Hepatocyte migration during liver development requires Prox1pp254 - 255 Beatriz Sosa-Pineda, Jeffrey T. Wigle
& Guillermo Oliver doi:10.1038/76996 Abstract|Full text|PDF
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Mitochondrial DNA heteroplasmy in cloned cattle produced by fetal and
adult cell cloningpp255 - 257 Ralf Steinborn, Pamela Schinogl, Valeri Zakhartchenko, Roland Achmann, Wolfgang Schernthaner, Miodrag Stojkovic, Eckhard Wolf, Mathias Müller
& Gottfried Brem doi:10.1038/77000 Abstract|Full text|PDF
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|Supplementary Information
ABCR expression in foveal cone photoreceptors and its role in Stargardt
macular dystrophypp257 - 258 Laurie L. Molday, Arnold R. Rabin
& Robert S. Molday doi:10.1038/77004 Abstract|Full text|PDF
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Genetic testing and quality control in diagnostic laboratoriespp259 - 260 Elisabeth Dequeker
& Jean-Jacques Cassiman doi:10.1038/77008 Abstract|Full text|PDF
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Mitotic replication initiation proteins are not required for pre-meiotic S phasepp263 - 268 Susan L. Forsburg
& Jeffrey A. Hodson doi:10.1038/77015 Abstract|Full text|PDF
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DNMT1 binds HDAC2 and a new co-repressor, DMAP1, to form a complex at
replication focipp269 - 277 Michael R. Rountree, Kurtis E. Bachman
& Stephen B. Baylin doi:10.1038/77023 Abstract|Full text|PDF
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Mutations in an oocyte-derived growth factor gene (BMP15) cause increased ovulation rate and infertility in a dosage-sensitive mannerpp279 - 283 Susan M. Galloway, Kenneth P. McNatty, Lisa M. Cambridge, Mika P.E. Laitinen, Jennifer L. Juengel, T. Sakari Jokiranta, Robert J. McLaren, Kaisu Luiro, Ken G. Dodds, Grant W. Montgomery, Anne E. Beattie, George H. Davis
& Olli Ritvos doi:10.1038/77033 Abstract|Full text|PDF
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Social amnesia in mice lacking the oxytocin genepp284 - 288 Jennifer N. Ferguson, Larry J. Young, Elizabeth F. Hearn, Martin M. Matzuk, Thomas R. Insel
& James T. Winslow doi:10.1038/77040 Abstract|Full text|PDF
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Genetic basis of total colourblindness among the Pingelapese islanders
pp289 - 293 Olof H. Sundin, Jun-Ming Yang, Yingying Li, Danping Zhu, Jane N. Hurd, Thomas N. Mitchell, Eduardo D. Silva
& Irene Hussels Maumenee doi:10.1038/77162 Abstract|Full text|PDF
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|Supplementary Information
Gene-expression profile of the ageing brain in micepp294 - 297 Cheol-Koo Lee, Richard Weindruch
& Tomas A. Prolla doi:10.1038/77046 Abstract|Full text|PDF
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Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanismpp298 - 301 Kristiina Avela, Marita Lipsanen-Nyman, Niina Idänheimo, Eva Seemanová, Sally Rosengren, Tomi P. Mäkelä, Jaakko Perheentupa, Albert de la Chapelle
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Restoration of photoreceptor ultrastructure and function in retinal degeneration
slow mice by gene therapypp306 - 310 Robin R. Ali, Gian-Marco Sarra, Clare Stephens, Mahesh de Alwis, James W.B. Bainbridge, Peter M. Munro, Sascha Fauser, Martin B. Reichel, Christine Kinnon, David M. Hunt, Shomi S. Bhattacharya
& Adrian J. Thrasher doi:10.1038/77068 Abstract|Full text|PDF
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The glial cells missing-1 protein is essential for branching morphogenesis in the chorioallantoic placentapp311 - 314 Lynn Anson-Cartwright, Kerri Dawson, Doug Holmyard, Susan J. Fisher, Robert A. Lazzarini
& James C. Cross doi:10.1038/77076 Abstract|Full text|PDF
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Epigenetic inactivation of a RAS association domain family protein from the lung tumour suppressor locus 3p21.3pp315 - 319 Reinhard Dammann, Chun Li, Jung-Hoon Yoon, Philip L. Chin, Steven Bates
& Gerd P. Pfeifer doi:10.1038/77083 Abstract|Full text|PDF
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The genetically isolated populations of Finland and Sardinia may not
be a panacea for linkage disequilibrium mapping of common disease genespp320 - 323 Iain A. Eaves, Tony R. Merriman, Rachael A. Barber, Sarah Nutland, Eva Tuomilehto-Wolf, Jaakko Tuomilehto, Francesco Cucca
& John A. Todd doi:10.1038/77091 Abstract|Full text|PDF
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Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28pp324 - 328 Patricia Taillon-Miller, Irma Bauer-Sardiña, Nancy L. Saccone, Jenna Putzel, Tarja Laitinen, Antonio Cao, Juha Kere, Giuseppe Pilia, John P. Rice
& Pui-Yan Kwok doi:10.1038/77100 Abstract|Full text|PDF
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Syndecan-1 is required for Wnt-1-induced mammary tumorigenesis in micepp329 - 332 Caroline M. Alexander, Frieda Reichsman, Michael T. Hinkes, John Lincecum, Klaus A. Becker, Susan Cumberledge
& Merton Bernfield doi:10.1038/77108 Abstract|Full text|PDF
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Widespread aneuploidy revealed by DNA microarray expression profiling
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& Matthew J. Marton doi:10.1038/77116 Abstract|Full text|PDF
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DNMT1 forms a complex with Rb, E2F1 and HDAC1 and represses transcription from E2F-responsive promoterspp338 - 342 Keith D. Robertson, Slimane Ait-Si-Ali, Tomoki Yokochi, Paul A. Wade, Peter L. Jones
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Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosispp343 - 346 Annalisa Frattini, Paul J. Orchard, Cristina Sobacchi, Silvia Giliani, Mario Abinun, Jan P. Mattsson, David J. Keeling, Ann-Katrin Andersson, Pia Wallbrandt, Luigi Zecca, Luigi D. Notarangelo, Paolo Vezzoni
& Anna Villa doi:10.1038/77131 Abstract|Full text|PDF
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Cell-cycle-regulated association of RAD50/MRE11/NBS1 with TRF2 and human telomerespp347 - 352 Xu-Dong Zhu, Bernhard Küster, Matthias Mann, John H.J. Petrini
& Titia de Lange doi:10.1038/77139 Abstract|Full text|PDF
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A syndrome of tricuspid atresia in mice with a targeted mutation of the gene encoding Fog-2pp353 - 356 Eric C. Svensson, Gordon S. Huggins, Hua Lin, Cynthia Clendenin, Fang Jiang, Rachel Tufts, Fred B. Dardik
& Jeffrey M. Leiden doi:10.1038/77146 Abstract|Full text|PDF
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Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cystspp357 - 361 Juha Paloneva, Marjo Kestilä, Jun Wu, Antti Salminen, Tom Böhling, Vesa Ruotsalainen, Panu Hakola, Alexander B.H. Bakker, Joseph H. Phillips, Petra Pekkarinen, Lewis L. Lanier, Tuomo Timonen
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