CircRNAs in hematopoiesis and hematological malignancies von Bonizzato, A, Gaffo, E, te Kronnie, G, Bortoluzzi, S

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Heparan Sulfate Glycosaminoglycans Are Receptors Sufficient To Mediate the Initial Binding of Adenovirus Types 2 and 5 von Dechecchi, M C, Melotti, P, Bonizzato, A, Santacatterina, M, Chilosi, M, Cabrini, G

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Pan-cancer analysis of whole genomes von Campbell, Peter J, Getz, Gad, Korbel, Jan O, Stuart, Joshua M, Jennings, Jennifer L, Stein, Lincoln D, Perry, Marc D

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Comprehensive molecular characterization of mitochondrial genomes in human cancers von Yuan, Yuan, Ju, Young Seok, Kim, Youngwook, Li, Jun, Wang, Yumeng, Yoon, Christopher J., Yang, Yang, Martincorena, Inigo, Creighton, Chad J., Weinstein, John N., Xu, Yanxun, Han, Leng, Kim, Hyung-Lae, Nakagawa, Hidewaki, Park, Keunchil, Campbell, Peter J., Liang, Han

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Genetic tests for low- and middle-income countries: a literature review von Maltese, P E, Poplavskaia, E, Malyutkina, I, Sirocco, F, Bonizzato, A, Capodicasa, N, Nicoulina, S Y, Salmina, A, Aksutina, N, Dundar, M, Beccari, T, Cecchin, S, Bertelli, M

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A Rare Case of Emberger Syndrome Caused By a De Novo Mutation in the GATA2 Gene von Michelini, S, Cardone, M, Haag, M, Agga, O, Bruson, A, Maltese, P E, Bonizzato, A, Bertelli, M

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Divergent mutational processes distinguish hypoxic and normoxic tumours von Bhandari, Vinayak, Li, Constance H., Bristow, Robert G., Boutros, Paul C.

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LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study von Quadri, Marialuisa, Mandemakers, Wim, Grochowska, Martyna M, Masius, Roy, Geut, Hanneke, Fabrizio, Edito, Kuipers, Demy, Minneboo, Michelle, Vergouw, Leonie J M, Yonova-Doing, Ekaterina, Simons, Erik, Zhao, Tianna, Chang, Hsiu-Chen, Parchi, Piero, Correia Guedes, Leonor, Thomas, Astrid, Brouwer, Rutger W W, Heijsman, Daphne, Ingrassia, Angela M T, Calandra Buonaura, Giovanna, Sarchioto, Marianna, Vanacore, Nicola, Olgiati, Simone, Wu-Chou, Yah-Huei, Yeh, Tu-Hsueh, Boon, Agnita J W, Hoogers, Susanne E, Ghazvini, Mehrnaz, IJpma, Arne S, van IJcken, Wilfred F J, Onofrj, Marco, Barone, Paolo, Nicholl, David J, De Mari, Michele, Barbosa, Egberto, De Michele, Giuseppe, Majoor-Krakauer, Danielle, van Swieten, John C, de Jong, Frank J, Ferreira, Joaquim J, Lu, Chin-Song, Meco, Giuseppe, Cortelli, Pietro, van de Berg, Wilma D J, Bonifati, Vincenzo, Mandemakers, Wim, Boon, Agnita J.W., Rood, Janneke P.A, Vergouw, Leonie J.M., de Jong, Frank J., van Swieten, John C., Mattace-Raso, Francesco U.S., Leenders, Klaus L., Ferreira, Joaquim J., Correia Guedes, Leonor, Puschmann, Andreas, Ygland, Emil, Nilsson, Christer, Chien, Hsin F., Barbosa, Egberto, Bannach Jardim, Laura, Rieder, Carlos R.M., Chang, Hsiu-Chen, Lu, Chin-Song, Wu-Chou, Yah-Huei, Yeh, Tu-Hsueh, Tassorelli, Cristina, Pacchetti, Claudio, Riboldazzi, Giulio, Bono, Giorgio, Comi, Cristoforo, Padovani, Alessandro, Borroni, Barbara, Raudino, Francesco, Tinazzi, Michele, Ferracci, Carlo, Dalla Libera, Alessio, Abbruzzese, Giovanni, Cortelli, Pietro, Marconi, Roberto, Guidi, Marco, Onofrj, Marco, Thomas, Astrid, Vanacore, Nicola, Meco, Giuseppe, Fabbrini, Giovanni, Berardelli, Alfredo, Stocchi, Fabrizio, Barone, Paolo, Picillo, Marina, De Michele, Giuseppe, De Mari, Michele, Dell'Aquila, Claudia, Iliceto, Gianni, Toni, Vincenzo, Trianni, Giorgio, Annesi, Grazia, Saddi, Valeria, Cossu, Gianni, Melis, Maurizio

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Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism von Quadri, Marialuisa, Fang, Mingyan, Picillo, Marina, Olgiati, Simone, Breedveld, Guido J., Graafland, Josja, Wu, Bin, Xu, Fengping, Erro, Roberto, Amboni, Marianna, Pappatà, Sabina, Quarantelli, Mario, Annesi, Grazia, Quattrone, Aldo, Chien, Hsin F., Barbosa, Egberto R., Oostra, Ben A., Barone, Paolo, Wang, Jun, Bonifati, Vincenzo

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Epidemiology and a novel procedure for large scale analysis of CFTR rearrangements in classic and atypical CF patients: A multicentric Italian study von Tomaiuolo, R, Sangiuolo, F, Bombieri, C, Bonizzato, A, Cardillo, G, Raia, V, D'Apice, M.R, Bettin, M.D, Pignatti, P.F, Castaldo, G, Novelli, G

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DNA methylation patterns identify subgroups of pancreatic neuroendocrine tumors with clinical association von Lakis, Vanessa, Lawlor, Rita T., Newell, Felicity, Patch, Ann-Marie, Mafficini, Andrea, Sadanandam, Anguraj, Koufariotis, Lambros T., Johnston, Rebecca L., Leonard, Conrad, Wood, Scott, Rusev, Borislav, Corbo, Vincenzo, Luchini, Claudio, Cingarlini, Sara, Landoni, Luca, Salvia, Roberto, Milella, Michele, Chang, David, Bailey, Peter, Jamieson, Nigel B., Duthie, Fraser, Gingras, Marie-Claude, Muzny, Donna M., Wheeler, David A., Gibbs, Richard A., Milione, Massimo, Pederzoli, Paolo, Samra, Jaswinder S., Gill, Anthony J., Johns, Amber L., Pearson, John V., Biankin, Andrew V., Grimmond, Sean M., Waddell, Nicola, Nones, Katia, Scarpa, Aldo

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Author Correction: Pan-cancer analysis of whole genomes von Aaltonen, Lauri A., Abascal, Federico, Abeshouse, Adam, Aburatani, Hiroyuki, Adams, David J., Agrawal, Nishant, Ahn, Keun Soo, Ahn, Sung-Min, Aikata, Hiroshi, Akbani, Rehan, Akdemir, Kadir C., Al-Ahmadie, Hikmat, Al-Sedairy, Sultan T., Al-Shahrour, Fatima, Alawi, Malik, Albert, Monique, Aldape, Kenneth, Alexandrov, Ludmil B., Ally, Adrian, Alsop, Kathryn, Alvarez, Eva G., Amary, Fernanda, Amin, Samirkumar B., Aminou, Brice, Ammerpohl, Ole, Anderson, Matthew J., Ang, Yeng, Antonello, Davide, Anur, Pavana, Aparicio, Samuel, Appelbaum, Elizabeth L., Arai, Yasuhito, Aretz, Axel, Arihiro, Koji, Ariizumi, Shun-ichi, Armenia, Joshua, Arnould, Laurent, Asa, Sylvia, Assenov, Yassen, Atwal, Gurnit, Aukema, Sietse, Auman, J. Todd, Aure, Miriam R. R., Awadalla, Philip, Aymerich, Marta, Bader, Gary D., Baez-Ortega, Adrian, Bailey, Matthew H., Bailey, Peter J., Balasundaram, Miruna, Balu, Saianand, Bandopadhayay, Pratiti, Banks, Rosamonde E., Barbi, Stefano, Barbour, Andrew P., Barenboim, Jonathan, Barnholtz-Sloan, Jill, Barr, Hugh, Barrera, Elisabet, Bartlett, John, Bartolome, Javier, Bassi, Claudio, Bathe, Oliver F., Baumhoer, Daniel, Bavi, Prashant, Baylin, Stephen B., Bazant, Wojciech, Beardsmore, Duncan, Beck, Timothy A., Behjati, Sam, Behren, Andreas, Niu, Beifang, Bell, Cindy, Beltran, Sergi, Benz, Christopher, Berchuck, Andrew, Bergmann, Anke K., Bergstrom, Erik N., Berman, Benjamin P., Berney, Daniel M., Bernhart, Stephan H., Beroukhim, Rameen, Berrios, Mario, Bersani, Samantha, Bertl, Johanna, Betancourt, Miguel, Bhandari, Vinayak, Bhosle, Shriram G., Biankin, Andrew V., Bieg, Matthias, Bigner, Darell, Binder, Hans, Birney, Ewan, Birrer, Michael, Biswas, Nidhan K., Bjerkehagen, Bodil, Bodenheimer, Tom, Boice, Lori, Bonizzato, Giada, De Bono, Johann S.

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Author Correction: Comprehensive molecular characterization of mitochondrial genomes in human cancers von Yuan, Yuan, Ju, Young Seok, Kim, Youngwook, Li, Jun, Wang, Yumeng, Yoon, Christopher J., Yang, Yang, Martincorena, Inigo, Creighton, Chad J., Weinstein, John N., Xu, Yanxun, Han, Leng, Kim, Hyung-Lae, Nakagawa, Hidewaki, Park, Keunchil, Campbell, Peter J., Liang, Han

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Author Correction: Divergent mutational processes distinguish hypoxic and normoxic tumours von Bhandari, Vinayak, Li, Constance H., Bristow, Robert G., Boutros, Paul C.

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PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology von Wong, Tsz Hang, Chiu, Wang Zheng, Breedveld, Guido J., Li, Ka Wan, Verkerk, Annemieke J. M. H., Hondius, David, Hukema, Renate K., Seelaar, Harro, Frick, Petra, Severijnen, Lies-Anne, Lammers, Gert-Jan, Lebbink, Joyce H. G., van Duinen, Sjoerd G., Kamphorst, Wouter, Rozemuller, Annemieke J., Bakker, E. Bert, Neumann, Manuela, Willemsen, Rob, Bonifati, Vincenzo, Smit, August B., van Swieten, John

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DNAJC6 Mutations Associated With Early-Onset Parkinson's Disease von Olgiati, Simone, Quadri, Marialuisa, Fang, Mingyan, Rood, Janneke P.M.A., Saute, Jonas A., Chien, Hsin Fen, Bouwkamp, Christian G., Graafland, Josja, Minneboo, Michelle, Breedveld, Guido J., Zhang, Jianguo, Verheijen, Frans W., Boon, Agnita J.W., Kievit, Anneke J.A., Jardim, Laura Bannach, Mandemakers, Wim, Barbosa, Egberto Reis, Rieder, Carlos R.M., Leenders, Klaus L., Wang, Jun, Bonifati, Vincenzo

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Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis von Castellani, Carlo, Gomez Lira, Macarena, Frulloni, Luca, Delmarco, Antonella, Marzari, Maria, Bonizzato, Alberto, Cavallini, Giorgio, Pignatti, PierFranco, Mastella, Gianni

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372 Challenging diagnosis when CF or CFTR-related disorders are suspected: from genotype to phenotype and theratype von Melotti, P., Gerotto, M., Kleinfelder, K., Sorio, C., Terlizzi, V., Krivec, U., Pascolo, P., Tomba, F., Massella, A., Pintani, E., Veronesi, G., Hristodor, A., Bertini, M., Cipolli, M., Bonizzato, A., Savoia, A.

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PINK1 heterozygous rare variants: prevalence, significance and phenotypic spectrum von Marongiu, Roberta, Ferraris, Alessandro, Ialongo, Tàmara, Michiorri, Silvia, Soleti, Francesco, Ferrari, Francesca, Elia, Antonio E, Ghezzi, Daniele, Albanese, Alberto, Altavista, Maria Concetta, Antonini, Angelo, Barone, Paolo, Brusa, Livia, Cortelli, Pietro, Martinelli, Paolo, Pellecchia, Maria Teresa, Pezzoli, Gianni, Scaglione, Cesa, Stanzione, Paolo, Tinazzi, Michele, Zecchinelli, Anna, Zeviani, Massimo, Cassetta, Emanuele, Garavaglia, Barbara, Dallapiccola, Bruno, Bentivoglio, Anna Rita, Valente, Enza Maria

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Highly preferential association of NonF508del CF mutations with the M470 allele von Ciminelli, B.M, Bonizzato, A, Bombieri, C, Pompei, F, Gabaldo, M, Ciccacci, C, Begnini, A, Holubova, A, Zorzi, P, Piskackova, T, Macek, M, Castellani, C, Modiano, G, Pignatti, P.F

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