Frataxin fracaspp337 - 338 Mireille Cossée, Victoria Campuzano, Hana Koutnikova, Kurt Fischbeck, Jean-Louis Mandel, Michel Koenig, Sanjay I. Bidichandani, Pragna I. Patel, Maria Dolores Moltè, Joaquin Cañizares, Rosa De Frutos, Luigi Pianese, Francesca Cavalcanti, Antonella Monticelli, Sergio Cocozza, Laura Montermini
& Massimo Pandolfo doi:10.1038/ng0497-337 References|PDF
(280K)
Reply to "Frataxin fracas"p338 Susan Chamberlain, Mark Pook, Jaime Carvajal, Kitm Doudney
& Renate Hillermann doi:10.1038/ng0497-338 References|PDF
(146K)
Genome cross-referencing and XREFdb: Implications for the identification and analysis of genes mutated in human diseasepp339 - 344 Douglas E. Bassett Jr., Mark S. Boguski, Forrest Spencer, Roger Reeves, Su-hyon Kim, Theresa Weaver
& Philip Hieter doi:10.1038/ng0497-339 Abstract + references|PDF
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Formation of de novo centromeres and construction of first-generation human artificial microchromosomespp345 - 355 John J. Harrington, Gil Van Bokkelen, Robert W. Mays, Karen Gustashaw
& Huntington F. Willard doi:10.1038/ng0497-345 Abstract + references|PDF
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Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancerspp356 - 362 Peter A. Steck, Mark A. Pershouse, Samar A. Jasser, W.K. Alfred Yung, Huai Lin, Azra H. Ligon, Lauren A. Langford, Michelle L. Baumgard, Thomas Hattier, Thaylon Davis, Cheryl Frye, Rong Hu, Bradley Swedlund, David H.R. Teng
& Sean V. Tavtigian doi:10.1038/ng0497-356 Abstract + references|PDF
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A high observed substitution rate in the human mitochondrial DNA control regionpp363 - 368 Thomas J. Parsons, David S. Muniec, Kevin Sullivan, Nicola Woodyatt, Rosemary Alliston-Greiner, Mark R. Wilson, Dianna L. Berry, Koren A. Holland, Victor W. Weedn, Peter Gill
& Mitchell M. Holland doi:10.1038/ng0497-363 Abstract + references|PDF
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Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctatapp369 - 376 Nancy Braverman, Gary Steel, Cassandra Obie, Ann Moser, Hugo Moser, Stephen J. Gould
& David Valle doi:10.1038/ng0497-369 Abstract + references|PDF
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Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptorpp377 - 380 Alison M. Motley, Ewald H. Hettema, Eveline M. Hogenhout, Pedro Brites, Anneloor L.M.A. ten Asbroek, Frits A. Wijburg, Frank Baas, Hugo S. Heijmans, Henk F. Tabak, Ronald J.A. Wanders
& Ben Distel doi:10.1038/ng0497-377 Abstract + references|PDF
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Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptorpp381 - 384 P. Edward Purdue, Jing Wei Zhang, Marek Skoneczny
& Paul B. Lazarow doi:10.1038/ng0497-381 Abstract + references|PDF
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Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorderspp385 - 388 Chia-Che Chang, Wen-Hui Lee, Hugo Moser, David Valle
& Stephen J. Gould doi:10.1038/ng0497-385 Abstract + references|PDF
(932K)
A genome-wide search for asthma susceptibility loci in ethnically diverse populations
pp389 - 392
Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1pp393 - 396 Kimmo Virtaneva, Elena D'Amato, Jinmin Miao, Marjaleena Koskiniemi, Reijo Norio, Giuliano Avanzini, Silvana Franceschetti, Roberto Michelucci, Carlo A. Tassinari, Salah Omer, Len A. Pennacchio, Richard M. Myers, José L. Dieguez-Lucena, Ralf Krahe, Albert de la Chapelle
& Anna-Elina Lehesjoki doi:10.1038/ng0497-393 Abstract + references|PDF
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Hypogonadism and obesity in mice with a targeted deletion of the Nhlh2 genepp397 - 401 Deborah J. Good, Forbes D. Porter, Kathleen A. Mahon, Albert F Parlow, Heiner Westphal
& Ilan R. Kirsch doi:10.1038/ng0497-397 Abstract + references|PDF
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Identification by DNA analysis of the victims of the August 1996 Spitsbergen civil aircraft disasterpp402 - 405 Bjørnar Olaisen, Margurethe Stenersen
& Bente Mevåg doi:10.1038/ng0497-402 Abstract + references|PDF
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Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotypingpp406 - 410 Tim Veldman, Christine Vignon, Evelin Schröck, Janet D. Rowley
& Thomas Ried doi:10.1038/ng0497-406 Abstract + references|PDF
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Erratum: A human candidate spermatogenesis gene, RBM1, is conserved and amplified on the marsupial Y chromosomep411 Margaret L. Delbridge, Jenny L. Harry, Roland Toder, Rachel J. Waugh O'Neill, Kun Ma, Ann C. Chandley
& Jennifer A. Marshall Graves doi:10.1038/ng0497-411a PDF
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Erratum: Promoter swapping between the genes for a novel zinc finger protein and -catenin in pleiomorphic adenomas with t(3;8)(p21;q12) translocationsp411 Koen Kas, Marianne L. Voz, Eva Röijer, Anna-Karin Åström, Eva Meyen, Göran Stenman
& Wim J.M. Van de Yen doi:10.1038/ng0497-411b PDF
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Erratum: Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndromep411 Craig T. Basson, David R. Bachinsky, Robert C. Lin, Tatjana Levi, Jacob A. Elkins, Johann Soults, David Grayzel, Elena Kroumpouzou, Thomas A. Traill, Janine Leblanc-Straceski, Beatrice Renault, Raju Kucherlapati, J.G. Seidman
& Christine E. Seidman doi:10.1038/ng0497-411c PDF
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Erratum:
UBE3A/E6-AP mutations cause Angelman syndromep411 T. Kishino, M. Lalande
& J. Wagstaff doi:10.1038/ng0497-411d PDF
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-catenin in pleiomorphic adenomas with t(3;8)(p21;q12) translocations
