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| Editorial |  Top |
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Getting hip to the chip pp195 - 197
doi:10.1038/ng0398-195
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(601K)
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| News and Views | Top |
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An essential guide to mtDNA maintenance pp199 - 200
Doug M. Turnbull
& Robert N. Lightowlers
doi:10.1038/ng0398-199
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(322K)
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Who needs genetic markers? pp200 - 202
Leonid Kruglyak
& Linda McAllister
doi:10.1038/ng0398-200
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(379K)
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Every sperm is sacred—or is it? pp202 - 204
Robert E. Braun
doi:10.1038/ng0398-202
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(480K)
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Improbable truth in human MHC diversity? pp204 - 206
Naoyuki Takahata
& Yoko Satta
doi:10.1038/ng0398-204
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(496K)
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Competitive edge at the imprinted Prader-Willi/Angelman region? pp206 - 208
Shirley M. Tilghman, Tamara Caspary
& Robert S. Ingram
doi:10.1038/ng0398-206
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(388K)
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Getting more from your sequences using the web p209
Elizabeth A. Greene
& Steven Henikoff
doi:10.1038/ng0398-209a
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(145K)
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Networking nomenclature p209
Julia White, Lois Maltais
& Daniel Nebert
doi:10.1038/ng0398-209b
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(145K)
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Touching base p210
doi:10.1038/ng0398-210
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(155K)
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| Correspondence | Top |
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Bleomycin hydrolase is associated with risk of sporadic Alzheimer's disease pp211 - 212
Susana E. Montoya, Christopher E. Aston, Steven T. DeKosky, M. Ilyas Kamboh, John S. Lazo
& Robert E. Ferrell
doi:10.1038/ng0398-211
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(235K)
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Escape from X inactivation of Smcx is preceded by silencing during mouse development pp212 - 213
Patricia A. Lingenfelter, David A. Adler, Diane Poslinski, Sushma Thomas, Rosemary W. Elliott, Verne M. Chapman
& Christine M. Disteche
doi:10.1038/ng0398-212
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(232K)
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A leptin missense mutation associated with hypogonadism and morbid obesity pp213 - 215
Andreas Strobel, Tarik Issad, Luc Camoin, Metin Ozata
& A. Donny Strosberg
doi:10.1038/ng0398-213
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(354K)
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A mutation in PDS causes non-syndromic recessive deafness pp215 - 217
Xiaoyan C. Li, Lorraine A. Everett, Anil K. Lalwani, Dilip Desmukh, Thomas B. Friedman, Eric D. Green
& Edward R. Wilcox
doi:10.1038/ng0398-215
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(367K)
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| Articles | Top |
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A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis pp219 - 224
Laura N. Bull, Michiel J.T. van Eijk, Ludmila Pawlikowska, Joseph A. DeYoung, Jenneke A. Juijn, Mira Liao, Leo W.J. Klomp, Noureddine Lomri, Ruud Berger, Bruce R. Scharschmidt, Alexander S. Knisely, Roderick H.J. Houwen
& Nelson B. Freimer
doi:10.1038/ng0398-219
Abstract + references | PDF
(799K)
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Linkage-disequilibrium mapping without genotyping pp225 - 230
Vivian G. Cheung, Jeffrey P. Gregg, Kathryn J. Gogolin-Ewens, Jonathan Bandong, Charles A. Stanley, Lester Baker, Michael J. Higgins, Norma J. Nowak, Thomas B. Shows, Warren J. Ewens, Stanley F. Nelson
& Richard S. Spielman
doi:10.1038/ng0398-225
Abstract + references | PDF
(683K)
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Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in mice pp231 - 236
Nils-Göran Larsson, Jianming Wang, Hans Wilhelmsson, Anders Oldfors, Pierre Rustin, Mark Lewandoski, Gregory S. Barsh
& David A. Clayton
doi:10.1038/ng0398-231
Abstract + references | PDF
(825K)
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Recent origin of HLA-DRB1 alleles and implications for human evolution pp237 - 242
Tomas F. Bergström, Agnetha Josefsson, Henry A. Erlich
& Ulf Gyllensten
doi:10.1038/ng0398-237
Abstract + references | PDF
(701K)
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Distribution of olfactory receptor genes in the human genome pp243 - 250
Sylvie Rouquier, Sylvie Taviaux, Barbara J. Trask, Véronique Brand-Arpon, Ger van den Engh, Jacques Demaille
& Dominique Giorgi
doi:10.1038/ng0398-243
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(1,511K)
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| Letters | Top |
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Testicular degeneration in Bclw-deficient mice pp251 - 256
Andrea J. Ross, Katrina G. Waymire, Julie E. Moss, A.F. Parlow, Michael K. Skinner, Lonnie D. Russell
& Grant R. MacGregor
doi:10.1038/ng0398-251
Abstract + references | PDF
(1,120K)
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The meiotic checkpoint monitoring sypapsis eliminates spermatocytes via p53-independent apoptosis pp257 - 261
Teresa Odorisio, Tristan A. Rodriguez, Edward P. Evans, Alan R. Clarke
& Paul S. Burgoyne
doi:10.1038/ng0398-257
Abstract + references | PDF
(777K)
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A susceptibility locus for Parkinson's disease maps to chromosome 2p13 pp262 - 265
Thomas Gasser, Bertram Müller-Myhsok, Zbigniew K. Wszolek, Ralph Oehlmann, Donald B. Calne, Vincenzo Bonifati, Benjamin Bereznai, Edito Fabrizio, Peter Vieregge
& Rolf D. Horstmann
doi:10.1038/ng0398-262
Abstract + references | PDF
(540K)
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Heart and extra-embryonic mesodermal defects in mouse embryos lacking the bHLH transcription factor Hand1 pp266 - 270
Anthony B. Firulli, David G. McFadden, Qing Lin, Deepak Srivastava
& Eric N. Olson
doi:10.1038/ng0398-266
Abstract + references | PDF
(811K)
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The Hand1 bHLH transcription factor is essential for placentation and cardiac morphogenesis pp271 - 275
Pual Riley, Lynn Anaon-Cartwight
& James C. Cross
doi:10.1038/ng0398-271
Abstract + references | PDF
(764K)
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Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DMA mismatch repair pp276 - 279
Tomas A. Prolla, Sean M. Baker, Allie C. Harris, Jen-Lan Tsao, Xiang Yao, C. Eric Bronner, Binhai Zheng, Melissa Gordon, Jeffrey Reneker, Norman Arnheim, Darryl Shibata, Allan Bradley
& R. Michael Liskay
doi:10.1038/ng0398-276
Abstract + references | PDF
(515K)
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An intramolecular SH3-domain interaction regulates c-Abl activity pp280 - 282
Daniela Barilá
& Giulio Superti-Furga
doi:10.1038/ng0398-280
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(373K)
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Epistatic relationship between Waardenburg Syndrome genes MITF and PAX3 pp283 - 286
Atsushi Watanabe, Kazuhisa Takeda, Barbara Ploplis
& Masayoshi Tachibana
doi:10.1038/ng0398-283
Abstract + references | PDF
(590K)
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Peg3/Pw1 is an imprinted gene involved in the TNF-NF B signal transduction pathway pp287 - 291
Frédéric Relaix, Xiao-Jun Wei, Xiangwei Wu
& David A. Sassoon
doi:10.1038/ng0398-287
Abstract + references | PDF
(680K)
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Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21−22 pp292 - 295
John M. Peters, Robert Barnes, Lynda Bennett, William M. Gitomer, Anne M. Bowcock
& Abhimanyu Garg
doi:10.1038/ng0398-292
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(422K)
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| Marketplace | Top |
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Colour your life In the lab p296
doi:10.1038/ng0398-296
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(170K)
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| Errata | Top |
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Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome p298
doi:10.1038/ng0398-298a
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(139K)
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Atm selectively regulates distinct p53-dependent cell-cycle checkpoint and apoptotic pathways p298
doi:10.1038/ng0398-298b
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(139K)
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| Corrections | Top |
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Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity p298
doi:10.1038/ng0398-298c
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(139K)
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Localisation of a gene implicated in a severe speech and language disorder p298
doi:10.1038/ng0398-298d
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(139K)
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