A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardationpp13 - 14 Karine Merienne, Sylvie Jacquot, Solange Pannetier, Maria Zeniou, Agnes Bankier, Jozef Gecz, Jean-Louis Mandel, John Mulley, Paolo Sassone-Corsi
& André Hanauer doi:10.1038/8719 Full text|PDF
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Necdin-deficient mice do not show lethality or the obesity and infertility
of Prader-Willi syndromepp15 - 16 Ting-Fen Tsai, Dawna Armstrong
& Arthur L. Beaudet doi:10.1038/8722 Full text|PDF
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-2 macroglobulin polymorphism and Alzheimer disease risk in the UKpp16 - 17 David J. Dow, Nicola Lindsey, Nigel J. Cairns, Carol Brayne, Damian Robinson, Felicia A. Huppert, Eugene S. Paykel, John Xuereb, Gordon Wilcock, Joanne L. Whittaker
& David C. Rubinsztein doi:10.1038/8724 Full text|PDF
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-2 macroglobulin gene and Alzheimer diseasepp17 - 19 Varuni Rudrasingham, Fabienne Wavrant-De Vrièze, Jean-Charles Lambert, Sumi Chakraverty, Patrick Kehoe, Richard Crook, Philippe Amouyel, William Wu, Frances Rice, Jordi Pérez-Tur, Bernard Frigard, John C. Morris, Stephanie Carty, Ronald Petersen, Dominique Cottel, Nigel Tunstall, Peter Holmans, Simon Lovestone, Marie-Christine Chartier-Harlin, Alison Goate, John Hardy, Michael J. Owen
& Julie Williams doi:10.1038/8726 Full text|PDF
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An -2-macroglobulin insertion-deletion polymorphism in Alzheimer
diseasepp19 - 21 Ekaterina A. Rogaeva, Smita Premkumar, Janet Grubber, Lutgarde Serneels, William K. Scott, Toshitaka Kawarai, Youqiang Song, De'Lisa M. Hill, Suzanne M. Abou-Donia, Eden R. Martin, Jeffrey J. Vance, Gang Yu, Antonio Orlacchio, York Pei, Masaki Nishimura, Agres Supala, Brenda Roberge, Ann M. Saunders, Allen D. Roses, Donald Schmechel, Alison Crane-Gatherum, Sandro Sorbi, Amalia Bruni, Gary W. Small, P. Michael Conneally, Jonathan L. Haines, Fred Van Leuven, Peter H. St. George-Hyslop, Lindsay A. Farrer
& Margaret A. Pericak-Vance doi:10.1038/8729 Full text|PDF
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An -2-macroglobulin insertion-deletion polymorphism in Alzheimer
disease (reply)pp21 - 22 Deborah Blacker, Adam S. Crystal, Marsha A. Wilcox, Nan M. Laird
& Rudolph E. Tanzi doi:10.1038/8732 Full text|PDF
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Distribution and early development of microarray technology in Europep22 Andreas Vente, Bernd Korn, Günther Zehetner, Annemarie Poustka
& Hans Lehrach doi:10.1038/8734 Full text|PDF
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Status, sale and patenting of human genetic material: an international
surveypp23 - 26 Bartha Maria Knoppers doi:10.1038/8735 Abstract|Full text|PDF
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A radiation hybrid map of the rat genome containing 5,255 markerspp27 - 36 Takeshi K. Watanabe, Marie-Therese Bihoreau, Linda C. McCarthy, Susanna L. Kiguwa, Haretsugu Hishigaki, Atsushi Tsuji, Julie Browne, Yuki Yamasaki, Ayako Mizoguchi-Miyakita, Keiko Oga, Toshihide Ono, Shiro Okuno, Naohide Kanemoto, Ei-ichi Takahashi, Kazuhiro Tomita, Hiromi Hayashi, Masakazu Adachi, Caleb Webber, Marie Davis, Susanne Kiel, Catherine Knights, Angela Smith, Ricky Critcher, Jonathan Miller, Thiru Thangarajah, Philip J.R. Day, James R. Hudson Jr, Yasuo Irie, Toshihisa Takagi, Yusuke Nakamura, Peter N. Goodfellow, G. Mark Lathrop, Akira Tanigami
& Michael R. James doi:10.1038/8737 Abstract|Full text|PDF
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Conditional mutation of Brca1 in mammary epithelial cells results
in blunted ductal morphogenesis and tumour formationpp37 - 43 Xiaoling Xu, Kay-Uwe Wagner, Denise Larson, Zoë Weaver, Cuiling Li, Thomas Ried, Lothar Hennighausen, Anthony Wynshaw-Boris
& Chu-Xia Deng doi:10.1038/8743 Abstract|Full text|PDF
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Loss of Cdk4 expression causes insulin-deficient diabetes and Cdk4 activation results in -islet cell hyperplasiapp44 - 52 Sushil G. Rane, Pierre Dubus, Richard V. Mettus, Elizabeth J. Galbreath, Guenther Boden, E. Premkumar Reddy
& Mariano Barbacid doi:10.1038/8751 Abstract|Full text|PDF
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Action of BTN1, the yeast orthologue of the gene mutated in Batten
diseasepp55 - 58 David A. Pearce, Tracy Ferea, Seth A. Nosel, Biswadip Das
& Fred Sherman doi:10.1038/8861 Abstract|Full text|PDF
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Sequence variation in the human angiotensin converting enzymepp59 - 62 Mark J. Rieder, Scott L. Taylor, Andrew G. Clark
& Deborah A. Nickerson doi:10.1038/8760 Abstract|Full text|PDF
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Inactivating mutations and overexpression of BCL10, a caspase
recruitment domain-containing gene, in MALT lymphoma with t(1;14)(p22;q32)
pp63 - 68 Quangeng Zhang, Reiner Siebert, Minhong Yan, Bernd Hinzmann, Xiaoli Cui, Liquan Xue, Karen M. Rakestraw, Clayton W. Naeve, Georg Beckmann, Dennis D. Weisenburger, Warren G. Sanger, Hadwiga Nowotny, Michael Vesely, Evelyne Callet-Bauchu, Gilles Salles, Vishva M. Dixit, André Rosenthal, Brigitte Schlegelberger
& Stephan W. Morris doi:10.1038/8767 Abstract|Full text|PDF
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Epidermal growth factor receptor function is necessary for normal craniofacial
development and palate closurepp69 - 73 Päivi J. Miettinen, Jennie R. Chin, Lillian Shum, Harold C. Slavkin, Charles F. Shuler, Rik Derynck
& Zena Werb doi:10.1038/8773 Abstract|Full text|PDF
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Alymphoplasia is caused by a point mutation in the mouse gene encoding
Nf-b-inducing kinasepp74 - 77 Reiko Shinkura, Kazuhiro Kitada, Fumihiko Matsuda, Kei Tashiro, Koichi Ikuta, Misao Suzuki, Katsumi Kogishi, Tadao Serikawa
& Tasuku Honjo doi:10.1038/8780 Abstract|Full text|PDF
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DNA sequence variation in a non-coding region of low recombination on
the human X chromosomepp78 - 81 Henrik Kaessmann, Florian Heiig, Arndt von Haeseler
& Svante Pääbo doi:10.1038/8785 Abstract|Full text|PDF
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Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson
syndromepp82 - 84 Saori Kitao, Akira Shimamoto, Makoto Goto, Robert W. Miller, William A. Smithson, Noralane M. Lindor
& Yasuhiro Furuichi doi:10.1038/8788 Abstract|Full text|PDF
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Sox9 is required for cartilage formationpp85 - 89 Weimin Bi, Jian Min Deng, Zhaoping Zhang, Richard R. Behringer
& Benoit de Crombrugghe doi:10.1038/8792 Abstract|Full text|PDF
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Position of a 'green-red' hybrid gene in the visual pigment array determines
colour-vision phenotypepp90 - 93 Takaaki Hayashi, Arno G. Motulsky
& Samir S. Deeb doi:10.1038/8798 Abstract|Full text|PDF
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Acetylated histones are associated with FMR1 in normal but not
fragile X-syndrome cellspp98 - 101 Bradford Coffee, Fuping Zhang, Stephen T. Warren
& Daniel Reines doi:10.1038/8807 Abstract|Full text|PDF
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c-MYC interacts with INI1/hSNF5 and requires the SWI/SNF complex for
transactivation functionpp102 - 105 S.-W. Grace Cheng, Kelvin P. Davies, Eric Yung, Ralph J. Beltran, Jin Yu
& Ganjam V. Kalpana doi:10.1038/8811 Abstract|Full text|PDF
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Evolution of neoplastic cell lineages in Barrett oesophaguspp106 - 109 Michael T. Barrett, Carissa A. Sanchez, Laura J. Prevo, David J. Wong, Patricia C. Galipeau, Thomas G. Paulson, Peter S. Rabinovitch
& Brian J. Reid doi:10.1038/8816 Abstract|Full text|PDF
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Synphilin-1 associates with -synuclein and promotes the formation of cytosolic inclusionspp110 - 114 Simone Engelender, Zachary Kaminsky, Xin Guo, Alan H. Sharp, Ravi K. Amaravi, John J. Kleiderlein, Russell L. Margolis, Juan C. Troncoso, Anthony A. Lanahan, Paul F. Worley, Valina L. Dawson, Ted M. Dawson
& Christopher A. Ross doi:10.1038/8820 Abstract|Full text|PDF
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-2 macroglobulin polymorphism and Alzheimer disease risk in the UK
-islet cell hyperplasia
b-inducing kinase
ig, Arndt von Haeseler
& Svante Pääbo
