Research in Indiap142 Vishwajit L. Nimgaonkar doi:10.1038/ng0696-142a PDF
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CNTF and psychiatric disorderspp142 - 144 Markus M. Nöthen, Sven Cichon, Katja Eggermann, Peter Propping, Michael Knapp, Wolfgang Maier
& Marcella Rietschel doi:10.1038/ng0696-142b References|PDF
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CNTF and psychiatric disorderspp143 - 144 Tao Li, Homero Vallada, Rachel Bell, Xiehe Liu, Tao Xie
& David A. Collier doi:10.1038/ng0696-143 References|PDF
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Reply to "CNTF and psychiatric disorders"p144 Johannes Thome, Michael Rösier, Peter Riederer
& Johannes Kornhuber doi:10.1038/ng0696-144a References|PDF
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Biotinidase mutational 'hotspot'pp144 - 145 Alasdair Gordon doi:10.1038/ng0696-144b References|PDF
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Identification of sex−specific quantitative trait loci controlling alcohol preference in C57BL/6 micepp147 - 153 Justine A. Melo, Jay Shendure, Kara Pociask
& Lee M. Silver doi:10.1038/ng0696-147 Abstract + references|PDF
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Minisatellite diversity supports a recent African origin for modern humanspp154 - 160 John A.L. Armour, Tiiu Anttinen, Celia A. May, Emilce E. Vega, Antti Sajantila, Judith R. Kidd, Kenneth K. Kidd, Jaume Bertranpetit, Svante Pääbo
& Alec J. Jeffreys doi:10.1038/ng0696-154 Abstract + references|PDF
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A genome−wide search for human non−insulin−dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2pp161 - 166 C.L. Hanis, E. Boerwinkle, R. Chakraborty, D.L. Ellsworth, P. Concannon, B. Stirling, V.A. Morrison, B. Wapelhorst, R.S. Spielman, K.J. Gogolin-Ewens, J.M. Shephard, S.R. Williams, N. Risch, D. Hinds, N. Iwasaki, M. Ogata, Y. Omori, C. Petzold, H. Rietzsch, H.-E. Schröder, J. Schulze, N.J. Cox, S. Menzel, V.V. Boriraj, X. Chen, L.R. Lim, T. Lindner, L.E. Mereu, Y.-Q. Wang, K. Xiang, K. Yamagata, Y. Yang
& G.I. Bell doi:10.1038/ng0696-161 Abstract + references|PDF
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Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searchingpp167 - 174 Sandro Banfi, Giuseppe Borsani, Elena Rossi, Loris Bernard, Alessandro Guffanti, Francesca Rubboli, Anna Marchitiello, Sabrina Giglio, Elisabetta Coluccia, Massimo Zollo, Orsetta Zuffardi
& Andrea Ballabio doi:10.1038/ng0696-167 Abstract + references|PDF
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A gene mutated in X−linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeastpp175 - 182 Jocelyn Laporte, Ling Jia Hu, Christine Kretz, Jean-Louis Mandel, Petra Kioschis, Johannes F. Coy, Sabine M. Klauck, Annemarie Poustka
& Niklas Dahl doi:10.1038/ng0696-175 Abstract + references|PDF
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Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na−K−2CI cotransporter NKCC2pp183 - 188 David B. Simon, Fiona E. Karet, Jahed M. Hamdan, Antonio Di Pietro, Sami A. Sanjad
& Richard P. Lifton doi:10.1038/ng0696-183 Abstract + references|PDF
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Mutations in the activin receptor−like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2pp189 - 195 D.W. Johnson, J.N. Berg, M.A. Baldwin, C.J. Gallione, I. Marondel, S.-J. Yoon, T.T. Stenzel, M. Speer, M.A. Pericak-Vance, A. Diamond, A.E. Guttmacher, C.E. Jackson, L. Attisano, R. Kucherlapati, M.E.M. Porteous
& D.A. Marchuk doi:10.1038/ng0696-189 Abstract + references|PDF
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Expanded polyglutamine in the Machado−Joseph disease protein induces cell death in vitro and in vivopp196 - 202 Hanako Ikeda, Masahiro Yamaguchi, Satoshi Sugai, Yoshiya Aze, Shuh Narumiya
& Akira Kakizuka doi:10.1038/ng0696-196 Abstract + references|PDF
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Glucose−6−phosphatase dependent substrate transport in the glycogen storage disease type−1a mousepp203 - 209 Ke-Jian Lei, Hungwen Chen, Chi-Jiunn Pan, Jerrold M. Ward, Bedrich Mosinger Jr. Jr., Eric J. Lee, Heiner Westphal, Brian C. Mansfield
& Janice Yang Chou doi:10.1038/ng0696-203 Abstract + references|PDF
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A functionally defective allele of TAP1 results in loss of MHC class I antigen presentation in a human lung cancerpp210 - 213 Hailei L. Chen, Dmitry Gabrilovich, Robert Tampé, Khaled R. Girgis, Sorena Nadaf
& David P. Carbone doi:10.1038/ng0696-210 Abstract + references|PDF
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Ankyrin−1 mutations are a major cause of dominant and recessive hereditary spherocytosispp214 - 218 Stefan W. Eber, Jennifer M. Gonzalez, Marcia L. Lux, Alphonse L. Scarpa, William T. Tse, Marion Dornwell, Jutta Herbers, Wilfried Kugler, Refik Ozcan, Arnulf Pekrun, Patrick G. Gallagher, Werner Schroter, Bernard G. Forget
& Samuel E. Lux doi:10.1038/ng0696-214 Abstract + references|PDF
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A murine model of Menkes disease reveals a physiological function of metallothioneinpp219 - 222 Edward J. Kelly
& Richard D. Palmiter doi:10.1038/ng0696-219 Abstract + references|PDF
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Characterization of DRP2, a novel human dystrophin homologuepp223 - 226 Roland G. Roberts, Tom C. Freeman, Elaine Kendall, David L.P. Vetrie, Alistair K. Dixon, Charles Shaw-Smith, Quentin Bone
& Martin Bobrow doi:10.1038/ng0696-223 Abstract + references|PDF
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A synaptobrevin−like gene in the Xq28 pseudoautosomal region undergoes X inactivationpp227 - 229 Maurizio D'Esposito, Alfredo Ciccodicola, Fernando Gianfrancesco, Teresa Esposito, Luisa Flagiello, Richard Mazzarella, David Schlessinger
& Michele D'Urso doi:10.1038/ng0696-227 Abstract + references|PDF
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Sex reversal by loss of the C−terminal transactivation domain of human SOX9pp230 - 232 Peter Südbeck, M. Lienhard Schmitz, Patrick A. Baeuerle
& Gerd Scherer doi:10.1038/ng0696-230 Abstract + references|PDF
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Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasiapp233 - 237 Michael C. Naski, Qing Wang, Jingsong Xu
& David M. Ornitz doi:10.1038/ng0696-233 Abstract + references|PDF
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BRCA2 mutations in primary breast and ovarian cancerspp238 - 240 Johnathan M. Lancaster, Richard Wooster, Jonathon Mangion, Catherine M. Phelan, Charles Cochran, Curtis Gumbs, Sheila Seal, Rita Barfoot, Nadine Collins, Graham Bignell, Sandeep Patel, Rifat Hamoudi, Catharina Larsson, Roger W. Wiseman, Andrew Berchuck, J. Dirk Iglehart, Jeffrey R. Marks, Alan Ashworth, Michael R. Stratton
& P. Andrew Futreal doi:10.1038/ng0696-238 Abstract + references|PDF
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Low incidence of BRCA2 mutations in breast carcinoma and other cancerspp241 - 244 David H.-R Teng, Robert Bogden, Jeffrey Mitchell, Michelle Baumgard, Russell Bell, Simin Berry, Thaylon Davis, Phuong C. Ha, Robert Kehrer, Srikanth Jammulapati, Qian Chen, Kenneth Offit, Mark H. Skolnick, Sean V. Tavtigian, Suresh Jhanwar, Brad Swedlund, Alexander K.C. Wong
& Alexander Kamb doi:10.1038/ng0696-241 Abstract + references|PDF
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Mutation analysis in the BRCA2 gene in primary breast cancerspp245 - 247 Yoshio Miki, Toyomasa Katagiri, Fujio Kasumi, Takamasa Yoshimoto
& Yusuke Nakamura doi:10.1038/ng0696-245 Abstract + references|PDF
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A novel spice−site mutation in the subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 familiespp248 - 250 Sandra S. Strautnieks, Richard J. Thompson, R. Mark Gardiner
& Eddie Chung doi:10.1038/ng0696-248 Abstract + references|PDF
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subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 families
