Suchergebnisse - Alan Medlar
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1
Wasabi: An Integrated Platform for Evolutionary Sequence Analysis and Data Visualization von Andres Veidenberg, Alan Medlar, Ari Löytynoja
Veröffentlicht 2015Artigo -
2
PANNZER2: a rapid functional annotation web server von Petri Törönen, Alan Medlar, Liisa Holm
Veröffentlicht 2018Artigo -
3
Phospholipase A2 Receptor (PLA2R1) Sequence Variants in Idiopathic Membranous Nephropathy von Marieke J. H. Coenen, Julia M. Hofstra, Hanna Dębiec, Horia Stanescu, Alan Medlar, Bénédicte Stengel, Anne Boland, Johanne M. Groothuismink, Detlef Böckenhauer, S Powis, Peter W. Mathieson, Paul Brenchley, Robert Kleta, Jack F.M. Wetzels, Pierre Ronco
Veröffentlicht 2013Artigo -
4
Mutations in the autoregulatory domain of β‐tubulin 4a cause hereditary dystonia von Joshua Hersheson, Niccolò E. Mencacci, Mary B. Davis, Nicola MacDonald, Daniah Trabzuni, Mina Ryten, Alan Pittman, Reema Paudel, Eleanna Kara, Katherine A. Fawcett, Vincent Plagnol, Kailash P. Bhatia, Alan Medlar, Horia Stanescu, John Hardy, Robert Kleta, Nicholas Wood, Henry Houlden
Veröffentlicht 2012Artigo -
5
Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actin-regulatory gene <i>WDR1 </i> von Ariane Standing, Dessislava Malinova, Ying Hong, Julien Record, Dale Moulding, Michael P. Blundell, Karolin Nowak, Hannah E. Jones, Ebun Omoyinmi, Kimberly Gilmour, Alan Medlar, Horia Stanescu, Robert Kleta, Glenn Anderson, Sira Nanthapisal, Sónia Gomes, Nigel Klein, Despina Eleftheriou, Adrian J. Thrasher, Paul Brogan
Veröffentlicht 2016Artigo -
6
Risk HLA-DQA1 and PLA<sub>2</sub>R1 Alleles in Idiopathic Membranous Nephropathy von H.C. Stanescu, Mauricio Arcos‐Burgos, Alan Medlar, Detlef Böckenhauer, Anna Köttgen, L Dragomirescu, C Voinescu, Nisha Patel, Kathryn E. Pearce, Michael Hubank, Henry A. F. Stephens, V. Laundy, Sandosh Padmanabhan, A. Zawadzka, Julia M. Hofstra, Marieke J. H. Coenen, Martin den Heijer, Lambertus A. Kiemeney, Delphine Bacq‐Daian, Bénédicte Stengel, Stephen H. Powis, Paul Brenchley, J. Feehally, Andrew J. Rees, Hanna Dębiec, J F M Wetzels, Pierre Ronco, Peter W. Mathieson, Robert Kleta
Veröffentlicht 2011Artigo -
7
Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations von Graciana Jaureguiberry, Muriel De La Dure‐Molla, David Parry, Mickaël Quentric, Nina Himmerkus, Toshiyasu Koike, James A. Poulter, Enriko Klootwijk, Steven L. Robinette, Alexander J. Howie, Vaksha Patel, Marie-Lucile Figueres, Horia Stanescu, Naomi Issler, Jeremy K. Nicholson, Detlef Böckenhauer, Christopher Laing, Stephen B. Walsh, David A. McCredie, Sue Povey, Audrey Asselin, Arnaud Picard, Aurore Coulomb, Alan Medlar, Isabelle Bailleul‐Forestier, Alain Verloès, Cédric Le Caignec, G. Roussey, J. Guiol, Bertrand Isidor, Clare V. Logan, Richard F. Shore, Colin A. Johnson, C.F. Inglehearn, Suhaila Al‐Bahlani, Matthieu Schmittbuhl, François Clauss, Mathilde Huckert, Virginie Laugel, Emmanuelle Ginglinger, Sandra Pajarola, Giuseppina Spartà, Deborah Bartholdi, Anita Rauch, Marie-Claude Addor, Paulo Márcio Yamaguti, H.P.N. Safatle, Ana Carolina Acevedo, Hercílio Martelli‐Júnior, Pedro E. dos Santos Netos, Ricardo D. Coletta, Sandra Gruessel, Carolin Sandmann, Denise Ruehmann, Craig B. Langman, Steven J. Scheinman, Didem Özdemır, Thomas C. Hart, P. Suzanne Hart, Ute Neugebauer, Eberhard Schlatter, Pascal Houillier, William A. Gahl, Miikka Vikkula, Agnès Bloch‐Zupan, Markus Bleich, Hiroshi Kitagawa, Robert J. Unwin, Alan J. Mighell, Ariane Berdal, Robert Kleta
Veröffentlicht 2013Artigo -
8
The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screens von Naihui Zhou, Yuxiang Jiang, Timothy Bergquist, Alexandra Lee, Balint Z Kacsoh, Alex W. Crocker, Kimberley A. Lewis, George P. Georghiou, Huy Nguyen, Md-Nafiz Hamid, L. Taylor Davis, Tunca Doğan, Volkan Atalay, Ahmet Süreyya Rifaioğlu, Alperen Dalkıran, Rengül Çetin-Atalay, Chengxin Zhang, Rebecca L. Hurto, Peter L. Freddolino, Yang Zhang, Prajwal Bhat, Fran Supek, José M. Fernández, Branislava Gemović, Vladimir Perović, Radoslav Davidović, Neven Šumonja, Nevena Veljković, Ehsaneddin Asgari, Mohammad R. K. Mofrad, Giuseppe Profiti, Castrense Savojardo, Pier Luigi Martelli, Rita Casadio, Florian Boecker, Heiko Schoof, Indika Kahanda, Natalie Thurlby, Alice C. McHardy, Alexandre Renaux, Rabie Saidi, Julian Gough, Alex A. Freitas, Magdalena Antczak, Fábio Fabris, Mark N. Wass, Jie Hou, Jianlin Cheng, Zheng Wang, Alfonso E. Romero, Alberto Paccanaro, Haixuan Yang, Tatyana Goldberg, Chenguang Zhao, Liisa Holm, Petri Törönen, Alan Medlar, Elaine Zosa, Itamar Borukhov, Ilya B. Novikov, Angela D. Wilkins, Olivier Lichtarge, Po-Han Chi, Wei-Cheng Tseng, Michal Linial, Peter W. Rose, Christophe Dessimoz, Vedrana Vidulin, Sašo Džeroski, Ian Sillitoe, Sayoni Das, Jonathan Lees, David T. Jones, Cen Wan, Domenico Cozzetto, Rui Fa, Mateo Torres, Alex Warwick Vesztrocy, José Manuel Rodrı́guez, Michael L. Tress, Marco Frasca, Marco Notaro, Giuliano Grossi, Alessandro Petrini, Matteo Ré, Giorgio Valentini, Marco Mesiti, Daniel B. Roche, Jonas Reeb, David W. Ritchie, Sabeur Aridhi, Seyed Ziaeddin Alborzi, Marie‐Dominique Devignes, Da Chen Emily Koo, Richard Bonneau, Vladimir Gligorijević, Meet Barot, Hai Fang, Stefano Toppo, Enrico Lavezzo
Veröffentlicht 2019Artigo
Suchwerkzeuge:
Ähnliche Schlagworte
Biology
Gene
Genetics
Computational biology
Kidney
Medicine
Mutation
Allele
Annotation
Computer science
Endocrinology
Function (biology)
Genome
Genomics
Genotype
Glomerulonephritis
Immunology
Internal medicine
Membranous nephropathy
World Wide Web
Actin
Amelogenesis imperfecta
Antigen
Benchmark (surveying)
Biochemistry
Bioinformatics
Cell biology
Clade
Context (archaeology)
DNA sequencing