Establishment of a gene-trap sequence tag library to generate mutant
mice from embryonic stem cellspp13 - 14 Michael V. Wiles, Franz Vauti, Jürgen Otte, Ernst-Martin Füchtbauer, Patricia Ruiz, Annette Füchtbauer, Hans-Henning Arnold, Hans Lehrach, Thomas Metz, Harald von Melchner
& Wolfgang Wurst doi:10.1038/71622 Full text|PDF
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The Fanconi anaemia gene FANCF encodes a novel protein with homology
to ROMpp15 - 16 Johan P. de Winter, Martin A. Rooimans, Laura van der Weel, Carola G.M. van Berkel, Noa Alon, Lucine Bosnoyan-Collins, Jan de Groot, Yu Zhi, Quinten Waisfisz, Jan C. Pronk, Fré Arwert, Christopher G. Mathew, Rik J. Scheper, Maureen E. Hoatlin, Manuel Buchwald
& Hans Joenje doi:10.1038/71626 Abstract|Full text|PDF
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Telomerase prevents the accelerated cell ageing of Werner syndrome fibroblasts
pp16 - 17 Fiona S. Wyllie, Christopher J. Jones, Julia W. Skinner, Michele F. Haughton, Corrin Wallis, David Wynford-Thomas, Richard G.A. Faragher
& David Kipling doi:10.1038/71630 Abstract|Full text|PDF
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Mutation of PAX9 is associated with oligodontiapp18 - 19 David W. Stockton, Parimal Das, Monica Goldenberg, Rena N. D'Souza
& Pragna I. Patel doi:10.1038/71634 Abstract|Full text|PDF
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Genealogies of mouse inbred strainspp23 - 25 Jon A. Beck, Sarah Lloyd, Majid Hafezparast, Moyha Lennon-Pierce, Janan T. Eppig, Michael F.W. Festing
& Elizabeth M.C. Fisher doi:10.1038/71641 Abstract|Full text|PDF
(107K)
|Supplementary Information
MLH3: a DNA mismatch repair gene associated with mammalian microsatellite
instabilitypp27 - 35 Steven M. Lipkin, Victoria Wang, Russell Jacoby, Sharmila Banerjee-Basu, Andreas D. Baxevanis, Henry T. Lynch, Rosemary M. Elliott
& Francis S. Collins doi:10.1038/71643 Abstract|Full text|PDF
(1,089K)
|Supplementary Information See also:News and Views by Jiricny
Mutations in TNFRSF11A, affecting the signal peptide of RANK,
cause familial expansile osteolysispp45 - 48 Anne E. Hughes, Stuart H. Ralston, John Marken, Christine Bell, Heather MacPherson, Richard G.H. Wallace, Wim van Hul, Michael P. Whyte, Kyoshi Nakatsuka, Louis Hovy
& Dirk M. Anderson doi:10.1038/71667 Abstract|Full text|PDF
(384K)
Efficient lentiviral transduction of liver requires cell cycling
in vivopp49 - 52 Frank Park, Kazuo Ohashi, Winnie Chiu, Luigi Naldini
& Mark A. Kay doi:10.1038/71673 Abstract|Full text|PDF
(542K)
See also:News and Views by Emerman
Novel dominant mutations in Saccharomyces cerevisiae MSH6pp53 - 56 Ruchira Das Gupta
& Richard D. Kolodner doi:10.1038/71684 Abstract|Full text|PDF
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Reversibility of acute B-cell leukaemia induced by BCR−ABL1pp57 - 60 Claudia S. Huettner, Pu Zhang, Richard A. Van Etten
& Daniel G. Tenen doi:10.1038/71691 Abstract|Full text|PDF
(447K)
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey
diseasepp61 - 65 Zhilan Hu, Jeannette M. Bonifas, Jenna Beech, Graham Bench, Takako Shigihara, Hideoki Ogawa, Shigaku Ikeda, Theodora Mauro
& Ervin H. Epstein Jr doi:10.1038/71701 Abstract|Full text|PDF
(840K)
A mouse model for spinal muscular atrophypp66 - 70 Hsiu Mei Hsieh-Li, Jan-Gowth Chang, Yuh-Jyh Jong, Mei-Hsiang Wu, Nancy M. Wang, Chang Hai Tsai
& Hung Li doi:10.1038/71709 Abstract|Full text|PDF
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Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal
syndrome type Ipp71 - 74 Parastoo Momeni, Gernot Glöckner, Olaf Schmidt, Diane von Holtum, Beate Albrecht, Gabriele Gillessen-Kaesbach, Raoul Hennekam, Peter Meinecke, Bernhard Zabel, André Rosenthal, Bernhard Horsthemke
& Hermann-Josef Lüdecke doi:10.1038/71717 Abstract|Full text|PDF
(430K)
Cardiac defects and renal failure in mice with targeted mutations in Pkd2pp75 - 78 Guanqing Wu, Glen S. Markowitz, Li Li, Vivette D. D'Agati, Stephen M. Factor, Lin Geng, Sonia Tibara, Jay Tuchman, Yiqiang Cai, Jong Hoon Park, Janet van Adelsberg, Harry Hou Jr, Raju Kucherlapati, Winfried Edelmann
& Stefan Somlo doi:10.1038/71724 Abstract|Full text|PDF
(1,473K)
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital
amaurosispp79 - 83 Melanie M. Sohocki, Sara J. Bowne, Lori S. Sullivan, Seth Blackshaw, Constance L. Cepko, Annette M. Payne, Shomi S. Bhattacharya, Shagufta Khaliq, S. Qasim Mehdi, David G. Birch, Wilbur R. Harrison, Frederick F.B. Elder, John R. Heckenlively
& Stephen P. Daiger doi:10.1038/71732 Abstract|Full text|PDF
(988K)
Molecular mechanism for duplication 17p11.2— the homologous recombination
reciprocal of the Smith-Magenis microdeletionpp84 - 87 Lorraine Potocki, Ken-Shiung Chen, Sung-Sup Park, Doreen E. Osterholm, Marjorie A. Withers, Virginia Kimonis, Anne M. Summers, Wendy S. Meschino, Kwame Anyane-Yeboa, Catherine D. Kashork, Lisa G. Shaffer
& James R. Lupski doi:10.1038/71743 Abstract|Full text|PDF
(283K)
DNA methyltransferase Dnmt1 associates with histone deacetylase activitypp88 - 91 François Fuks, Wendy A. Burgers, Alexander Brehm, Luke Hughes-Davies
& Tony Kouzarides doi:10.1038/71750 Abstract|Full text|PDF
(293K)
Nested chromosomal deletions induced with retroviral vectors in mice
pp92 - 95 Hong Su, Xiaozhong Wang
& Allan Bradley doi:10.1038/71756 Abstract|Full text|PDF
(237K)
