Neurogenetics

Whole genome expression analyses of single- and double-knock-out mice implicate partially overlapping functions of alpha- and gamma-synuclein
pp. 71-81(11)
Authors: Kuhn, Melanie; Haebig, Karina; Bonin, Michael; Ninkina, Natalia; Buchman, Vladimir; Poths, Sven; Riess, Olaf

The medial and lateral substantia nigra in Parkinson's disease: mRNA profiles associated with higher brain tissue vulnerability
pp. 83-94(12)
Authors: Duke, D.; Moran, L.; Pearce, R.; Graeber, M.

Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson's disease
pp. 95-102(8)
Authors: Taylor, Julie; Hulihan, Mary; Kachergus, Jennifer; Melrose, Heather; Lincoln, Sarah; Hinkle, Kelly; Stone, Jeremy; Ross, Owen; Hauser, Robert; Aasly, Jan; Gasser, Thomas; Payami, Haydeh; Wszolek, Zbigniew; Farrer, Matthew

Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis
pp. 103-109(7)
Authors: Grünewald, Anne; Breedveld, Guido; Lohmann-Hedrich, Katja; Rohé, Christan; König, Inke; Hagenah, Johann; Vanacore, Nicola; Meco, Giuseppe; Antonini, Angelo; Goldwurm, Stefano; Lesage, Suzanne; Dürr, Alexandra; Binkofski, Ferdinand; Siebner, Hartwig; Münchau, Alexander; Brice, Alexis; Oostra, Ben; Klein, Christine; Bonifati, Vincenzo

A novel gene derived from a segmental duplication shows perturbed expression in Alzheimer's disease
pp. 111-120(10)
Authors: Avramopoulos, Dimitrios; Wang, Ruihua; Valle, David; Fallin, M.; Bassett, Susan

Nf1 expression is dependent on strain background: implications for tumor suppressor haploinsufficiency studies
pp. 121-130(10)
Authors: Hawes, Jessica; Tuskan, Robert; Reilly, Karlyne

Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia
pp. 131-135(5)
Authors: Chen, Haijun; Hehn, Christian; Kaczmarek, Leonard; Ment, Laura; Pober, Barbara; Hisama, Fuki

Mutations of the LMNA gene can mimic autosomal dominant proximal spinal muscular atrophy
pp. 137-142(6)
Authors: Rudnik-Schöneborn, Sabine; Botzenhart, Elke; Eggermann, Thomas; Senderek, Jan; Schoser, Benedikt; Schröder, Rolf; Wehnert, Manfred; Wirth, Brunhilde; Zerres, Klaus

Altered neurodevelopment associated with mutations of RSK2: a morphometric MRI study of Coffin-Lowry syndrome
pp. 143-147(5)
Authors: Kesler, Shelli; Simensen, Richard; Voeller, Kytja; Abidi, Fatima; Stevenson, Roger; Schwartz, Charles; Reiss, Allan

Large germline deletions and duplication in isolated cerebral cavernous malformation patients
pp. 149-153(5)
Authors: Felbor, U.; Gaetzner, S.; Verlaan, D.; Vijzelaar, R.; Rouleau, G.; Siegel, A.

NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe
pp. 155-157(3)
Authors: Klebe, Stephan; Lacour, Arnaud; Durr, Alexandra; Stojkovic, Tanya; Depienne, Christel; Forlani, Sylvie; Poea-Guyon, Sandrine; Vuillaume, Isabelle; Sablonniere, Bernard; Vermersch, Patrick; Brice, Alexis; Stevanin, Giovanni