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Table of contents of journal: *Nature genetics (Print)

Results: 51-75/3077

Authors: Osborne, LR Li, M Pober, B Chitayat, D Bodurtha, J Mandel, A Costa, T Grebe, T Cox, S Tsui, LC Scherer, SW
Citation: Lr. Osborne et al., A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome, NAT GENET, 29(3), 2001, pp. 321-325

Authors: Zhao, XP Alvarado, D Rainier, S Lemons, R Hedera, P Weber, CH Tukel, T Apak, M Heiman-Patterson, T Ming, L Bui, M Fink, JK
Citation: Xp. Zhao et al., Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia, NAT GENET, 29(3), 2001, pp. 326-331

Authors: Zou, YR Sunshine, MJ Taniuchi, I Hatam, F Killeen, N Littman, DR
Citation: Yr. Zou et al., Epigenetic silencing of CD4 in T cells committed to the cytotoxic lineage, NAT GENET, 29(3), 2001, pp. 332-336

Authors: Mandel, H Szargel, R Labay, V Elpeleg, O Saada, A Shalata, A Anbinder, Y Berkowitz, D Hartman, C Barak, M Eriksson, S Cohen, N
Citation: H. Mandel et al., The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA, NAT GENET, 29(3), 2001, pp. 337-341

Authors: Saada, A Shaag, A Mandel, H Nevo, Y Eriksson, S Elpeleg, O
Citation: A. Saada et al., Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy, NAT GENET, 29(3), 2001, pp. 342-344

Authors: Verpy, E Masmoudi, S Zwaenepoel, I Leibovici, M Hutchin, TP Del Castillo, I Nouaille, S Blanchard, S Laine, S Popot, JL Moreno, F Mueller, RF Petit, C
Citation: E. Verpy et al., Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus, NAT GENET, 29(3), 2001, pp. 345-349

Authors: Derynck, R Akhurst, RJ Balmain, A
Citation: R. Derynck et al., TGF-beta signaling in tumor suppression and cancer progression (vol 29, pg117, 2001), NAT GENET, 29(3), 2001, pp. 351-351

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

Authors: Avner, P Bruis, T Poras, I Eley, L Ruiz, P Wiles, MV Sousa-Nunes, R Kettleborough, R Rana, A Morrisette, J Bentley, L Goldsworthy, M Haynes, A Herbert, E Southam, L Lehrach, H Weissenbach, J Manenti, G Rodriguez-Tome, P Beddington, R Dunwoodie, S Cox, RD
Citation: P. Avner et al., A radiation hybrid transcript map of the mouse genome (vol 29, pg 194, 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 (vol 29, pg 166, 2001), NAT GENET, 29(3), 2001, pp. 352-352

Citation: Stem-cell politics, NAT GENET, 29(2), 2001, pp. 101-102

Citation: Declaring financial interests, NAT GENET, 29(2), 2001, pp. 102-102

Authors: Shaw, PJ
Citation: Pj. Shaw, Genetic inroads in familial ALS, NAT GENET, 29(2), 2001, pp. 103-104

Authors: Werner, T
Citation: T. Werner, The promoter connection, NAT GENET, 29(2), 2001, pp. 105-106

Authors: Chamberlin, HM
Citation: Hm. Chamberlin, The adaptable lin-39, NAT GENET, 29(2), 2001, pp. 106-107

Authors: Murray, JC
Citation: Jc. Murray, Time for T, NAT GENET, 29(2), 2001, pp. 107-109

Authors: Goldstein, DB
Citation: Db. Goldstein, Islands of linkage disequilibrium, NAT GENET, 29(2), 2001, pp. 109-111

Authors: Derynck, R Akhurst, RJ Balmain, A
Citation: R. Derynck et al., TGF-beta signaling in tumor suppression and cancer progression, NAT GENET, 29(2), 2001, pp. 117-129

Authors: Faddy, MJ Silber, SJ Gosden, RG
Citation: Mj. Faddy et al., Intra-cytoplasmic sperm injection and infertility, NAT GENET, 29(2), 2001, pp. 131-131

Authors: Cai, WW Chow, CW Damani, S Gregory, SG Marra, M Bradley, A
Citation: Ww. Cai et al., An SSLP marker-anchored BAC framework map of the mouse genome, NAT GENET, 29(2), 2001, pp. 133-134

Authors: Sprecher, E Bergman, R Richard, G Lurie, R Shalev, S Petronius, D Shalata, A Anbinder, Y Leibu, R Perlman, I Cohen, N Szargel, R
Citation: E. Sprecher et al., Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin, NAT GENET, 29(2), 2001, pp. 134-136

Authors: Wu, Y Berends, MJW Sijmons, RH Mensink, RGJ Verlind, E Kooi, KA van der Sluis, T Kempinga, C van der Zee, AGJ Hollema, H Buys, CHCM Kleibeuker, JH Hofstra, RMW
Citation: Y. Wu et al., A role for MLH3 in hereditary nonpolyposis colorectal cancer, NAT GENET, 29(2), 2001, pp. 137-138

Authors: Kurahashi, H Emanuel, BS
Citation: H. Kurahashi et Bs. Emanuel, Unexpected high rate of de novo constitutional t(11;22) translocations in sperm from normal males, NAT GENET, 29(2), 2001, pp. 139-140

Authors: Sozen, MA Suzuki, K Tolarova, MM Bustos, T Iglesias, JEF Spritz, RA
Citation: Ma. Sozen et al., Mutation of PVRL1 is associated with sporadic, non-syndromic cleft lip/palate in northern Venezuela, NAT GENET, 29(2), 2001, pp. 141-142

Authors: MacDonald, TJ Brown, KM LaFleur, B Peterson, K Lawlor, C Chen, YD Packer, RJ Cogen, P Stephan, DA
Citation: Tj. Macdonald et al., Expression profiling of medulloblastoma: PDGFRA and the RAS/MAPK pathway as therapeutic targets for metastatic disease, NAT GENET, 29(2), 2001, pp. 143-152
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