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| Editorial |  Top |
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Symptoms in a 'leaky' mouse pp331 - 332
doi:10.1038/ng0495-331
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(229K)
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| News and Views | Top |
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Pax genes — Paired feet in three camps pp333 - 334
Andrew P. Read
doi:10.1038/ng0495-333
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(335K)
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BRCA1: More than a hereditary breast cancer gene? pp335 - 336
Jeff Boyd
doi:10.1038/ng0495-335
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(216K)
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Progress in prostate cancer pp336 - 338
Lisa Cannon-Albright
& Rosalind Eeles
doi:10.1038/ng0495-336
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(520K)
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| Correspondence | Top |
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Triad-DNA: a model for trinucleotide repeats pp339 - 341
Vitaly V. Kuryavyi
& Thomas M. Jovin
doi:10.1038/ng0495-339
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(468K)
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Towards fully automated genome−wide polymorphism screening pp341 - 342
Kenneth J. Livak, Jeffrey Marmaro
& John A. Todd
doi:10.1038/ng0495-341
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(208K)
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A somatic BRCA1 mutation in an ovarian tumour pp343 - 344
Louise Hosking, John Trowsdale, Hans Nicolai, Ellen Solomon, William Foulkes, Gordon Stamp, Esther Signer
& Alec Jeffreys
doi:10.1038/ng0495-343
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(271K)
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Unique features of the CAG repeats in Machado−Joseph disease pp344 - 345
Hideshi Kawakami, Hirofumi Maruyama, Shigenobu Nakamura, Yoshiya Kawaguchi, Akira Kakizuka, Manabu Doyu
& Gen Sobue
doi:10.1038/ng0495-344
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(178K)
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Anastasia and Anna Anderson p345
R. Richard Schweitzer
doi:10.1038/ng0495-345
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(86K)
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| Progress | Top |
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Positional cloning moves from perditional to traditional pp347 - 350
Francis S. Collins
doi:10.1038/ng0495-347
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(480K)
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| Articles | Top |
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Lung disease in the cystic fibrosis mouse exposed to bacterial pathogens pp351 - 357
Donald J. Davidson, Julia R. Dorin, Gerard McLachlan, Vincent Ranaldi, David Lamb, Catherine Doherty, John Govan
& David J. Porteous
doi:10.1038/ng0495-351
Abstract + references | PDF
(1,052K)
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Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux pp358 - 364
Phaikasame Sanyanusin, Lisa A. Schimmenti, Leslie A. McNoe, Teresa A. Ward, Mary Ella M. Pierpont, Michael J. Sullivan, William B. Dobyns
& Michael R. Eccles
doi:10.1038/ng0495-358
Abstract + references | PDF
(792K)
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Sequence analysis reveals a  −thalassaemia mutation in the DNA of skeletal remains from the archaeological site of Akhziv, Israel pp365 - 368
Dvora Filon, Marina Faerman, Patricia Smith
& Ariella Oppenheim
doi:10.1038/ng0495-365
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(555K)
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Chromosome specific paints from a high resolution flow karyotype of the mouse pp369 - 375
Pamela Rabbitts, Helen Impey, Amanda Heppell-Parton, Cordelia Langford, Charles Tease, Nicholas Lowe, David Bailey, Malcolm Ferguson-Smith
& Nigel Carter
doi:10.1038/ng0495-369
Abstract + references | PDF
(1,054K)
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A site−directed chromosomal translocation induced in embryonic stem cells by Cre-loxP recombination pp376 - 385
Andrew J.H. Smith, Michelle A. De Sousa, Bernard Kwabi-Addo, Amanda Heppell-Parton, Helen Impey
& Pamela Rabbitts
doi:10.1038/ng0495-376
Abstract + references | PDF
(1,281K)
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Domain organization of allele−specific replication within the GABRB3 gene cluster requires a biparental 15q11−13 contribution pp386 - 394
Janine M. LaSalle
& Marc Lalande
doi:10.1038/ng0495-386
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(1,051K)
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Inherited microdeletions in the Angelman and Prader−Willi syndromes define an imprinting centre on human chromosome 15 pp395 - 400
Karin Buiting, Shinji Saitoh, Stephanie Gross, Bärbel Dittrich, Stuart Schwartz, Robert D. Nicholls
& Bernhard Horsthemke
doi:10.1038/ng0495-395
Abstract + references | PDF
(735K)
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In vivo amplification of the androgen receptor gene and progression of human prostate cancer pp401 - 406
Tapio Visakorpi, Eija Hyytinen, Pasi Koivisto, Minna Tanner, Riitta Keinänen, Christian Palmberg, Aarno Palotie, Teuvo Tammela, Jorma Isola
& Olli-P. Kallioniemi
doi:10.1038/ng0495-401
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(715K)
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A paternal−specific methylation imprint marks the alleles of the mouse H19 gene pp407 - 413
Kimberly D. Tremblay, Jennifer R. Saam, Robert S. Ingram, Shirley M. Tilghman
& Marisa S. Bartolomei
doi:10.1038/ng0495-407
Abstract + references | PDF
(805K)
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X−linked thrombocytopenia and Wiskott−Aldrich syndrome are allelic diseases with mutations in the WASP gene pp414 - 417
Anna Villa, Luigi Notarangelo, Paolo Macchi, Elide Mantuano, Giovanni Cavagni, Duilio Brugnoni, Dario Strina, M Cristina Patrosso, Ugo Ramenghi, Maria Grazia Sacco, Alberto Ugazio
& Paolo Vezzoni
doi:10.1038/ng0495-414
Abstract + references | PDF
(401K)
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A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q pp418 - 423
Martine Vaxillaire, Valérie Boccio, Anne Philippi, Corinne Vigouroux, Joe Terwilliger, Philippe Passa, Jacques S. Beckmann, Gilberto Velho, G. Mark Lathrop
& Philippe Froguel
doi:10.1038/ng0495-418
Abstract + references | PDF
(453K)
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The apolipoprotein(a) gene is regulated by sex hormones and acute−phase inducers in YAC transgenic mice pp424 - 431
Kelly A. Frazer, Goutham Narla, Jun Li Zhang
& Edward M. Rubin
doi:10.1038/ng0495-424
Abstract + references | PDF
(899K)
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Optical mapping of lambda bacteriophage clones using restriction endonucleases pp432 - 438
Xun Meng, Kathrine Benson, Kiran Chada, Edward J. Huff
& David C. Schwartz
doi:10.1038/ng0495-432
Abstract + references | PDF
(758K)
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Somatic mutations in the BRCA1 gene in sporadic ovarian tumours pp439 - 443
Sofia D. Merajver, Trinh M. Pham, Rosemarie F. Caduff, Martha Chen, Ellen L. Poy, Kathleen A. Cooney, Barbara L. Weber, Francis S. Collins, Carolyn Johnston
& Thomas S. Frank
doi:10.1038/ng0495-439
Abstract + references | PDF
(557K)
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Decreased expression of BRCA1 accelerates growth and is often present during sporadic breast cancer progression pp444 - 450
Marilyn E. Thompson, Roy A. Jensen, Patrice S. Obermiller, David L. Page
& Jeffrey T. Holt
doi:10.1038/ng0495-444
Abstract + references | PDF
(769K)
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| Errata | Top |
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Erratum: The Sjögren−Larsson Syndrome gene is close to D17S805 as determined by linkage analysis and allelic association p451
doi:10.1038/ng0495-451a
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(73K)
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Erratum: Characteristics of imprinted genes p451
doi:10.1038/ng0495-451b
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(73K)
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| Corrections | Top |
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Corrigendum: Jackson−Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2 p451
doi:10.1038/ng0495-451c
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(73K)
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Corrigendum: Rescue of neurophysiological phenotype seen in PRP null mice by transgene encoding human prion protein p451
doi:10.1038/ng0495-451d
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(73K)
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Corrigendum: The Wilson disease gene: spectrum of mutations and their consequences p451
doi:10.1038/ng0495-451e
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(73K)
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