Issue 3/2004
Content (12 Articles)
Induction of nerve growth factor mRNA in a rat dorsal root ganglion after application of a tourniquet
Sumiko Abe, Ikubumi Mizusawa, Katsuyuki Kanno, Atsuko Yabashi, Miwako Suto, Mikio Kuraya, Takashi Honda, Kouichi Hiraiwa
Glyceraldehyde-derived advanced glycation end products in Alzheimer’s disease
Hiroshi Choei, Nobuyuki Sasaki, Masayoshi Takeuchi, Taku Yoshida, Wataru Ukai, Sho-ichi Yamagishi, Seiji Kikuchi, Toshikazu Saito
Extracellular protein deposition correlates with glial activation and oxidative stress in Creutzfeldt-Jakob and Alzheimer’s disease
Bart Van Everbroeck, Itte Dobbeleir, Michèle De Waele, Evelyn De Leenheir, Ursula Lübke, Jean-Jacques Martin, Patrick Cras
Oligodendrocytes within astrocytes (“emperipolesis”) in the white matter in Creutzfeldt-Jakob disease
Masayuki Shintaku, Chikao Yutani
Cortical ubiquitin-positive inclusions in frontotemporal dementia without motor neuron disease: a quantitative immunocytochemical study
Enikö Kövari, Gabriel Gold, Panteleimon Giannakopoulos, Constantin Bouras
α-Internexin aggregates are abundant in neuronal intermediate filament inclusion disease (NIFID) but rare in other neurodegenerative diseases
Nigel J. Cairns, Kunihiro Uryu, Eileen H. Bigio, Ian R. A. Mackenzie, Marla Gearing, Charles Duyckaerts, Hideaki Yokoo, Yoichi Nakazato, Evelyn Jaros, Robert H. Perry, Steven E. Arnold, Virginia M.-Y. Lee, John Q. Trojanowski
Expression of tyrosine kinases FAK and Pyk2 in 331 human astrocytomas
A. Gutenberg, W. Brück, M. Buchfelder, H. C. Ludwig
Subcortical angiopathic encephalopathy in a German kindred suggests an autosomal dominant disorder distinct from CADASIL
C. Hagel, C. Groden, R. Niemeyer, D. Stavrou, H. J. Colmant
Marked reduction of focal adhesion kinase, serum response factor and myocyte enhancer factor 2C, but increase in RhoA and myostatin in the hindlimb dy mouse muscles
Kunihiro Sakuma, Ryuta Nakao, Shuichiro Inashima, Miyuki Hirata, Toshikazu Kubo, Masahiro Yasuhara
Actin myopathy with nemaline bodies, intranuclear rods, and a heterozygous mutation in ACTA1 (Asp154Asn)
J. M. Schröder, H. Durling, N. Laing
Rimmed vacuoles in facioscapulohumeral muscular dystrophy: a unique ultrastructural feature
Stephan Neudecker, Michael Krasnianski, Erik Bahn, Stephan Zierz