खोज परिणाम - Isabel Tapia‐Páez
- प्रदर्शित 1 - 9 परिणाम 9
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Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia द्वारा Satu Massinen, Kristiina Tammimies, Isabel Tapia‐Páez, Hans Matsson, Marie-Estelle Hokkanen, Ola Söderberg, Ulf Landegren, Eero Ċastrén, Jan-Ακε Gustafsson, Eckardt Treuter, Juha Kere
प्रकाशित 2009Artigo -
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Further evidence for DYX1C1 as a susceptibility factor for dyslexia द्वारा Faten Dahdouh, Heidi Anthoni, Isabel Tapia‐Páez, Myriam Peyrard‐Janvid, Gerd Schulte‐Körne, Andreas Warnke, Helmut Remschmidt, Andreas Ziegler, Juha Kere, Bertram Müller‐Myhsok, Markus M. Nöthen, Johannes Schumacher, Marco Zucchelli
प्रकाशित 2009Artigo -
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Increased Expression of the Dyslexia Candidate Gene DCDC2 Affects Length and Signaling of Primary Cilia in Neurons द्वारा Satu Massinen, Marie‐Estelle Hokkanen, Hans Matsson, Kristiina Tammimies, Isabel Tapia‐Páez, Vanina Dahlström-Heuser, Juha Kuja‐Panula, Jan Burghoorn, Kristian Jeppsson, Peter Swoboda, Myriam Peyrard‐Janvid, Rune Toftgård, Eero Ċastrén, Juha Kere
प्रकाशित 2011Artigo -
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Physical Exercise–Induced Hypoglycemia Caused by Failed Silencing of Monocarboxylate Transporter 1 in Pancreatic β Cells द्वारा Timo Otonkoski, Hong Jiao, Nina Kaminen‐Ahola, Isabel Tapia‐Páez, Mohammed S. Ullah, Laura E. Parton, Frans Schuit, Roel Quintens, Ilkka Sipilä, Ertan Mayatepek, Thomas Meißner, Andrew P. Halestrap, Guy A. Rutter, Juha Kere
प्रकाशित 2007Artigo -
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DCDC2 Mutations Cause a Renal-Hepatic Ciliopathy by Disrupting Wnt Signaling द्वारा Markus Schueler, Daniela A. Braun, Gayathri Chandrasekar, Heon Yung Gee, Timothy D. Klasson, Jan Halbritter, Andrea Bieder, Jonathan D. Porath, Rannar Airik, Weibin Zhou, Joseph J. LoTurco, Alicia Che, Edgar A. Otto, Detlef Böckenhauer, Neil J. Sebire, Tomáš Honzík, Peter C. Harris, Sarah Koon, Meral Gunay‐Aygun, Sophie Saunier, Klaus Zerres, Nadina Ortiz Bruechle, Joost P.H. Drenth, Laurence Pelletier, Isabel Tapia‐Páez, Richard P. Lifton, Rachel H. Giles, Juha Kere, Friedhelm Hildebrandt
प्रकाशित 2014Artigo -
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High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH द्वारा Carl E.G. Bruder, Carina Hirvelä, Isabel Tapia‐Páez, Ingegerd Fransson, Richard Segraves, Greg Hamilton, Xiao Zhang, D. Gareth Evans, Andrew Wallace, Michael E. Baser, Jessica Zucman‐Rossi, Martin Hergersberg, Eugene Boltshauser, Laura Papi, Guy A. Rouleau, G. Poptodorov, Albena Jordanova, Helge Rask‐Andersen, Lan Kluwe, Victor Mautner, Markku Sainio, Gene Hung, Tiit Mathiesen, Claes Möller, Stefan M. Pulst, Henrik Harder, Arvid Heiberg, Mariko Honda, Michihito Niimura, Sigrid Sahlén, Elisabeth Blennow, Donna G. Albertson, Daniel Pinkel, Jan P. Dumanski
प्रकाशित 2001Artigo -
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The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language द्वारा Heidi Anthoni, Lara E. Sucheston, Barbara Lewis, Isabel Tapia‐Páez, Xiaotang Fan, Marco Zucchelli, Mikko Taipale, Catherine M. Stein, Marie-Estelle Hokkanen, Eero Ċastrén, Bruce F. Pennington, Shelley D. Smith, Richard K. Olson, J. Bruce Tomblin, Gerd Schulte‐Körne, Markus M. Nöthen, Johannes Schumacher, Bertram Müller‐Myhsok, Per Hoffmann, Jeffrey W. Gilger, George W. Hynd, Jaana Nopola‐Hemmi, Paavo H. T. Leppänen, Heikki Lyytinen, Jacqueline Schoumans, Magnus Nordenskjöld, Jason Spencer, Davor Stanić, Wah Chin Boon, Evan R. Simpson, Sari Mäkelä, Jan-Ακε Gustafsson, Myriam Peyrard‐Janvid, Sudha K. Iyengar, Juha Kere
प्रकाशित 2012Artigo
खोज साधन:
संबंधित विषय
Biology
Gene
Genetics
Cell biology
Reading (process)
Cilium
Dyslexia
Law
Political science
Allele
Breast cancer
Cancer
Candidate gene
Ciliogenesis
Gene knockdown
Genotype
Medicine
Molecular biology
Mutation
Phenotype
Pronephros
Signal transduction
Single-nucleotide polymorphism
Wnt signaling pathway
Zebrafish
Aromatase
CDKN2A
Cancer research
Cell culture
Chromosome