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The glittering prize pp105 - 106
doi:10.1038/ng1094-105
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(319K)
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| News and Views | Top |
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Visualizing tumour amplification pp107 - 108
Daniel Pinkel
doi:10.1038/ng1094-107
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(256K)
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Identifying complex disease genes: progress and paradigms pp108 - 110
Glenys Thomson
doi:10.1038/ng1094-108
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(373K)
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On the pulse of genetic cardiology pp110 - 111
Ketty Schwartz
doi:10.1038/ng1094-110
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(218K)
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Ion channel Shake-down pp111 - 112
Louis Ptá ek
doi:10.1038/ng1094-111
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(304K)
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| Correspondence | Top |
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Exclusion of HRAS from long QT locus pp113 - 114
Noémi Roy, Pascal Kahlem, Eric Dausse, Mohammed Bennaceur, Sabine Fauré, Jean Weissenbach, Michel Komajda, Isabelle Denjoy, Philippe Coumel, Ketty Schwartz
& Pascale Guicheney
doi:10.1038/ng1094-113
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(289K)
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Predicting the total number of human genes p114
Francisco Antequera
& Adrian Bird
doi:10.1038/ng1094-114a
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(103K)
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Reply to — Predicting the total number of human genes p114
Chris Fields, Mark D Adams, Owen White
& J. Craig Venter
doi:10.1038/ng1094-114b
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(103K)
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Alzheimer's disease and the family effect p115
Gail Pairitz Jarvik
& Ellen M. Wijsman
doi:10.1038/ng1094-115a
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(97K)
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Reply to — Alzheimer's disease and the family effect p115
C. van Duijn
& C. Van Broeckhoven
doi:10.1038/ng1094-115b
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(97K)
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| Review | Top |
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The costs of human inbreeding and their implications for variations at the DNA level pp117 - 121
Alan H. Bittles
& James V. Neel
doi:10.1038/ng1094-117
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(510K)
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| Articles | Top |
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Isolation and characterization of mutations in the human holocarboxylase synthetase cDNA pp122 - 128
Yoichi Suzuki, Yoko Aoki, Yoshinori Ishida, Yasushi Chiba, Akihiro Iwamatsu, Tatsuya Kishino, Norio Niikawa, Yoichi Matsubara
& Kuniaki Narisawa
doi:10.1038/ng1094-122
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(844K)
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Normal long bone growth and development in type X collagen-null mice pp129 - 135
Rita Rosati, Gerald S. B. Horan, Gerald J. Pinero, Silvio Garofalo, Douglas R. Keene, William A. Horton, Eero Vuorio, Benoit de Crombrugghe
& Richard R. Behringer
doi:10.1038/ng1094-129
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(1,295K)
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Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1 pp136 - 140
David L. Browne, Stephen T. Gancher, John G. Nutt, Ewout R. P. Brunt, Eric A. Smith, Patricia Kramer
& Michael Litt
doi:10.1038/ng1094-136
Abstract + references | PDF
(494K)
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Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity pp141 - 147
Changan Jiang, Donald Atkinson, Jeffrey A. Towbin, Igor Splawski, Michael H. Lehmann, Hua Li, Katherine Timothy, R. Thomas Taggart, Peter J. Schwartz, G. Michael Vincent, Arthur J. Moss
& Mark T. Keating
doi:10.1038/ng1094-141
Abstract + references | PDF
(687K)
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Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain pp148 - 154
Michael G. Kaplitt, Paola Leone, Richard J. Samulski, Xiao Xiao, Donald W. Pfaff, Karen L. O'Malley
& Matthew J. During
doi:10.1038/ng1094-148
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(799K)
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Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection pp155 - 161
Xin-Yuan Guan, Paul S. Meltzer, William S. Dalton
& Jeffrey M. Trent
doi:10.1038/ng1094-155
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(864K)
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Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism pp162 - 170
Darren G. Monckton, Rita Neumann, Tara Guram, Neale Fretwell, Keiji Tamaki, Annette MacLeod
& Alec J. Jeffreys
doi:10.1038/ng1094-162
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(1,081K)
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Release of an inhibitor of angiogenesis upon induction of wild type p53 expression in glioblastoma cells pp171 - 176
Erwin G. Van Meir, Peter J. Polverini, Victoria R. Chazin, H.-J. Su Huang, Nicolas de Tribolet
& Webster K. Cavenee
doi:10.1038/ng1094-171
Abstract + references | PDF
(731K)
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Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA) pp177 - 182
Shigeo Nagafuchi, Hiroko Yanagisawa, Emiko Ohsaki, Takefumi Shirayama, Keiko Tadokoro, Tadashi Inoue
& Masao Yamada
doi:10.1038/ng1094-177
Abstract + references | PDF
(619K)
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Maintenance of an open reading frame as an additional level of scrutiny during splice site selection pp183 - 188
Harry C. Dietz
& Raymond J. Kendzior Jr.
doi:10.1038/ng1094-183
Abstract + references | PDF
(726K)
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A locus on chromosome 15q26 (IDDM3) produces susceptibility to insulin-dependent diabetes mellitus pp189 - 194
L. Leigh Field, Rose Tobias
& Tim Magnus
doi:10.1038/ng1094-189
Abstract + references | PDF
(600K)
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Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locus pp195 - 202
Stephen G. Kaler, Linda K. Gallo, Virginia K. Proud, Alan K. Percy, Yvonne Mark, Neil A. Segal, David S. Goldstein, Courtney S. Holmes
& William A. Gahl
doi:10.1038/ng1094-195
Abstract + references | PDF
(946K)
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| Errata | Top |
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Erratum: PAX6 gene dosage effect in a family with congential cataracts, aniridia, anophthalmia and central nervous system defects p203
doi:10.1038/ng1094-203a
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(63K)
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Erratum: Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour p203
doi:10.1038/ng1094-203b
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(63K)
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Erratum: Studying human mutations by sperm typing: instability of CAG trinucleotide repeats in the human androgen receptor gene p203
doi:10.1038/ng1094-203c
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(63K)
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