De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosispp311 - 312 Carol L. Freund, Qing-Ling Wang, Shiming Chen, Brenda L. Muskat, Carmella D. Wiles, Val C. Sheffield, Samuel G. Jacobson, Roderick R. Mclnnes, Donald J. Zack
& Edwin M. Stone doi:10.1038/ng0498-311 References|PDF
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Predicting functions from protein sequences—where are the bottlenecks?pp313 - 318 Peer Bork
& Eugene V. Koonin doi:10.1038/ng0498-313 Abstract + references|PDF
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A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosispp319 - 324 Margaret Town, Geneviève Jean, Stèphanie Cherqui, Marlene Attard, Lionel Forestier, Scott A. Whitmore, David F. Callen, Olivier Gribouval, Michel Broyer, Gillian P. Bates, William van't Hoff
& Corinne Antignac doi:10.1038/ng0498-319 Abstract + references|PDF
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Human gene targeting by viral vectorspp325 - 330 David W. Russell
& Roll K. Hirata doi:10.1038/ng0498-325 Abstract + references|PDF
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Association of SET domain and myotubularin-related proteins modulates growth controlpp331 - 337 Xiangmin Cui, Immaculata De Vivo, Robert Slany, Alison Miyamoto, Ron Firestein
& Michael L. Cleary doi:10.1038/ng0498-331 Abstract + references|PDF
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A microsatellite genetic linkage map for zebrafish (Danio rerio)pp338 - 343 Ela W. Knapik, Alec Goodman, Marc Ekker, Mario Chevrette, Jonathan Delgado, Stephan Neuhauss, Nobuyoshi Shimoda, Wolfgang Driever, Mark C. Fishman
& Howard J. Jacob doi:10.1038/ng0498-338 Abstract + references|PDF
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Vertebrate genome evolution and the zebrafish gene mappp345 - 349 John H. Postlethwait, Yi-Lin Yan, Michael A. Gates, Sally Horne, Angel Amores, Alison Brownlie, Adriana Donovan, Elizabeth S. Egan, Allan Force, Zhiyuan Gong, Carole Goutel, Andreas Fritz, Robert Kelsh, Ela Knapik, Eric Liao, Barry Paw, David Ransom, Amy Singer, Margaret Thomson, Tariq S. Abduljabbar, Pam Yelick, Dave Beier, J.-S. Joly, Dan Larhammar, Frederic Rosa, Monte Westerfield, Leonard I. Zon, Steve L. Johnson
& William S. Talbot doi:10.1038/ng0498-345 Abstract + references|PDF
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A tRNA suppressor mutation in human mitochondriapp350 - 353 Abdellatif El Meziane, Sanna K. Lehtinen, Nicole Hance, Leo G. J. Nijtmans, Donald Dunbar, Ian J. Holt
& Howard T. Jacobs doi:10.1038/ng0498-350 Abstract + references|PDF
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Neurofibromatosis 2 tumour suppressor schwannomin interacts with II-spectrinpp354 - 359 Daniel R. Scoles, Duong P. Huynh, Paul A. Morcos, Eric R. Coulsell, Nicole G.G. Robinson, Fuyuhiko Tamanoi
& Stefan M. Pulst doi:10.1038/ng0498-354 Abstract + references|PDF
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Loss of E2F-1 reduces tumorigenesis and extends the lifespan of Rb1(+/-) micepp360 - 364 Lili Yamasaki, Roderick Bronson, Bart O. Williams, Nicholas J. Dyson, Ed Harlow
& Tyler Jacks doi:10.1038/ng0498-360 Abstract + references|PDF
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Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophypp365 - 368 Carlo Minetti, Federica Sotgia, Claudio Bruno, Paolo Scartezzini, Paolo Broda, Massimo Bado, Emiliana Masetti, Michela Mazzocco, Aliana Egeo, Maria Alice Donati, Daniela Volonté, Ferruccio Galbiati, Giuseppe Cordone, Franca Dagna Bricarelli, Michael P. Lisanti
& Federico Zara doi:10.1038/ng0498-365 Abstract + references|PDF
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Linkage of familial combined hyperlipidaemia to chromosome 1q21−q23pp369 - 373 Päivi Pajukanta, Ilpo Nuotio, Joseph D. Terwilliger, Kimmo V.K. Porkka, Kati Ylitalo, Jussi Pihlajamäki, Aki J. Suomalainen, Ann-Christine Syvänen, Terho Lehtimäki, Jorma S.A. Viikari, Markku Laakso, Marja-Riitta Taskinen, Christian Ehnholm
& Leena Peltonen doi:10.1038/ng0498-369 Abstract + references|PDF
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Mapping a gene for combined hyperlipidaemia in a mutant mouse strainpp374 - 377 Lawrence W. Castellani, Ari Weinreb, Jackie Bodnar, Aimie M. Goto, Mark Doolittle, Margarete Mehrabian, Peter Demant
& Aldons J. Lusis doi:10.1038/ng0498-374 Abstract + references|PDF
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Ribozyme-mediated trans-splicing of a trinucleotide repeatpp378 - 381 Leonidas A. Phylactou, Charlotte Darrah
& Matthew J.A. Wood doi:10.1038/ng0498-378 Abstract + references|PDF
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Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathiespp382 - 384 Laura E. Warner, Pedro Mancias, Ian J. Butler, Craig M. McDonald, Laura Keppen, K. Gene Koob
& James R. Lupski doi:10.1038/ng0498-382 Abstract + references|PDF
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Chimaeric analysis reveals role of Pdgf receptors in all muscle lineagespp385 - 388 Jeff R. Crosby, Ronald A. Seifert, Philippe Soriano
& Daniel F. Bowen-Pope doi:10.1038/ng0498-385 Abstract + references|PDF
(652K)
II-spectrin
