Mutations of optineurin in amyotrophic lateral sclerosis

Hirofumi Maruyama, Hiroyuki Morino, Hidefumi Ito, +24

Nature

Amyotrophic Lateral SclerosisNeurological DisorderNeurologyNeuroscienceNeuropathology +2

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

S Nagafuchi, Hiroko Yanagisawa, Keiko Sato, +20

Nature Genetics

Natural SciencesGeneticsPallidoluysian Atrophy ExpansionChromosome 12PMolecular Biology +5

Brain-derived growth factor and nerve growth factor concentrations are decreased in the substantia nigra in Parkinson's disease

Makio Mogi, Akifumi Togari, Tomoyoshi Kondo, +5

Neuroscience Letters

Substantia NigraNeurophysiologyParkinson DiseasePhysiologySocial Sciences +7

Caspase activities and tumor necrosis factor receptor R1 (p55) level are elevated in the substantia nigra from Parkinsonian brain

Makio Mogi, Akifumi Togari, Toshikazu Kondo, +5

Journal of Neural Transmission

Substantia NigraMedicineCell DeathNeuropharmacologyNeurochemical Biomarkers +10

DNA analysis in hereditary dentatorubral-pallidoluysian atrophy

Osamu Komure, Akira Sano, Naoki Nishino, +7

Neurology

A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration

M. Yasuda, Toshio Kawamata, Osamu Komure, +11

Neurology

SCA8 Repeat Expansion: Large CTA/CTG Repeat Alleles Are More Common in Ataxic Patients, Including Those with SCA6

Yuishin Izumi, Hirofumi Maruyama, Masaya Oda, +9

The American Journal of Human Genetics

Allelic VariantGenetic DisorderGeneticsGenetic EpidemiologyPathology +4

Somatic mosaicism of CAG repeat in dentatorubral-pallidoluysian atrophy (DRPLA)

Shuichi Ueno, Keiji Kondoh, Yasunori Komure, +5

Human Molecular Genetics

Triggering of neuronal cell death by accumulation of activated SEK1 on nuclear polyglutamine aggregations in PML bodies

Shingo Yasuda, Kiyoshi Inoue, Miho Hirabayashi, +12

Genes to Cells

Contribution of the interleukin‐1β gene polymorphism in multiple system atrophy

Masataka Nishimura, Hideshi Kawakami, Osamu Komure, +6

Movement Disorders