Gene expression analyses reveal molecular relationships among 20 regions of the human CNS Richard B. RothPeter HeveziAlbert Zlotnik Original Article 30 March 2006 Pages: 67 - 80
Analysis of gene expression differences between utrophin/dystrophin-deficient vs mdx skeletal muscles reveals a specific upregulation of slow muscle genes in limb muscles Patrick E. BakerJessica A. KearneyJill A. Rafael-Fortney Original Article 09 March 2006 Pages: 81 - 91
Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum protein Ashraf U. MannanJohann BoehmWolfgang Engel Original Article 07 April 2006 Pages: 93 - 103
Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: novel sequence variants in ASPM gene Asma GulMuhammad Jawad HassanWasim Ahmad Original Article 21 April 2006 Pages: 105 - 110
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: another genetic hit in the Mediterranean Natalia CannelliDenise CassandriniFilippo M. Santorelli Original Article 29 March 2006 Pages: 111 - 117
Identification of Alu elements mediating a partial PMP22 deletion Verena MatejasKathrin HuehneBernd Rautenstrauss Original Article 29 March 2006 Pages: 119 - 126
A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12 Stephan ZüchnerMelanie E. KailAllison E. Ashley-Koch Letter to the Editors 25 March 2006 Pages: 127 - 129
A founder effect and mutational hot spots may contribute to the most frequent mutations in the SPG3A gene Michito NamekawaIsabelle NelsonAlexis Brice Letter to the Editors 13 April 2006 Pages: 131 - 132