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Nature Genetics
ISSUE
July 1998, Volume 19 No 3
Editorial
News and Views
Correspondence
New Technology
Articles
Letters
Corrections
About the cover
Editorial Top
Privacy matters pp207 - 208
doi:10.1038/874
Full text | PDF (50K)
News and Views Top
Weighing in on diabetes risk pp209 - 210
Mark McCarthy
doi:10.1038/876
Full text | PDF (49K)
See also: Letter by Hattersley et al.
Counting on Xist pp211 - 212
Laura Carrel & Huntington F. Willard
doi:10.1038/878
Full text | PDF (138K)
See also: Letter by Clerc & Avner
Sometimes it's hot, sometimes it's not pp213 - 214
Åke Lernmark & Jurg Ott
doi:10.1038/881
Full text | PDF (45K)
See also: Letter by Concannon et al.  | Letter by Mein et al.
Nuclear power and mitochondrial disease pp214 - 215
Salvatore DiMauro & Eric A. Schon
doi:10.1038/883
Full text | PDF (66K)
It's raining SNPs, hallelujah? pp216 - 217
Aravinda Chakravarti
doi:10.1038/885
Full text | PDF (51K)
See also: Article by Nickerson et al.
Touching base p218
doi:10.1038/888
Full text | PDF (78K)
Correspondence Top
Cloning and characterization of a family of novel mammalian DNA (cytosine-5) methyltransferases pp219 - 220
Masaki Okano, Shaoping Xie & En Li
doi:10.1038/890
Full text | PDF (241K)
Non-invasive sexing of preimplantation stage mammalian embryos pp220 - 222
Anna-Katerina Hadjantonakis, Marina Gertsenstein, Masahito Ikawa, Masaru Okabe & Andras Nagy
doi:10.1038/893
Full text | PDF (363K)
Human genome annotation — a possible role for HUGO? p222
Peter Little
doi:10.1038/896
Full text | PDF (37K)
PTEN and inherited hamartoma-cancer syndromes p223
Charis Eng & Monica Peacocke
doi:10.1038/897
Full text | PDF (34K)
New Technology Top
Mutation detection and single-molecule counting using isothermal rolling-circle amplification pp225 - 232
Paul M. Lizardi, Xiaohua Huang, Zhengrong Zhu, Patricia Bray-Ward, David C. Thomas & David C. Ward
doi:10.1038/898
Abstract | Full text | PDF (489K)
Articles Top
DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene pp233 - 240
Deborah A. Nickerson, Scott L. Taylor, Kenneth M. Weiss, Andrew G. Clark, Richard G. Hutchinson, Jari Stengård, Veikko Salomaa, Erkki Vartiainen, Eric Boerwinkle & Charles F. Sing
doi:10.1038/907
Abstract | Full text | PDF (394K)
See also: News and Views by Chakravarti
Identification of the gene responsible for Best macular dystrophy pp241 - 247
Konstantin Petrukhin, Markus J. Koisti, Benjamin Bakall, Wen Li, Guochun Xie, Towa Marknell, Ola Sandgren, Kristina Forsman, Gösta Holmgren, Sten Andreasson, Mihailo Vujic, Arthur A. B. Bergen, Valarie McGarty-Dugan, David Figueroa, Christopher P. Austin, Michael L. Metzker, C.Thomas Caskey & Claes Wadelius
doi:10.1038/915
Abstract | Full text | PDF (376K)
Letters Top
Role of the region 3' to Xist exon 6 in the counting process of X-chromosome inactivation pp249 - 253
Philippe Clerc & Philip Avner
doi:10.1038/924
Abstract | Full text | PDF (185K)
See also: News and Views by Carrel & Willard
BRCA1 protein is linked to the RNA polymerase II holoenzyme complex via RNA helicase A pp254 - 256
Stephen F. Anderson, Brian P. Schlegel, Toshihiro Nakajima, Eric S. Wolpin & Jeffrey D. Parvin
doi:10.1038/930
Abstract | Full text | PDF (290K)
Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel pp257 - 259
Susanne Kohl, Tim Marx, Ian Giddings, Herbert Jägle, Samuel G. Jacobson, Eckhart Apfelstedt-Sylla, Eberhart Zrenner, Lindsay T. Sharpe & Bernd Wissinger
doi:10.1038/935
Abstract | Full text | PDF (251K)
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness pp260 - 263
Tim M. Strom, Gerald Nyakatura, Eckart Apfelstedt-Sylla, Heide Hellebrand, Birgit Lorenz, Bernhard H. F. Weber, Krisztina Wutz, Nadja Gutwillinger, Klaus Rüther, Bernd Drescher, Christian Sauer, Eberhart Zrenner, Thomas Meitinger, Andre Rosenthal & Alfons Meindl
doi:10.1038/940
Abstract | Full text | PDF (455K)
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness  pp264 - 267
N. Torben Bech-Hansen, Margaret J. Naylor, Tracy A. Maybaum, William G. Pearce, Ben Koop, Gerald A. Fishman, Marilyn Mets, Maria A. Musarella & Kym M. Boycott
doi:10.1038/947
Abstract | Full text | PDF (176K)
Mutations in the glucokinase gene of the fetus result in reduced birth weight pp268 - 270
Andrew T. Hattersley, Frances Beards, Elizabeth Ballantyne, Maggie Appleton, Rod Harvey & Sian Ellard
doi:10.1038/953
Abstract | Full text | PDF (51K)
See also: News and Views by McCarthy
Mutation in Npps in a mouse model of ossification of the posterior longitudinal ligament of the spine pp271 - 273
Akihiko Okawa, Isao Nakamura, Sumio Goto, Hideshige Moriya, Yusuke Nakamura & Shiro Ikegawa
doi:10.1038/956
Abstract | Full text | PDF (134K)
The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries pp274 - 278
Kenro Kusumi, Eileen Sun, Anne W. Kerrebrock, Roderick T. Bronson, Dow-Chung Chi, Monique Bulotsky, Jessica B. Spencer, Bruce W. Birren, Wayne N. Frankel & Eric S. Lander
doi:10.1038/961
Abstract | Full text | PDF (394K)
Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I pp279 - 281
David S. Geller, Juan Rodriguez-Soriano, Alfredo V. Boado, Søren Schifter, Milan Bayer, Sue S. Chang & Richard P. Lifton
doi:10.1038/966
Abstract | Full text | PDF (85K)
Renal and intestinal absorptive defects in mice lacking the NHE3 Na +/H+ exchanger pp282 - 285
Patrick J. Schultheis, Lane L. Clarke, Pierre Meneton, Marian L. Miller, Manoocher Soleimani, Lara R. Gawenis, Tara M. Riddle, John J. Duffy, Thomas Doetschman, Tong Wang, Gerhard Giebisch, Peter S. Aronson, John N. Lorenz & Gary E. Shull
doi:10.1038/969
Abstract | Full text | PDF (205K)
CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis pp286 - 288
Minna Savukoski, Tuomas Klockars, Ville Holmberg, Pirkko Santavuori, Eric S. Lander & Leena Peltonen
doi:10.1038/975
Abstract | Full text | PDF (109K)
Loss of adenylyl cyclase I activity disrupts patterning of mouse somatosensory cortex pp289 - 291
Raja M. Abdel-Majid, Wey L. Leong, Leonard C. Schalkwyk, Donald S. Smallman, Scott T. Wong, Daniel R. Storm, Alan Fine, Melanie J. Dobson, Duane L. Guernsey & Paul E. Neumann
doi:10.1038/980
Abstract | Full text | PDF (132K)
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus pp292 - 296
Patrick Concannon, Kathryn J. Gogolin-Ewens, David A. Hinds, Beth Wapelhorst, V. Annem Morrison, Brigid Stirling, Mirna Mitra, Jennifer Farmer, Sloan R. Williams, Nancy J. Cox, Graeme I. Bell, Neil Risch & Richard S. Spielman
doi:10.1038/985
Abstract | Full text | PDF (119K)
See also: News and Views by Lernmark & Ott
A search for type 1 diabetes susceptibility genes in families from the United Kingdom pp297 - 300
CharlesA. Mein, Laura Esposito, Michael G. Dunn, Gillian C. L. Johnson, Andrew E. Timms, Juliet V. Goy, Annabel N. Smith, Liam Sebag-Montefiore, Marilyn E. Merriman, Amanda J. Wilson, Lynn E. Pritchard, Francesco Cucca, Anthony H. Barnett, Stephen C. Bain & John A. Todd
doi:10.1038/991
Abstract | Full text | PDF (68K)
See also: News and Views by Lernmark & Ott
A male-female bias in type 1 diabetes and linkage to chromosome Xp in MHC HLA-DR3-positive patients pp301 - 302
Francesco Cucca, Juliet V. Goy, Yoshihiko Kawaguchi, Laura Esposito, Marilyn E. Merriman, Amanda J. Wilson, Heather J. Cordell, Stephen C. Bain & John A. Todd
doi:10.1038/995
Abstract | Full text | PDF (55K)
Corrections Top
A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element p303
Lawrence Reiter, Tatsufumi Murakami, Thearith Koeuth, Liu Pentao, Donna Muzny, Richard Gibbs & James Lupski
doi:10.1038/998
Abstract | Full text | PDF (48K)
Vertebrate genome evolution and the zebrafish gene map p303
John Postlethwait, Yi-Lin Yan, Michael Gates, Sally Horne, Angel Amores, Alison Brownlie, Adriana Donovan, Elizabeth Egan, Allan Force, Zhiyuan Gong, Carole Goutel, Andreas Fritz, Robert Kelsh, Ela Knapik, Eric Liao, Barry Paw, David Ransom, Amy Singer, Margaret Thomson, Tariq Abduljabbar, Pam Yelick, Dave Beier, Joly, Dan Larhammar, Frederic Rosa, Monte Westerfield, Leonard Zon, Steve Johnson & William Talbot
doi:10.1038/1000
Abstract | Full text | PDF (48K)
Mutations in GDI1 are responsible for X-linked non-specific mental retardation p303
Patrizia D'Adamo, Andrea Menegon, Cristiana Lo Nigro, Marina Grasso, Massimo Gulisano, Filippo Tamanini, Thierry Bienvenu, Agi Gedeon, Ben Oostra, Shih-Kwang Wu, Anurag Tandon, Flavia Valtorta, William Balch, Jamel Chelly & Daniela Toniolo
doi:10.1038/1001
Abstract | Full text | PDF (48K)
  Top
 
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Nature Genetics
ISSN: 1061-4036
EISSN: 1546-1718
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