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Results: 1-8 |
Results: 8
The gene encoding alsin, a protein with three guanine-nucleoticle exchangefactor domains, is mutated in a form of recessive amyotrophic lateral sclerosis (vol 29, pg 160, 2001)
Authors: Yang, Y Hentati, A Deng, HX Dabbagh, O Sasaki, T Hirano, M Hung, WY Ouahchi, K Yan, J Azim, AC Cole, N Gascon, G Yagmour, A Ben-Hamida, M Pericak-Vance, M Hentati, F Siddique, T
Citation: Y. Yang et al., The gene encoding alsin, a protein with three guanine-nucleoticle exchangefactor domains, is mutated in a form of recessive amyotrophic lateral sclerosis (vol 29, pg 160, 2001), NAT GENET, 29(3), 2001, pp. 352-352
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis
Authors: Yang, Y Hentati, A Deng, HX Dabbagh, O Sasaki, T Hirano, M Hung, WY Ouahchi, K Yan, JH Azim, AC Cole, N Gascon, G Yagmour, A Ben-Hamida, M Pericak-Vance, M Hentati, F Siddique, T
Citation: Y. Yang et al., The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis, NAT GENET, 29(2), 2001, pp. 160-165
Markovian timed Petri nets for performance analysis of semiconductor manufacturing systems
Authors: Jeng, MD Xie, XL Hung, WY
Citation: Md. Jeng et al., Markovian timed Petri nets for performance analysis of semiconductor manufacturing systems, IEEE SYST B, 30(5), 2000, pp. 757-771
Influence of Mn-O bond length on carrier localization in La1-x(Ca,Sr)(x)MnO3, where x=0.28 to 0.375
Authors: MacManus-Driscoll, JL Tan, GT Hung, WY Berenov, AV Alonso, JA Blamire, MG Evetts, JE Damay, F Cohen, LF
Citation: Jl. Macmanus-driscoll et al., Influence of Mn-O bond length on carrier localization in La1-x(Ca,Sr)(x)MnO3, where x=0.28 to 0.375, J MATER RES, 15(5), 2000, pp. 1167-1175
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22
Authors: Hosler, BA Siddique, T Sapp, PC Sailor, W Huang, MC Hossain, A Daube, JR Nance, M Fan, CH Kaplan, J Hung, WY McKenna-Yasek, D Haines, JL Pericak-Vance, MA Horvitz, HR Brown, RH
Citation: Ba. Hosler et al., Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22, J AM MED A, 284(13), 2000, pp. 1664-1669
Novel mutations in spastin gene and absence of correlation with age at onset of symptoms
Authors: Hentati, A Deng, HX Zhai, H Chen, W Yang, Y Hung, WY Azim, AC Bohlega, S Tandan, R Warner, C Laing, NG Cambi, F Mitsumoto, H Roos, RP Boustany, RM Ben Hamida, M Hentati, F Siddique, T
Citation: A. Hentati et al., Novel mutations in spastin gene and absence of correlation with age at onset of symptoms, NEUROLOGY, 55(9), 2000, pp. 1388-1390
Increased reactive oxygen species in familial amyotrophic lateral sclerosis with mutations in SOD1
Authors: Ahmed, MS Hung, WY Zu, JS Hockberger, P Siddique, T
Citation: Ms. Ahmed et al., Increased reactive oxygen species in familial amyotrophic lateral sclerosis with mutations in SOD1, J NEUR SCI, 176(2), 2000, pp. 88-94
Multiple transcripts of the human Cu,Zn superoxide dismutase gene
Authors: Hirano, M Hung, WY Cole, N Azim, AC Deng, HX Siddique, T
Citation: M. Hirano et al., Multiple transcripts of the human Cu,Zn superoxide dismutase gene, BIOC BIOP R, 276(1), 2000, pp. 52-56
Risultati: 1-8 |