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Results:
1-11
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Results: 11
Authors:
Hadano, S
Hand, CK
Osuga, H
Yanagisawa, Y
Otomo, A
Devon, RS
Miyamoto, N
Showguchi-Miyata, J
Okada, Y
Singaraja, R
Figlewicz, DA
Kwiatkowski, T
Hosler, BA
Sagie, T
Skaug, J
Nasir, J
Brown, RH
Scherer, SW
Rouleau, GA
Hayden, MR
Ikeda, JE
Citation: S. Hadano et al., A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2 (vol 29, pg 166, 2001), NAT GENET, 29(3), 2001, pp. 352-352
Authors:
Hadano, S
Hand, CK
Osuga, H
Yanagisawa, Y
Otomo, A
Devon, RS
Miyamoto, N
Showguchi-Miyata, J
Okada, Y
Singaraja, R
Figlewicz, DA
Kwiatkowski, T
Hosler, BA
Sagie, T
Skaug, J
Nasir, J
Brown, RH
Scherer, SW
Rouleau, GA
Hayden, MR
Ikeda, JE
Citation: S. Hadano et al., A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2, NAT GENET, 29(2), 2001, pp. 166-173
Authors:
Doroudchi, MM
Minotti, S
Figlewicz, DA
Durham, HD
Citation: Mm. Doroudchi et al., Nitrotyrosination contributes minimally to toxicity of mutant SOD1 associated with ALS, NEUROREPORT, 12(6), 2001, pp. 1239-1243
Cultured glial cells are resistant to the effects of motor neurone disease-associated SOD1 mutations
Authors:
Williams, RE
Cookson, MR
Fray, AE
Manning, PM
Menzies, FM
Figlewicz, DA
Shaw, PJ
Citation: Re. Williams et al., Cultured glial cells are resistant to the effects of motor neurone disease-associated SOD1 mutations, NEUROSCI L, 302(2-3), 2001, pp. 146-150
Authors:
Orrell, RW
Figlewicz, DA
Citation: Rw. Orrell et Da. Figlewicz, Clinical implications of the genetics of ALS and other motor neuron diseases, NEUROLOGY, 57(1), 2001, pp. 9-17
Authors:
Ingram, JL
Stodgell, CJ
Hyman, SL
Figlewicz, DA
Weitkamp, LR
Rodier, PM
Citation: Jl. Ingram et al., Discovery of allelic variants of HOXA1 and HOXB1: Genetic susceptibility to autism spectrum disorders, TERATOLOGY, 62(6), 2000, pp. 393-405
Authors:
Mohajeri, MH
Figlewicz, DA
Bohn, MC
Citation: Mh. Mohajeri et al., Intramuscular grafts of myoblasts genetically modified to secrete glial cell line-derived neurotrophic factor prevent motoneuron loss and disease progression in a mouse model of familial amyotrophic lateral sclerosis, HUM GENE TH, 10(11), 1999, pp. 1853-1866
Authors:
Figlewicz, DA
Bird, TD
Citation: Da. Figlewicz et Td. Bird, "Pure" hereditary spastic paraplegias - The story becomes complicated, NEUROLOGY, 53(1), 1999, pp. 5-7
Authors:
Orrell, RW
Tawil, R
Forrester, J
Kissel, JT
Mendell, JR
Figlewicz, DA
Citation: Rw. Orrell et al., Definitive molecular diagnosis of facioscapulohumeral dystrophy, NEUROLOGY, 52(9), 1999, pp. 1822-1826
Authors:
Mithal, NP
Radunovic, A
Figlewicz, DA
McMillan, TJ
Leigh, PN
Citation: Np. Mithal et al., Cells from individuals with SOD-1 associated familial amyotrophic lateral sclerosis do not have an increased susceptibility to radiation-induced freeradical production or DNA damage, J NEUR SCI, 164(1), 1999, pp. 89-92
Authors:
Bruening, W
Roy, J
Giasson, B
Figlewicz, DA
Mushynski, WE
Durham, HD
Citation: W. Bruening et al., Up-regulation of protein chaperones preserves viability of cells expressing toxic Cu/Zn-superoxide dismutase mutants associated with amyotrophic lateral sclerosis, J NEUROCHEM, 72(2), 1999, pp. 693-699
Risultati:
1-11
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