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

Results: 26-50/3077

Authors: Berger, J Suzuki, T Senti, KA Stubbs, J Schaffner, G Dickson, BJ
Citation: J. Berger et al., Genetic mapping with SNP markers in Drosophila, NAT GENET, 29(4), 2001, pp. 475-481

Authors: Ge, H Liu, ZH Church, GM Vidal, M
Citation: H. Ge et al., Correlation between transcriptome and interactome mapping data from Saccharomyces cerevisiae, NAT GENET, 29(4), 2001, pp. 482-486

Authors: Hughes, JF Coffin, JM
Citation: Jf. Hughes et Jm. Coffin, Evidence for genomic rearrangements mediated by human endogenous retroviruses during primate evolution, NAT GENET, 29(4), 2001, pp. 487-489

Authors: Hodgson, G Hager, JH Volik, S Hariono, S Wernick, M Moore, D Nowak, N Albertson, DG Pinkel, D Collins, C Hanahan, D Gray, JW
Citation: G. Hodgson et al., Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas (vol 29, pg 459, 2001), NAT GENET, 29(4), 2001, pp. 491-491

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 (vol 29, pg 337, 2001), NAT GENET, 29(4), 2001, pp. 491-491

Authors: Tartaglia, M Mehler, EL Goldberg, R Zampino, G Brunner, HG Kremer, H van der Burgt, I Crosby, AH Ion, A Jeffery, S Kalidas, K Patton, MA Kucherlapati, RS Gelb, B
Citation: M. Tartaglia et al., Mutations in the protein tyrosine kinase gene, PTPN11, cause Noonan Syndrome (vol 29, pg 465, 2001), NAT GENET, 29(4), 2001, pp. 491-491

Citation: Genes, drugs and race, NAT GENET, 29(3), 2001, pp. 239-240

Authors: Kastner, DL O'Shea, JJ
Citation: Dl. Kastner et Jj. O'Shea, A fever gene comes in from the cold, NAT GENET, 29(3), 2001, pp. 241-242

Authors: Yen, P
Citation: P. Yen, The fragility of fertility, NAT GENET, 29(3), 2001, pp. 243-244

Authors: Vieland, VJ
Citation: Vj. Vieland, The replication requirement, NAT GENET, 29(3), 2001, pp. 244-245

Authors: Donovan, PJ
Citation: Pj. Donovan, High Oct-ane fuel powers the stem cell, NAT GENET, 29(3), 2001, pp. 246-247

Authors: McLeod, HL
Citation: Hl. Mcleod, Pharmacogenetics: more than skin deep, NAT GENET, 29(3), 2001, pp. 247-248

Authors: Fraser, CM Dando, MR
Citation: Cm. Fraser et Mr. Dando, Genomics and future biological weapons: The need for preventive action by the biomedical community, NAT GENET, 29(3), 2001, pp. 253-256

Authors: Awatramani, R Soriano, P Mai, JJ Dymecki, S
Citation: R. Awatramani et al., An Flp indicator mouse expressing alkaline phosphatase from the ROSA26 locus, NAT GENET, 29(3), 2001, pp. 257-259

Authors: Rovio, AT Marchington, DR Donat, S Schuppe, HC Abe, J Fritsche, E Elliott, DJ Laippala, P Ahola, AL McNay, D Harrison, RF Hughes, B Barrett, T Bailey, DMD Mehmet, D Jequier, AM Hargreave, TB Kao, SH Cummins, JM Barton, DE Cooke, HJ Wei, YH Wichmann, L Poulton, J Jacobs, HT
Citation: At. Rovio et al., Mutations at the mitochondrial DNA polymerase (POLG) locus associated withmale infertility, NAT GENET, 29(3), 2001, pp. 261-262

Authors: Snijders, AM Nowak, N Segraves, R Blackwood, S Brown, N Conroy, J Hamilton, G Hindle, AK Huey, B Kimura, K Law, S Myambo, K Palmer, J Ylstra, B Yue, JP Gray, JW Jain, AN Pinkel, D Albertson, DG
Citation: Am. Snijders et al., Assembly of microarrays for genome-wide measurement of DNA copy number., NAT GENET, 29(3), 2001, pp. 263-264

Authors: Wilson, JF Weale, ME Smith, AC Gratrix, F Fletcher, B Thomas, MG Bradman, N Goldstein, DB
Citation: Jf. Wilson et al., Population genetic structure of variable drug response, NAT GENET, 29(3), 2001, pp. 265-269

Authors: Dyer, RB McMurray, CT
Citation: Rb. Dyer et Ct. Mcmurray, Mutant protein in Huntington disease is resistant to proteolysis in affected brain, NAT GENET, 29(3), 2001, pp. 270-278

Authors: Kawaguchi, TK Skaletsky, H Brown, LG Minx, PJ Cordum, HS Waterston, RH Wilson, RK Silber, S Oates, R Rozen, S Page, DC
Citation: Tk. Kawaguchi et al., The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men, NAT GENET, 29(3), 2001, pp. 279-286

Authors: Trockenbacher, A Suckow, V Foerster, J Winter, J Krauss, S Ropers, HH Schneider, R Schweiger, S
Citation: A. Trockenbacher et al., MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation, NAT GENET, 29(3), 2001, pp. 287-294

Authors: Graeber, TG Eisenberg, D
Citation: Tg. Graeber et D. Eisenberg, Bioinformatic identification of potential autocrine signaling loops in cancers from gene expression profiles, NAT GENET, 29(3), 2001, pp. 295-300

Authors: Hoffman, HM Mueller, JL Broide, DH Wanderer, AA Kolodner, RD
Citation: Hm. Hoffman et al., Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome, NAT GENET, 29(3), 2001, pp. 301-305

Authors: Ioannidis, JPA Ntzani, EE Trikalinos, TA Contopoulos-Ioannidis, DG
Citation: Jpa. Ioannidis et al., Replication validity of genetic association studies, NAT GENET, 29(3), 2001, pp. 306-309

Authors: Birkenhager, R Otto, E Schurmann, MJ Vollmer, M Ruf, EM Maier-Lutz, I Beekmann, F Fekete, A Omran, H Feldmann, D Milford, DV Jeck, N Konrad, M Landau, D Knoers, NVAM Antignac, C Sudbrak, R Kispert, A Hildebrandt, F
Citation: R. Birkenhager et al., Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure, NAT GENET, 29(3), 2001, pp. 310-314

Authors: Nakano, M Yamada, K Fain, J Sener, EC Selleck, CJ Awad, AH Zwaan, J Mullaney, PB Bosley, TM Engle, EC
Citation: M. Nakano et al., Homozygous mutations in ARIX (PHOX2A) result in congenital fibrosis of theextraocular muscles type 2, NAT GENET, 29(3), 2001, pp. 315-320
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