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