Early death of mice cloned from somatic cellspp253 - 254 Narumi Ogonuki, Kimiko Inoue, Yoshie Yamamoto, Yoko Noguchi, Kentaro Tanemura, Osamu Suzuki, Hiroyuki Nakayama, Kunio Doi, Yukiko Ohtomo, Michiko Satoh, Akira Nishida
& Atsuo Ogura Published online: 11 February 2002|doi:10.1038/ng841 Abstract|Full text|PDF
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A gene-driven approach to the identification of ENU mutants in the mousepp255 - 256 Emma L. Coghill, Alison Hugill, Nick Parkinson, Claire Davison, Peter Glenister, Sian Clements, Jackie Hunter, Roger D. Cox
& Steve D.M. Brown Published online: 19 February 2002|doi:10.1038/ng847 Abstract|Full text|PDF
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Beethoven, a mouse model for dominant, progressive hearing loss DFNA36pp257 - 258 Sarah Vreugde, Alexandra Erven, Corné J. Kros, Walter Marcotti, Helmut Fuchs, Kiyoto Kurima, Edward R. Wilcox, Thomas B. Friedman, Andrew J. Griffith, Rudi Balling, Martin Hrabé de Angelis, Karen B. Avraham
& Karen P. Steel Published online: 19 February 2002|doi:10.1038/ng848 Abstract|Full text|PDF
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The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like proteinpp259 - 269 Christopher J. Ward, Marie C. Hogan, Sandro Rossetti, Denise Walker, Tam Sneddon, Xiaofang Wang, Vicky Kubly, Julie M. Cunningham, Robert Bacallao, Masahiko Ishibashi, Dawn S. Milliner, Vicente E. Torres
& Peter C. Harris Published online: 04 February 2002|doi:10.1038/ng833 Abstract|Full text|PDF
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CEACAM1 regulates insulin clearance in liverpp270 - 276 Matthew N. Poy, Yan Yang, Khadijeh Rezaei, Mats A. Fernström, Abraham D. Lee, Yoshiaki Kido, Sandra K. Erickson
& Sonia M. Najjar Published online: 19 February 2002|doi:10.1038/ng840 Abstract|Full text|PDF
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Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell functionpp277 - 284 Kiyoto Kurima, Linda M. Peters, Yandan Yang, Saima Riazuddin, Zubair M. Ahmed, Sadaf Naz, Deidre Arnaud, Stacy Drury, Jianhong Mo, Tomoko Makishima, Manju Ghosh, P.S.N. Menon, Dilip Deshmukh, Carole Oddoux, Harry Ostrer, Shaheen Khan, Sheikh Riazuddin, Prescott L. Deininger, Lori L. Hampton, Susan L. Sullivan, James F. Battey Jr., Bronya J.B. Keats, Edward R. Wilcox, Thomas B. Friedman
& Andrew J. Griffith Published online: 19 February 2002|doi:10.1038/ng842 Abstract|Full text|PDF
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BRCA1 regulates the G2/M checkpoint by activating Chk1 kinase upon DNA damagepp285 - 289 Ronit I. Yarden, Sherly Pardo-Reoyo, Magda Sgagias, Kenneth H. Cowan
& Lawrence C. Brody Published online: 11 February 2002|doi:10.1038/ng837 Abstract|Full text|PDF
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The DNA damage-dependent intra−S phase checkpoint is regulated by parallel pathwayspp290 - 294 Jacob Falck, John H.J. Petrini, Bret R. Williams, Jiri Lukas
& Jiri Bartek Published online: 19 February 2002|doi:10.1038/ng845 Abstract|Full text|PDF
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|Supplementary Information
Inflammatory reactions and severe neutropenia in mice lacking the transcriptional repressor Gfi1pp295 - 300 Holger Karsunky, Hui Zeng, Thorsten Schmidt, Branko Zevnik, Reinhart Kluge, Kurt Werner Schmid, Ulrich Dührsen
& Tarik Möröy Published online: 28 January 2002|doi:10.1038/ng831 Abstract|Full text|PDF
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Molecular characterization of inter-telomere and intra-telomere mutations in human ALT cellspp301 - 305 Helen Varley, Hilda A. Pickett, Jennifer L. Foxon, Roger R. Reddel
& Nicola J. Royle Published online: 04 February 2002|doi:10.1038/ng834 Abstract|Full text|PDF
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A mutant PTH/PTHrP type I receptor in enchondromatosispp306 - 310 Sevan Hopyan, Nalan Gokgoz, Raymond Poon, Robert C. Gensure, Chunying Yu, William G. Cole, Robert S. Bell, Harald Jüppner, Irene L. Andrulis, Jay S. Wunder
& Benjamin A. Alman Published online: 19 February 2002|doi:10.1038/ng844 Abstract|Full text|PDF
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Pathogen stress increases somatic recombination frequency in Arabidopsispp311 - 314 Jan M. Lucht, Brigitte Mauch-Mani, Henry-York Steiner, Jean-Pierre Metraux, John Ryals
& Barbara Hohn Published online: 11 February 2002|doi:10.1038/ng846 Abstract|Full text|PDF
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A polymorphic microsatellite that mediates induction of PIG3 by p53pp315 - 320 Ana Contente, Alexandra Dittmer, Manuela C. Koch, Judith Roth
& Matthias Dobbelstein Published online: 04 February 2002|doi:10.1038/ng836 Abstract|Full text|PDF
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Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear genepp321 - 324 Tamio Suzuki, Wei Li, Qing Zhang, Amna Karim, Edward K. Novak, Elena V. Sviderskaya, Simon P. Hill, Dorothy C. Bennett, Alex V. Levin, H. Karel Nieuwenhuis, Chin-To Fong, Claudio Castellan, Bianca Miterski, Richard T. Swank
& Richard A. Spritz Published online: 11 February 2002|doi:10.1038/ng835 Abstract|Full text|PDF
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A bisexually reproducing all-triploid vertebratepp325 - 328 Matthias Stöck, Dunja K. Lamatsch, Claus Steinlein, Jörg T. Epplen, Wolf-Rüdiger Grosse, Robert Hock, Thomas Klapperstück, Kathrin P. Lampert, Ulrich Scheer, Michael Schmid
& Manfred Schartl Published online: 11 February 2002|doi:10.1038/ng839 Abstract|Full text|PDF
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Higher-order structure in pericentric heterochromatin involves a distinct pattern of histone modification and an RNA componentpp329 - 334 Christèle Maison, Delphine Bailly, Antoine H.F.M. Peters, Jean-Pierre Quivy, Danièle Roche, Angela Taddei, Monika Lachner, Thomas Jenuwein
& Geneviève Almouzni Published online: 19 February 2002|doi:10.1038/ng843 Abstract|Full text|PDF
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Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory featurespp335 - 341 Sergey Kalachikov, Oleg Evgrafov, Barbara Ross, Melodie Winawer, Christie Barker-Cummings, Filippo Martinelli Boneschi, Chang Choi, Pavel Morozov, Kamna Das, Elita Teplitskaya, Andrew Yu, Eftihia Cayanis, Graciela Penchaszadeh, Andreas H. Kottmann, Timothy A. Pedley, W. Allen Hauser, Ruth Ottman
& T. Conrad Gilliam Published online: 28 January 2002|doi:10.1038/ng832 Abstract|Full text|PDF
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