AAAAAA

   
Results: 1-10 |
Results: 10
Genetic analysis of synphilin-1 in familial Parkinson's disease
Authors: Farrer, M Destee, A Levecque, C Singleton, A Engelender, S Becquet, E Mouroux, V Richard, F Defebvre, L Crook, R Hernandez, D Ross, CA Hardy, J Amouyel, P Chartier-Harlin, MC
Citation: M. Farrer et al., Genetic analysis of synphilin-1 in familial Parkinson's disease, NEUROBIOL D, 8(2), 2001, pp. 317-323
Inducible expression of mutant alpha-synuclein decreases proteasome activity and increases sensitivity to mitochondria-dependent apoptosis
Authors: Tanaka, Y Engelender, S Igarashi, S Rao, RK Wanner, T Tanzi, RE Sawa, A Dawson, VL Dawson, TM Ross, CA
Citation: Y. Tanaka et al., Inducible expression of mutant alpha-synuclein decreases proteasome activity and increases sensitivity to mitochondria-dependent apoptosis, HUM MOL GEN, 10(9), 2001, pp. 919-926
No pathogenic mutations in the synphilin-1 gene in Parkinson's disease
Authors: Bandopadhyay, R de Silva, R Khan, N Graham, E Vaughan, J Engelender, S Ross, C Morris, H Morris, C Wood, NW Daniel, S Lees, A
Citation: R. Bandopadhyay et al., No pathogenic mutations in the synphilin-1 gene in Parkinson's disease, NEUROSCI L, 307(2), 2001, pp. 125-127
A new strategy to decrease N-methyl-D-aspartate (NMDA) receptor coactivation: Inhibition of D-serine synthesis by converting serine racemase into an eliminase
Authors: Panizzutti, R De Miranda, J Ribeiro, C Engelender, S Wolosker, H
Citation: R. Panizzutti et al., A new strategy to decrease N-methyl-D-aspartate (NMDA) receptor coactivation: Inhibition of D-serine synthesis by converting serine racemase into an eliminase, P NAS US, 98(9), 2001, pp. 5294-5299
Organization of the human synphilin-1 gene, a candidate for Parkinson's disease
Authors: Engelender, S Wanner, T Kleiderlein, JJ Wakabayashi, K Tsuji, S Takahashi, H Ashworth, R Margolis, RL Ross, CA
Citation: S. Engelender et al., Organization of the human synphilin-1 gene, a candidate for Parkinson's disease, MAMM GENOME, 11(9), 2000, pp. 763-766
Human serine racemase: moleular cloning, genomic organization and functional analysis
Authors: De Miranda, J Santoro, A Engelender, S Wolosker, H
Citation: J. De Miranda et al., Human serine racemase: moleular cloning, genomic organization and functional analysis, GENE, 256(1-2), 2000, pp. 183-188
Human huntingtin-associated protein (HAP-1) gene: genomic organisation andan intragenic polymorphism
Authors: Nasir, J Lafuente, MJ Duan, K Colomer, V Engelender, S Ingersoll, R Margolis, RL Ross, CA Hayden, MR
Citation: J. Nasir et al., Human huntingtin-associated protein (HAP-1) gene: genomic organisation andan intragenic polymorphism, GENE, 254(1-2), 2000, pp. 181-187
Synphilin-1 is present in Lewy bodies in Parkinson's disease
Authors: Wakabayashi, K Engelender, S Yoshimoto, M Tsuji, S Ross, CA Takahashi, H
Citation: K. Wakabayashi et al., Synphilin-1 is present in Lewy bodies in Parkinson's disease, ANN NEUROL, 47(4), 2000, pp. 521-523
Synphilin-1 associates with alpha-synuclein and promotes the formation of cytosolic inclusions
Authors: Engelender, S Kaminsky, Z Guo, X Sharp, AH Amaravi, RK Kleiderlein, JJ Margolis, RL Troncoso, JC Lanahan, AA Worley, PF Dawson, VL Dawson, TM Ross, CA
Citation: S. Engelender et al., Synphilin-1 associates with alpha-synuclein and promotes the formation of cytosolic inclusions, NAT GENET, 22(1), 1999, pp. 110-114
Chromosomal localization of the Huntingtin associated protein (HAP-1) genein mouse and humans with radiation hybrid and interspecific backcross mapping
Authors: Nasir, J Maclean, A Engelender, S Duan, K Margolis, RL Kleiderlein, JJ Ross, CA Hayden, MR
Citation: J. Nasir et al., Chromosomal localization of the Huntingtin associated protein (HAP-1) genein mouse and humans with radiation hybrid and interspecific backcross mapping, MAMM GENOME, 10(4), 1999, pp. 397-398
Risultati: 1-10 |