Ausgabe 3/2007
Inhalt (11 Artikel)
Bioinformatic analysis of human CNS-expressed ion channels as candidates for episodic nervous system disorders
Jan Freudenberg, Ying-Hui Fu, Louis J. Ptáček
Evaluation of autism traits in Angelman syndrome: a resource to unfold autism genes
Maria Teresa Bonati, Silvia Russo, Palma Finelli, Maria Rosa Valsecchi, Francesca Cogliati, Florinda Cavalleri, Wendy Roberts, Maurizio Elia, Lidia Larizza
Association study of cholesterol-related genes in Alzheimer’s disease
M. Axel Wollmer, Kristel Sleegers, Martin Ingelsson, Cezary Zekanowski, Nathalie Brouwers, Aleksandra Maruszak, Fabienne Brunner, Kim-Dung Huynh, Lena Kilander, Rose-Marie Brundin, Marie Hedlund, Vilmantas Giedraitis, Anna Glaser, Sebastiaan Engelborghs, Peter P. De Deyn, Elisabeth Kapaki, Magdalini Tsolaki, Makrina Daniilidou, Dimitra Molyva, George P. Paraskevas, Dietmar R. Thal, Maria Barcikowska, Jacek Kuznicki, Lars Lannfelt, Christine Van Broeckhoven, Roger M. Nitsch, Christoph Hock, Andreas Papassotiropoulos
The cholesteryl ester transfer protein (CETP) gene and the risk of Alzheimer’s disease
Alejandro Arias-Vásquez, Aaron Isaacs, Yurii S. Aulchenko, Albert Hofman, Ben A. Oostra, Monique Breteler, Cornelia M. van Duijn
Association of progesterone receptor with migraine-associated vertigo
Hane Lee, Lauren Sininger, Joanna C. Jen, Yoon-Hee Cha, Robert W. Baloh, Stanley F. Nelson
Influence of CCR5-Δ32 genotype in Spanish population with multiple sclerosis
D. Otaegui, J. Ruíz-Martínez, J. Olaskoaga, J. I. Emparanza, A. López de Munain
Identification of the porcine homologous of human disease causing trinucleotide repeat sequences
Lone Bruhn Madsen, Bo Thomsen, Christina Ane Elisabeth Sølvsten, Christian Bendixen, Merete Fredholm, Arne Lund Jørgensen, Anders Lade Nielsen
Confirmation of region-specific patterns of gene expression in the human brain
Carl Ernst, Adolfo Sequeira, Tim Klempan, Neil Ernst, Jarlath ffrench-Mullen, Gustavo Turecki
A large deletion and novel point mutations in the calpain 3 gene (CAPN3) in Bulgarian LGMD2A patients
Albena Todorova, Bilyana Georgieva, Ivailo Tournev, Tihomir Todorov, Nadja Bogdanova, Vanyo Mitev, Clemens R. Mueller, Ivo Kremensky, Jürgen Horst
A de novo SPAST mutation leading to somatic mosaicism is associated with a later age at onset in HSP
Christel Depienne, Estelle Fedirko, Jean-Marc Faucheux, Sylvie Forlani, Bernard Bricka, Cyril Goizet, Sylvie Lesourd, Giovanni Stevanin, Merle Ruberg, Alexandra Durr, Alexis Brice
Age at onset in sod1-mediated amyotrophic lateral sclerosis shows familiality
Isabella Fogh, Fruhling Rijsdijk, Peter M. Andersen, Pak C. Sham, Joanne Knight, Benjamin Neale, Diane McKenna-Yasek, Vincenzo Silani, Robert H. Brown Jr., John F. Powell, Ammar Al-Chalabi