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
Homozygous mutations in ARIX (PHOX2A) result in congenital fibrosis of theextraocular muscles type 2
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