The value of isolated populationspp309 - 310 Sagiv Shifman
& Ariel Darvasi doi:10.1038/91060 Full text|PDF
(89K)
DelBank: a mouse ES-cell resource for generating deletionspp310 - 311 Neal C. Goodwin, Yasumasa Ishida, Suzanne Hartford, Cate Wnek, Rebecca A. Bergstrom, Philip Leder
& John C. Schimenti doi:10.1038/91064 Full text|PDF
(96K)
Regulating use of stem cellsp312 Liam Donaldson doi:10.1038/91068 Full text|PDF
(22K)
Mutation of DNASE1 in people with systemic lupus erythematosuspp313 - 314 Koji Yasutomo, Takahiko Horiuchi, Shoji Kagami, Hiroshi Tsukamoto, Chinami Hashimura, Maki Urushihara
& Yasuhiro Kuroda doi:10.1038/91070 Abstract|Full text|PDF
(185K)
|Supplementary Information
IBD sharing around the PPARG locus is not increased in dizygotic twins or their mothersp315 David Duffy, Grant Montgomery, Susan Treloar, Andrew Birley, Katherine Kirk, Dorret Boomsma, Leo Beem, Eco de Geus, Eline Slagboom, Joharna Knighton, Peter Reed
& Nicholas Martin doi:10.1038/91074 Abstract|Full text|PDF
(37K)
Photo-mediated gene activation using caged RNA/DNA in zebrafish embryospp317 - 325 Hideki Ando, Toshiaki Furuta, Roger Y. Tsien
& Hitoshi Okamoto Published online: 23 July 2001|doi:10.1038/ng583 Abstract|Full text|PDF
(829K)
|Supplementary Information
CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locuspp335 - 343 Galina N. Filippova, Cortlandt P. Thienes, Bennett H. Penn, Diane H. Cho, Ying Jia Hu, James M. Moore, Todd R. Klesert, Victor V. Lobanenkov
& Stephen J. Tapscott Published online: 23 July 2001|doi:10.1038/ng570 Abstract|Full text|PDF
(1,052K)
A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndromepp345 - 349 Bing Zhou, Shawn K. Westaway, Barbara Levinson, Monique A. Johnson, Jane Gitschier
& Susan J. Hayflick Published online: 23 July 2001|doi:10.1038/ng572 Abstract|Full text|PDF
(836K)
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Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseasepp350 - 354 Andrew R.J. Curtis, Constanze Fey, Christopher M Morris, Laurence A. Bindoff, Paul G. Ince, Patrick F. Chinnery, Alan Coulthard, Margaret J. Jackson, Andrew P. Jackson, Duncan P. McHale, David Hay, William A. Barker, Alex F. Markham, David Bates, Ann Curtis
& John Burn Published online: 02 July 2001|doi:10.1038/ng571 Abstract|Full text|PDF
(1,237K)
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Aromatic hydrocarbon receptor-driven Bax gene expression is required for premature ovarian failure caused by biohazardous environmental chemicalspp355 - 360 Tiina Matikainen, Gloria I. Perez, Andrea Jurisicova, James K. Pru, Jennifer J. Schlezinger, Heui-Young Ryu, Jarmo Laine, Toshiyuki Sakai, Stanley J. Korsmeyer, Robert F. Casper, David H. Sherr
& Jonathan L. Tilly Published online: 16 July 2001|doi:10.1038/ng575 Abstract|Full text|PDF
(1,151K)
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Experimentally-derived haplotypes substantially increase the efficiency of linkage disequilibrium studiespp361 - 364 Julie A. Douglas, Michael Boehnke, Elizabeth Gillanders, Jeffrey M. Trent
& Stephen B. Gruber Published online: 09 July 2001|doi:10.1038/ng582 Abstract|Full text|PDF
(187K)
Identification of the gene altered in Berardinelli−Seip congenital lipodystrophy on chromosome 11q13pp365 - 370 Jocelyne Magré, Marc Delépine, Eliane Khallouf, Tobias Gedde-Dahl Jr, Lionel Van Maldergem, Eric Sobel, Jeanette Papp, Muriel Meier, André Mégarbané, Mark Lathrop
& Jacqueline Capeau Published online: 23 July 2001|doi:10.1038/ng585 Abstract|Full text|PDF
(553K)
|Supplementary Information
Imprinted X inactivation maintained by a mouse Polycomb group genepp371 - 375 Jianbo Wang, Jesse Mager, Yijing Chen, Elizabeth Schneider, James C. Cross, Andras Nagy
& Terry Magnuson Published online: 23 July 2001|doi:10.1038/ng574 Abstract|Full text|PDF
(603K)
Mutation of a new gene causes a unique form of Hermansky−Pudlak syndrome in a genetic isolate of central Puerto Ricopp376 - 380 Yair Anikster, Marjan Huizing, James White, Yuriy O. Shevchenko, Diana L. Fitzpatrick, Jeffrey W. Touchman, John G. Compton, Sherri J. Bale, Richard T. Swank, William A. Gahl
& Jorge R. Toro Published online: 16 July 2001|doi:10.1038/ng576 Abstract|Full text|PDF
(985K)
|Supplementary Information
Mutations in the gene encoding B, a novel transporter protein, reduce melanin content in medakapp381 - 385 Shoji Fukamachi, Atsuko Shimada
& Akihiro Shima Published online: 23 July 2001|doi:10.1038/ng584 Abstract|Full text|PDF
(259K)
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Mutations in IHH, encoding Indian hedgehog, cause brachydactyly type A-1pp386 - 388 Bo Gao, Jingzhi Guo, Chaowen She, Anli Shu, Maosheng Yang, Zheng Tan, Xinping Yang, Shengzhen Guo, Guoying Feng
& Lin He Published online: 16 July 2001|doi:10.1038/ng577 Abstract|Full text|PDF
(341K)
Increased efficiency of mRNA 3' end formation: a new genetic mechanism contributing to hereditary thrombophiliapp389 - 392 Niels H. Gehring, Ute Frede, Gabriele Neu-Yilik, Patrick Hundsdoerfer, Barbara Vetter, Matthias W. Hentze
& Andreas E. Kulozik Published online: 09 July 2001|doi:10.1038/ng578 Abstract|Full text|PDF
(215K)
Mutations in the region encoding the von Willebrand factor A domain of matrilin-3 are associated with multiple epiphyseal dysplasiapp393 - 396 Kathryn L. Chapman, Geert R. Mortier, Kay Chapman, John Loughlin, Michael E. Grant
& Michael D. Briggs Published online: 02 July 2001|doi:10.1038/ng573 Abstract|Full text|PDF
(833K)
|Supplementary Information
