Kết quả tìm kiếm - Vincenzo A. Gennarino
- Đang hiển thị 1 - 19 kết quả của 19
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microRNAs and genetic diseases Bằng Nicola Meola, Vincenzo A. Gennarino, Sandro Banfi
Được phát hành 2009Artigo -
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miRNeye: a microRNA expression atlas of the mouse eye Bằng Marianthi Karali, Ivana Peluso, Vincenzo A. Gennarino, Marchesa Bilio, Roberta Verde, Giampiero Lago, Pascal Dollé, Sandro Banfi
Được phát hành 2010Artigo -
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UTRdb and UTRsite (RELEASE 2010): a collection of sequences and regulatory motifs of the untranslated regions of eukaryotic mRNAs Bằng Giorgio Grillo, Antonio Turi, Flavio Licciulli, Flavio Mignone, Sabino Liuni, Sandro Banfi, Vincenzo A. Gennarino, David S. Horner, Giulio Pavesi, Ernesto Picardi, Graziano Pesole
Được phát hành 2009Artigo -
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Identification of microRNA-regulated gene networks by expression analysis of target genes Bằng Vincenzo A. Gennarino, Giovanni D’Angelo, Gopuraja Dharmalingam, Serena Fernandez, Giorgio Russolillo, Remo Sanges, Margherita Mutarelli, Vincenzo Belcastro, Andrea Ballabio, Pasquale Verde, Marco Sardiello, Sandro Banfi
Được phát hành 2012Artigo -
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RBM17 Interacts with U2SURP and CHERP to Regulate Expression and Splicing of RNA-Processing Proteins Bằng Antonia De Maio, Hari Krishna Yalamanchili, Carolyn J. Adamski, Vincenzo A. Gennarino, Zhandong Liu, Jun Qin, Sung Yun Jung, Ronald Richman, Harry T. Orr, Huda Y. Zoghbi
Được phát hành 2018Artigo -
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Pumilio proteins utilize distinct regulatory mechanisms to achieve complementary functions required for pluripotency and embryogenesis Bằng Katherine E. Uyhazi, Yiying Yang, Na Liu, Hongying Qi, Xiao Huang, Winifred Mak, Scott D. Weatherbee, Nicola de Prisco, Vincenzo A. Gennarino, Xiaoling Song, Haifan Lin
Được phát hành 2020Artigo -
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Human-specific regulation of MeCP2 levels in fetal brains by microRNA miR-483-5p Bằng Kihoon Han, Vincenzo A. Gennarino, Yoontae Lee, Kaifang Pang, Kazue Hashimoto‐Torii, Sanaa Choufani, Chandrasekhar S. Raju, Michael C. Oldham, Rosanna Weksberg, Pasko Rakić, Zhandong Liu, Huda Y. Zoghbi
Được phát hành 2013Artigo -
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A Gene Network Regulating Lysosomal Biogenesis and Function Bằng Marco Sardiello, Michela Palmieri, Alberto di Ronza, Diego L. Medina, Marta Valenza, Vincenzo A. Gennarino, Chiara Di Malta, Francesca Donaudy, Valerio Embrione, Roman Polishchuk, Sandro Banfi, Giancarlo Parenti, Elena Cattaneo, Andrea Ballabio
Được phát hành 2009Artigo -
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Pumilio1 Haploinsufficiency Leads to SCA1-like Neurodegeneration by Increasing Wild-Type Ataxin1 Levels Bằng Vincenzo A. Gennarino, Ravi K. Singh, Joshua J. White, Antonia De Maio, Kihoon Han, Ji-Yoen Kim, Paymaan Jafar‐Nejad, Alberto di Ronza, Hyojin Kang, Layal S. Sayegh, Thomas Cooper, Harry T. Orr, Roy V. Sillitoe, Huda Y. Zoghbi
Được phát hành 2015Artigo -
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Loss of Ataxin-1 Potentiates Alzheimer’s Pathogenesis by Elevating Cerebral BACE1 Transcription Bằng Jaehong Suh, Donna Romano, Larissa Nitschke, Scott P. Herrick, Britt A. DiMarzio, Volodymyr Dzhala, Jun-Seok Bae, Mary K. Oram, Yuejiao Zheng, Basavaraj Hooli, Kristina Mullin, Vincenzo A. Gennarino, Wilma Wasco, Jeremy D. Schmahmann, Mark W. Albers, Huda Y. Zoghbi, Rudolph E. Tanzi
Được phát hành 2019Artigo -
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NUDT21-spanning CNVs lead to neuropsychiatric disease and altered MeCP2 abundance via alternative polyadenylation Bằng Vincenzo A. Gennarino, Callison E Alcott, Chun‐An Chen, Arindam Chaudhury, Madelyn A. Gillentine, Jill A. Rosenfeld, Sumit Parikh, James W. Wheless, Elizabeth Roeder, Dafne D. G. Horovitz, Erin K. Roney, Janice Smith, Sau Wai Cheung, Wei Li, Joel R. Neilson, Christian P. Schaaf, Huda Y. Zoghbi
Được phát hành 2015Artigo -
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Correction to: MR Imaging in Ataxias: Consensus Recommendations by the Ataxia Global Initiative Working Group on MRI Biomarkers Bằng Gülin Öz, Sirio Cocozza, Pierre‐Gilles Henry, Christophe Lenglet, Andreas Deistung, Jennifer Faber, Adam J. Schwarz, Dagmar Timmann, Koene R. A. Van Dijk, Ian H. Harding, Astrid D. Adarmes-Gómez, Andreas Thieme, Kathrin Reetz, Marcin Rylski, Thiago Junqueira Ribeiro de Rezende, Vincenzo A. Gennarino, Eva‐Maria Ratai, Caterina Mariotti, Anna Nigri, Lorenzo Nanetti, Martina Minnerop, Sylvia Boesch, Elisabetta Indelicato, Chiara Pinardi, Kirsi M. Kinnunen, Niccolò Fuin, Alexander Gussew, Cherie L. Marvel, James M. Joers
Được phát hành 2023Errata/Corrigenda -
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Alternative polyadenylation alters protein dosage by switching between intronic and 3′UTR sites Bằng Nicola de Prisco, Caitlin Ford, Nathan D. Elrod, Winston Lee, Lauren C. Tang, Kai-Lieh Huang, Lin Ai, Ping Ji, Venkata S. Jonnakuti, Lia Boyle, Maximilian Cabaj, Salvatore Botta, Katrin Õunap, Karit Reinson, Monica H. Wojcik, Jill A. Rosenfeld, Weimin Bi, Kristian Tveten, Trine Prescott, Thorsten Gerstner, Audrey Schroeder, Chin‐To Fong, Jaya K. George‐Abraham, Catherine A. Buchanan, Andrea Hanson-Khan, Jonathan A. Bernstein, Aikaterini A. Nella, Wendy K. Chung, Vicky Brandt, Marko Jovanović, Kimara L. Targoff, Hari Krishna Yalamanchili, Eric J. Wagner, Vincenzo A. Gennarino
Được phát hành 2023Artigo -
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A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures Bằng Vincenzo A. Gennarino, Elizabeth E. Palmer, Laura M. McDonell, Li Wang, Carolyn J. Adamski, Amanda Koire, Lauren See, Chun‐An Chen, Christian P. Schaaf, Jill A. Rosenfeld, Jessica A. Panzer, Ute Moog, Shuang Hao, Ann Bye, Edwin P. Kirk, Paweł Stankiewicz, Amy M. Breman, Arran McBride, Tejaswi Kandula, Holly Dubbs, Rebecca Macintosh, Michael Cardamone, Ying Zhu, Kevin Ying, Kerith‐Rae Dias, Megan T. Cho, Lindsay B. Henderson, Berivan Baskin, Paula Morris, Tao Jiang, Mark J. Cowley, Marcel E. Dinger, Tony Roscioli, Oana Caluseriu, Oksana Suchowersky, Rani Sachdev, Olivier Lichtarge, Jianrong Tang, Kym M. Boycott, J. Lloyd Holder, Huda Y. Zoghbi
Được phát hành 2018Artigo -
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Consensus Recommendations for Clinical Outcome Assessments and Registry Development in Ataxias: Ataxia Global Initiative (AGI) Working Group Expert Guidance Bằng Thomas Klockgether, Matthis Synofzik, Saud Alhusaini, Mathieu Anheim, Irina Antonijevic, Tee Ashizawa, Luís Bataller, Mélanie Berard, Enrico Bertini, Sylvia Boesch, Pedro Braga‐Neto, Emanuel Cassou, Edwin H.W. Chan, Rosalind Chuang, Abbie Collins, Joana Damásio, Karina Carvalho Donis, Antoine Duquette, João Durães, Alexandra Dürr, Rebecca Evans, Jennifer Faber, Jennifer Farmer, Vincenzo A. Gennarino, Holm Graeßner, Marcus Grobe‐Einsler, Hasmet Hanagasie, Morteza Heidari, Henry Houlden, Elisabetta Indelicato, Kinya Ishikawa, Heike Jacobi, Laura Bannach Jardim, Yaz Y. Kisanuki, Svetlana Kopishinskaia, Gilbert L ́Italien, Roderick P.P.W.M. Maas, Michelangelo Mancuso, Caterina Mariotti, Norlinah Mohamed Ibrahim, Wolfgang Nachbauer, Andrea H. Németh, Yi Shiau Ng, Katja Obieglo, Osamu Onodera, Puneet Opal, Luís Pereira de Almeida, Susan Perlman, Guido Primiano, M. Renaud, Liana S. Rosenthal, Francesco Saccà, Zahid Sattar, Tanja Schmitz‐Hübsch, Lüdger Schöls, Rebecca Schüle, Lauren Seeberger, Gabriella Silvestri, Anna Sobańska, Bin‐Weng Soong, Achal Kumar Srivastava, Colleen Stoyas, Sophie Tézenas du Montcel, Andreas Thieme, Dagmar Timmann, Adina Tocoian, Andreas Traschütz, Bart van de Warrenburg, Wolfram Ziegler
Được phát hành 2023Revisão -
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CERT1 mutations perturb human development by disrupting sphingolipid homeostasis Bằng Charlotte Gehin, Museer A. Lone, Winston Lee, Laura Capolupo, Sylvia Ho, Adekemi M. Adeyemi, Erica H. Gerkes, Alexander P.A. Stegmann, Estrella López‐Martín, Eva Bermejo, Beatriz Martı́nez-Delgado, Christiane Zweier, Cornelia Kraus, Bernt Popp, Vincent Strehlow, Daniel Gräfe, Ina Knerr, Eppie R. Jones, Stefano Zamuner, Luciano A. Abriata, Vidya Kunnathully, Brandon E Moeller, Anthony Vocat, Samuel Rommelaere, Jean-Philippe Bocquete, Evelyne Ruchti, Greta Limoni, Marine Van Campenhoudt, Samuel Bourgeat, Petra Henklein, Christian Gilissen, Bregje W.M. van Bon, Rolph Pfundt, Marjolein H. Willemsen, Jolanda Schieving, Emanuela Leonardi, Fiorenza Soli, Alessandra Murgia, Hui Guo, Qiumeng Zhang, Kun Xia, Christina Fagerberg, Christoph P. Beier, Martin J. Larsen, Irene Valenzuela, Paula Fernández‐Álvarez, Shiyi Xiong, Robert Śmigiel, Vanesa López‐González, Lluı́s Armengol, Manuela Morleo, Angelo Selicorni, Annalaura Torella, Moira Blyth, Nicola Cooper, Valerie Wilson, Renske Oegema, Yvan Herenger, Aurore Garde, Ange‐Line Bruel, Frédéric Tran Mau‐Them, Alexis B.R. Maddocks, Jennifer Bain, Musadiq A. Bhat, Gregory Costain, Pekka Kannus, Ashish Marwaha, Neena L. Champaigne, Michael J. Friez, Ellen B. Richardson, Vykuntaraju K. Gowda, Varunvenkat M. Srinivasan, Yask Gupta, Tze Y. Lim, Simone Sanna‐Cherchi, Bruno Lemaître, Toshiyuki Yamaji, Kentaro Hanada, John E. Burke, Ana Marija Jakšić, Brian D. McCabe, Paolo De Los Rios, Thorsten Hornemann, Giovanni D’Angelo, Vincenzo A. Gennarino
Được phát hành 2023Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Gene
Genetics
Cell biology
Computational biology
Messenger RNA
Phenotype
Neuroscience
microRNA
Ataxia
Gene expression
Medicine
Untranslated region
Internal medicine
Three prime untranslated region
Disease
Function (biology)
Neurodegeneration
Regulation of gene expression
Alternative splicing
Computer science
DNA microarray
Epigenetics
Gene expression profiling
Gene knockdown
Haploinsufficiency
Hippocampal formation
Intron
MECP2
Medical physics