Results: 1-25 | 26-50 | 51-75 | 76-100 | >>

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

Results: 76-100/3077

Authors: Pilpel, Y Sudarsanam, P Church, GM
Citation: Y. Pilpel et al., Identifying regulatory networks by combinatorial analysis of promoter elements, NAT GENET, 29(2), 2001, pp. 153-159

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

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: Walley, AJ Chavanas, S Moffatt, ME Esnouf, RM Ubhi, B Lawrence, R Wong, K Abecasis, GR Jones, EY Harper, JL Hovnanian, A Cookson, WOCM
Citation: Aj. Walley et al., Gene polymorphism in Netherton and common atopic disease, NAT GENET, 29(2), 2001, pp. 175-178

Authors: Braybrook, C Doudney, K Marcano, ACB Arnason, A Bjornsson, A Patton, MA Goodfellow, PJ Moore, GE Stanier, P
Citation: C. Braybrook et al., The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia, NAT GENET, 29(2), 2001, pp. 179-183

Authors: Date, H Onodera, O Tanaka, H Iwabuchi, K Uekawa, K Igarashi, S Koike, R Hiroi, T Yuasa, T Awaya, Y Sakai, T Takahashi, T Nagatomo, H Sekijima, Y Kawachi, I Takiyama, Y Nishizawa, M Fukuhara, N Saito, K Sugano, S Tsuji, S
Citation: H. Date et al., Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is causedby mutations in a new HIT superfamily gene, NAT GENET, 29(2), 2001, pp. 184-188

Authors: Moreira, MC Barbot, C Tachi, N Kozuka, N Uchida, E Gibson, T Mendonca, P Costa, M Barros, J Yanagisawa, T Watanabe, M Ikeda, Y Aoki, M Nagata, T Coutinho, P Sequeiros, J Koenig, M
Citation: Mc. Moreira et al., The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin, NAT GENET, 29(2), 2001, pp. 189-193

Authors: Avner, P Bruls, T Poras, I Eley, L Gas, S Ruiz, P Wiles, MV Sousa-Nunes, R Kettleborough, R Rana, A Morissette, 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, NAT GENET, 29(2), 2001, pp. 194-200

Authors: Hudson, TJ Church, DM Greenaway, S Nguyen, H Cook, A Steen, RG Van Etten, WJ Castle, AB Strivens, MA Trickett, P Heuston, C Davison, C Southwell, A Hardisty, R Varela-Carver, A Haynes, AR Rodriguez-Tome, P Doi, H Ko, MSH Pontius, J Schriml, L Wagner, L Maglott, D Brown, SDM Lander, ES Schuler, G Denny, P
Citation: Tj. Hudson et al., A radiation hybrid map of mouse genes, NAT GENET, 29(2), 2001, pp. 201-205

Authors: Herceg, Z Hulla, W Gell, D Cuenin, C Lleonart, M Jackson, S Wang, ZQ
Citation: Z. Herceg et al., Disruption of Trrap causes early embryonic lethality and defects in cell cycle progression, NAT GENET, 29(2), 2001, pp. 206-211

Authors: Hogema, BM Gupta, M Senephansiri, H Burlingame, TG Taylor, M Jakobs, C Schutgens, RBH Froestl, W Snead, OC Diaz-Arrastia, R Bottiglieri, T Grompe, M Gibson, KM
Citation: Bm. Hogema et al., Pharmacologic rescue of lethal seizures in mice deficient in succinate semialdehyde dehydrogenase, NAT GENET, 29(2), 2001, pp. 212-216

Authors: Jeffreys, AJ Kauppi, L Neumann, R
Citation: Aj. Jeffreys et al., Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex, NAT GENET, 29(2), 2001, pp. 217-222

Authors: Rioux, JD Daly, MJ Silverberg, MS Lindblad, K Steinhart, H Cohen, Z Delmonte, T Kocher, K Miller, K Guschwan, S Kulbokas, EJ O'Leary, S Winchester, E Dewar, K Green, T Stone, V Chow, C Cohen, A Langelier, D Lapointe, G Gaudet, D Faith, J Branco, N Bull, SB McLeod, RS Griffiths, AM Bitton, A Greenberg, GR Lander, ES Siminovitch, KA Hudson, TJ
Citation: Jd. Rioux et al., Genetic variation in the 5q31 cytokine gene cluster confers susceptibilityto Crohn disease, NAT GENET, 29(2), 2001, pp. 223-228

Authors: Daly, MJ Rioux, JD Schaffner, SE Hudson, TJ Lander, ES
Citation: Mj. Daly et al., High-resolution haplotype structure in the human genome, NAT GENET, 29(2), 2001, pp. 229-232

Authors: Johnson, GCL Esposito, L Barratt, BJ Smith, AN Heward, J Di Genova, G Ueda, H Cordell, HJ Eaves, IA Dudbridge, F Twells, RCJ Payne, F Hughes, W Nutland, S Stevens, H Carr, P Tuomilehto-Wolf, E Tuomilehto, J Gough, SCL Clayton, DG Todd, JA
Citation: Gcl. Johnson et al., Haplotype tagging for the identification of common disease genes, NAT GENET, 29(2), 2001, pp. 233-237

Citation: Something old, something new, NAT GENET, 29(1), 2001, pp. 1-2

Authors: Pfeifer, GP
Citation: Gp. Pfeifer, A new verdict for an old convict, NAT GENET, 29(1), 2001, pp. 3-4

Authors: Quackenbush, J
Citation: J. Quackenbush, The power of public access - The human genome project and the scientific process, NAT GENET, 29(1), 2001, pp. 4-6

Authors: Cole, CN
Citation: Cn. Cole, Choreographing mRNA biogenesis, NAT GENET, 29(1), 2001, pp. 6-7

Authors: Saari, JC
Citation: Jc. Saari, The sights along route 65, NAT GENET, 29(1), 2001, pp. 8-9

Authors: Rabino, I
Citation: I. Rabino, How human geneticists in US view commercialization of the Human Genome Project, NAT GENET, 29(1), 2001, pp. 15-16

Authors: Moghadaszadeh, B Petit, N Jaillard, C Brockington, M Roy, SQ Merlini, L Romero, N Estournet, B Desguerre, I Chaigne, D Muntoni, F Topaloglu, H Guicheney, P
Citation: B. Moghadaszadeh et al., Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome, NAT GENET, 29(1), 2001, pp. 17-18

Authors: Miceli-Richard, C Lesage, S Rybojad, M Prieur, AM Manouvrier-Hanu, S Hafner, R Chamaillard, M Zouali, H Thomas, G Hugot, JP
Citation: C. Miceli-richard et al., CARD15 mutations in Blau syndrome, NAT GENET, 29(1), 2001, pp. 19-20

Authors: Oota, H Settheetham-Ishida, W Tiwawech, D Ishida, T Stoneking, M
Citation: H. Oota et al., Human mtDNA and Y-chromosome variation is correlated with matrilocal versus patrilocal residence, NAT GENET, 29(1), 2001, pp. 20-21

Authors: Vorechovsky, I Kralovicova, J Tchilian, E Masterman, T Zhang, ZP Ferry, B Misbah, S Chapel, H Webster, D Hellgren, D Anvret, M Hillert, J Hammarstrom, L Beverley, PC
Citation: I. Vorechovsky et al., Does 77C -> G in PTPRC modify autoimmune disorders linked to the major histocompatibility locus?, NAT GENET, 29(1), 2001, pp. 22-23
Risultati: 1-25 | 26-50 | 51-75 | 76-100 | >>