BRCA1 is localized in cytoplasmic tube-like invaginations in the nucleuspp122 - 124 Elisabeth Coene, Patrick Van Oostveldt, Karen Willems, John van Emmelo
& Christian R. De Potter doi:10.1038/ng0697-122 References|PDF
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Congenital hypothyroidism caused by a mutation in the Na+/l- symporterpp124 - 125 Hirokazu Fujiwara, Ke-ita Tatsumi, Kazunori Miki, Tokuzo Harada, Kiyoshi Miyai, Shin-ichiro Takai
& Nobuyuki Amino doi:10.1038/ng0697-124 References|PDF
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A new dimension for the human genome project: towards comprehensive expression mapspp126 - 132 Tom Strachan, Marc Abitbol, Duncan Davidson
& Jacques S. Beckmann doi:10.1038/ng0697-126 Abstract + references|PDF
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Functional expression and germline atransmission of a human chromosome fragment in chimaeric micepp133 - 143 Kazuma Tomizuka, Hitoshi Yoshida, Hiroshi Uejima, Hiroyuki Kugoh, Kaoru Sato, Atsuko Ohguma, Michiko Hayasaka, Kazunori Hanaoka, Mitsuo Oshimura
& Isao Ishida doi:10.1038/ng0697-133 Abstract + references|PDF
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A functional neo-centromere formed through activation of a latent human centromere and consisting of non-alpha-satellite DNApp144 - 153 Desirée du Sart, Michael R. Cancilla, Elizabeth Earle, Jen-i Mao, Richard Saffery, Kellie M. Tainton, Paul Kalitsis, John Martyn, Alyssa E. Barry
& K. H. Andy Choo doi:10.1038/ng0697-144 Abstract + references|PDF
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Regulation of cardiac mesodermal and neural crest development by the bHLH transcription factor, dHANDpp154 - 160 Deepak Srivastava, Tiffani Thomas, Qing Lin, Margaret L. Kirby, Doris Brown
& Eric N. Olson doi:10.1038/ng0697-154 Abstract + references|PDF
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The BCL-6 proto-oncogene controls germinal-centre formation and Th2-type inflammationpp161 - 170 Bihui H. Ye, Giorgio Cattoretti, Qiong Shen, Jiandong Zhang, Nicola Hawe, Rick de Waard, Cynthia Leung, Mahyar Nouri-Shirazi, Attilio Orazi, R.S.K. Chaganti, Paul Rothman, Alan M. Stall, Pier-Paolo Pandolfi
& Riccardo Dalla-Favera doi:10.1038/ng0697-161 Abstract + references|PDF
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An imprinting element from the mouse H19 locus functions as a silencer in Drosophilapp171 - 173 Frank Lyko, James D. Brenton, M. Azim Surani
& Renato Paro doi:10.1038/ng0697-171 Abstract + references|PDF
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SOX9 directly regulates the type-ll collagen genepp174 - 178 Donald M. Bell, Keith K.H. Leung, Susan C. Wheatley, Ling Jim Ng, Sheila Zhou, Kam Wing Ling, Mai Har Sham, Peter Koopman, Patrick P.L. Tam
& Kathryn S.E. Cheah doi:10.1038/ng0697-174 Abstract + references|PDF
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PKD1 interacts with PKD2 through a probable coiled-coil domainpp179 - 183 Feng Qian, F. Joseph Germino, Yiqiang Cai, Xiangbin Zhang, Stefan Somlo
& Gregory G. Germino doi:10.1038/ng0697-179 Abstract + references|PDF
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Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophypp184 - 187 Alan D. Irvine, Laura D. Corden, Ole Swensson, Beate Swensson, Jonathan E. Moore, David G. Frazer, Frances J.D. Smith, Robert G. Knowlton, Enno Christophers, Rainer Rochels, Jouni Uitto
& W.H. Irwin McLean doi:10.1038/ng0697-184 Abstract + references|PDF
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Mutations in the myosin VIIA gene cause non-syndromic recessive deafnesspp188 - 190 Xue-Zhong Liu, James Walsh, Philomena Mburu, John Kendrick-Jones, M. Jamie T.V. Cope, Karen P. Steel
& Steve D.M. Brown doi:10.1038/ng0697-188 Abstract + references|PDF
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The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA genepp191 - 193 Dominique Weil, Polonca Küssel, Stéphane Blanchard, Gallia Lévy, Fabienne Levi-Acobas, Mohamed Drira, Hammadi Ayadi
& Christine Petit doi:10.1038/ng0697-191 Abstract + references|PDF
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Localization of genes controlling resistance to trypanosomiasis in micepp194 - 196 Stephen J. Kemp, Fuad Iraqi, Ariel Darvasi, Morris Soller
& Alan J. Teale doi:10.1038/ng0697-194 Abstract + references|PDF
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Quantitative trait loci for cellular defects in glucose and fatty acid metabolism in hypertensive ratspp197 - 201 Timothy J. Aitman, Takanari Gotoda, Alison L. Evans, Helen Imrie, Karen E. Heath, Paul M. Trembling, Hazel Truman, Caroline A. Wallace, Ahmadur Rahman, Caroline Doré, Jonathan Flint, Vladimir Kren, Vaclav Zidek, Theodore W. Kurtz, Michal Pravenec
& James Scott doi:10.1038/ng0697-197 Abstract + references|PDF
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Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21pp202 - 205 Traci A. Mansfield, David B. Simon, Zvi Farfel, Margaret Bia, Joseph R. Tucci, Marcel Lebe, Michael Gutkin, Bernard Vialettes, Marie A. Christofilis, Ritva Kauppinen-Makelin, Haim Mayan, Neil Risch
& Richard P. Lifton doi:10.1038/ng0697-202 Abstract + references|PDF
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