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Results: 1-10 |
Results: 10
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
PTPRC (CD45) is not associated with the development of multiple sclerosis in US patients
Authors: Barcellos, LF Caillier, S Dragone, L Elder, M Vittinghoff, E Bucher, P Lincoln, RR Pericak-Vance, M Haines, JL Weiss, A Hauser, SL Oksenberg, JR
Citation: Lf. Barcellos et al., PTPRC (CD45) is not associated with the development of multiple sclerosis in US patients, NAT GENET, 29(1), 2001, pp. 23-24
A conserved sorting-associated protein is mutant in chorea-acanthocytosis
Authors: Rampoldi, L Dobson-Stone, C Rubio, JP Danek, A Chalmers, RM Wood, NW Verellen, C Ferrer, X Malandrini, A Fabrizi, GM Brown, R Vance, J Pericak-Vance, M Rudolf, G Carre, S Alonso, E Manfredi, M Nemeth, AH Monaco, AP
Citation: L. Rampoldi et al., A conserved sorting-associated protein is mutant in chorea-acanthocytosis, NAT GENET, 28(2), 2001, pp. 119-120
Genes - Here today gone tomorrow: A clinician's guide to genetic linkage and association studies
Authors: Manasco, P Rieser, P Pericak-Vance, M
Citation: P. Manasco et al., Genes - Here today gone tomorrow: A clinician's guide to genetic linkage and association studies, ENDOCRINOLO, 10(5), 2000, pp. 328-334
Genome-wide scan for adult onset primary open angle glaucoma
Authors: Wiggs, JL Allingham, RR Hossain, A Kern, J Auguste, J DelBono, EA Broomer, B Graham, FL Hauser, M Pericak-Vance, M Haines, JL
Citation: Jl. Wiggs et al., Genome-wide scan for adult onset primary open angle glaucoma, HUM MOL GEN, 9(7), 2000, pp. 1109-1117
Linkage of the CCR5 Delta 32 mutation with a functional polymorphism of CD45RA
Authors: Liao, HX Montefiori, DC Patel, DD Lee, DM Scott, WK Pericak-Vance, M Haynes, BF
Citation: Hx. Liao et al., Linkage of the CCR5 Delta 32 mutation with a functional polymorphism of CD45RA, J IMMUNOL, 165(1), 2000, pp. 148-157
North Carolina macular dystrophy (MCDR1) locus: A fine resolution genetic map and haplotype analysis
Authors: Small, KW Udar, N Yelchits, S Klein, R Garcia, C Gallardo, G Puech, B Puech, V Saperstein, D Lim, J Haller, J Flaxel, C Kelsell, R Hunt, D Evans, K Lennon, F Pericak-Vance, M
Citation: Kw. Small et al., North Carolina macular dystrophy (MCDR1) locus: A fine resolution genetic map and haplotype analysis, MOL VIS, 5(38-40), 1999, pp. NIL_1-NIL_5
Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15
Authors: Ben Othmane, K Johnson, E Menold, M Graham, FL Ben Hamida, M Hasegawa, O Rogala, AD Ohnishi, A Pericak-Vance, M Hentati, F Vance, JM
Citation: K. Ben Othmane et al., Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15, GENOMICS, 62(3), 1999, pp. 344-349
Spectrum of disease in familial focal and segmental glomerulosclerosis
Authors: Conlon, PJ Lynn, K Winn, MP Quarles, LD Bembe, ML Pericak-Vance, M Speer, M Howell, DN
Citation: Pj. Conlon et al., Spectrum of disease in familial focal and segmental glomerulosclerosis, KIDNEY INT, 56(5), 1999, pp. 1863-1871
Risultati: 1-10 |