-A simulator study von Cordes, Christina, Heutink, Joost, Brookhuis, Karel A., Brouwer, Wiebo H., Melis-Dankers, Bart J.M.

Volltext

An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy von Pagnamenta, Alistair T, Kaiyrzhanov, Rauan, Zou, Yaqun, Da'as, Sahar I, Maroofian, Reza, Donkervoort, Sandra, Dominik, Natalia, Lauffer, Marlen, Ferla, Matteo P, Orioli, Andrea, Giess, Adam, Tucci, Arianna, Beetz, Christian, Sedghi, Maryam, Ansari, Behnaz, Barresi, Rita, Basiri, Keivan, Cortese, Andrea, Elgar, Greg, Fernandez-Garcia, Miguel A, Yip, Janice, Foley, A Reghan, Gutowski, Nicholas, Jungbluth, Heinz, Lassche, Saskia, Lavin, Tim, Marcelis, Carlo, Marks, Peter, Marini-Bettolo, Chiara, Medne, Livija, Moslemi, Ali-Reza, Sarkozy, Anna, Reilly, Mary M, Muntoni, Francesco, Millan, Francisca, Muraresku, Colleen C, Need, Anna C, Nemeth, Andrea H, Neuhaus, Sarah B, Norwood, Fiona, O'Donnell, Marie, O'Driscoll, Mary, Rankin, Julia, Yum, Sabrina W, Zolkipli-Cunningham, Zarazuela, Brusius, Isabell, Wunderlich, Gilbert, Karakaya, Mert, Wirth, Brunhilde, Fakhro, Khalid A, Tajsharghi, Homa, Bönnemann, Carsten G, Taylor, Jenny C, Houlden, Henry

Volltext

Root Transcript Profiling of Two Rorippa Species Reveals Gene Clusters Associated with Extreme Submergence Tolerance von Sasidharan, Rashmi, Mustroph, Angelika, Boonman, Alex, Akman, Melis, Ammerlaan, Ankie M.H., Breit, Timo, Schranz, M. Eric, Voesenek, Laurentius A.C.J., van Tienderen, Peter H.

Volltext

Widespread genomic influences on phenotype in Dravet syndrome, a ‘monogenic’ condition von Martins Custodio, Helena, Clayton, Lisa M, Bellampalli, Ravishankara, Pagni, Susanna, Silvennoinen, Katri, Caswell, Richard, Brunklaus, Andreas, Guerrini, Renzo, Koeleman, Bobby P C, Lemke, Johannes R, Møller, Rikke S, Scheffer, Ingrid E, Weckhuysen, Sarah, Zara, Federico, Zuberi, Sameer, Kuchenbaecker, Karoline, Balestrini, Simona, Mills, James D, Sisodiya, Sanjay M

Volltext

Spectrum of mutational signatures in T-cell lymphoma reveals a key role for UV radiation in cutaneous T-cell lymphoma von Jones, Christine L., Degasperi, Andrea, Grandi, Vieri, Amarante, Tauanne D., Mitchell, Tracey J., Nik-Zainal, Serena, Whittaker, Sean J.

Volltext

Which frail older patients use online health communities and why? A mixed methods process evaluation of use of the Health and Welfare portal von Makai, Peter, Perry, Marieke, Robben, Sarah H M, Schers, Henk, Heinen, Maud, Olde Rikkert, Marcel G M, Melis, René J F

Volltext

Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration von Vetro, Annalisa, Pelorosso, Cristiana, Balestrini, Simona, Masi, Alessio, Hambleton, Sophie, Argilli, Emanuela, Giubbolini, Simone, Barrick, Rebekah, Bergant, Gaber, Writzl, Karin, Bijlsma, Emilia K., Cacheiro, Pilar, Mei, Davide, Devlin, Anita, Machol, Keren, Mannaioni, Guido, Sakamoto, Masamune, Menezes, Manoj P., Courtin, Thomas, Sherr, Elliott, Parra, Riccardo, Richardson, Ruth, Roscioli, Tony, Scala, Marcello, von Stülpnagel, Celina, Smedley, Damian, Pochiero, Francesca, Ramesh, Venkateswaran, Capra, Valeria, Mancardi, Margherita, Keren, Boris, Mignot, Cyiril, Lulli, Matteo, Parks, Kendall, Griffin, Helen, Nigro, Vincenzo, Hirata, Yuko, Koichihara, Reiko, Peterlin, Borut, Maki, Ryuto, Nitta, Yohei, Ambrose, John C., Arumugam, Prabhu, Bevers, Roel, Bleda, Marta, Boustred, Christopher R., Brittain, Helen, Brown, Matthew A., Caulfield, Mark J., Chan, Georgia C., Giess, Adam, Griffin, John N., Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jackson, Rob, Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Lakey, Anna, Lopez, Javier F., Maleady-Crowe, Fiona, Minneci, Federico, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C., O’Donovan, Peter, Odhams, Chris A., Patch, Christine, Rahim, Tahrima, Rendon, Augusto, Sawant, Kushmita, Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C., Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R.A., Tucci, Arianna, Welland, Matthew J., Williams, Eleanor, Witkowska, Katarzyna, Wood, Suzanne M., Zarowiecki, Magdalena, Torella, Annalaura, Tohyama, Jun, Hamada, Keisuke, Ogata, Kazuhiro, Sugie, Atsushi, van der Smagt, Jasper J., van Gassen, Koen, Valence, Stephanie, Vittery, Emma, Malone, Stephen, Kato, Mitsuhiro, Ratto, Gian Michele, Guerrini, Renzo

Volltext

Rare variants in the sodium-dependent phosphate transporter gene SLC34A3 explain missing heritability of urinary stone disease von Sadeghi-Alavijeh, Omid, Chan, Melanie M Y, Moochhala, Shabbir H, Howles, Sarah, Gale, Daniel P, Böckenhauer, Detlef

Volltext