Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancerpp331 - 334 Felix Mitelman, Bertil Johansson
& Fredrik Mertens Published online: 30 March 2004|doi:10.1038/ng1335 Abstract|Full text|PDF
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Limited number of patrilines in horse domesticationpp335 - 336 Gabriella Lindgren, Niclas Backström, June Swinburne, Linda Hellborg, Annika Einarsson, Kaj Sandberg, Gus Cothran, Carles Vilà, Matthew Binns
& Hans Ellegren Published online: 14 March 2004|doi:10.1038/ng1326 Abstract|Full text|PDF
(105K)
|Supplementary Information
A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetespp337 - 338 Nunzio Bottini, Lucia Musumeci, Andres Alonso, Souad Rahmouni, Konstantina Nika, Masoud Rostamkhani, James MacMurray, Gian Franco Meloni, Paola Lucarelli, Maurizio Pellecchia, George S Eisenbarth, David Comings
& Tomas Mustelin Published online: 07 March 2004|doi:10.1038/ng1323 Abstract|Full text|PDF
(185K)
|Supplementary Information
A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndromepp339 - 341 Gevork N Mnatzakanian, Hannes Lohi, Iulia Munteanu, Simon E Alfred, Takahiro Yamada, Patrick J M MacLeod, Julie R Jones, Stephen W Scherer, N Carolyn Schanen, Michael J Friez, John B Vincent
& Berge A Minassian Published online: 21 March 2004|doi:10.1038/ng1327 Abstract|Full text|PDF
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|Supplementary Information
Inactivation of the Wip1 phosphatase inhibits mammary tumorigenesis through p38 MAPK−mediated activation of the p16Ink4a-p19Arf pathwaypp343 - 350 Dmitry V Bulavin, Crissy Phillips, Bonnie Nannenga, Oleg Timofeev, Larry A Donehower, Carl W Anderson, Ettore Appella
& Albert J Fornace Jr. Published online: 29 February 2004|doi:10.1038/ng1317 Abstract|Full text|PDF
(1,471K)
|Supplementary Information See also:News and Views by Bernards
Rb regulates proliferation and rod photoreceptor development in the mouse retinapp351 - 360 Jiakun Zhang, Jonathan Gray, Lizhao Wu, Gustavo Leone, Sheldon Rowan, Constance L Cepko, Xuemei Zhu, Cheryl M Craft
& Michael A Dyer Published online: 29 February 2004|doi:10.1038/ng1318 Abstract|Full text|PDF
(2,557K)
|Supplementary Information
Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutationspp361 - 369 Ken Inoue, Mehrdad Khajavi, Tomoko Ohyama, Shin-ichi Hirabayashi, John Wilson, James D Reggin, Pedro Mancias, Ian J Butler, Miles F Wilkinson, Michael Wegner
& James R Lupski Published online: 07 March 2004|doi:10.1038/ng1322 Abstract|Full text|PDF
(889K)
|Supplementary Information
Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1)pp371 - 376 Päivi Pajukanta, Heidi E Lilja, Janet S Sinsheimer, Rita M Cantor, Aldons J Lusis, Massimiliano Gentile, Xiaoqun Joyce Duan, Aino Soro-Paavonen, Jussi Naukkarinen, Janna Saarela, Markku Laakso, Christian Ehnholm, Marja-Riitta Taskinen
& Leena Peltonen Published online: 29 February 2004|doi:10.1038/ng1320 Abstract|Full text|PDF
(145K)
|Supplementary Information See also:News and Views by Shoulders
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing proteinpp377 - 381 Giles D J Watts, Jill Wymer, Margaret J Kovach, Sarju G Mehta, Steven Mumm, Daniel Darvish, Alan Pestronk, Michael P Whyte
& Virginia E Kimonis Published online: 21 March 2004|doi:10.1038/ng1332 Abstract|Full text|PDF
(706K)
|Supplementary Information
ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gatingpp382 - 387 Martin Bienengraeber, Timothy M Olson, Vitaliy A Selivanov, Eva C Kathmann, Fearghas O'Cochlain, Fan Gao, Amy B Karger, Jeffrey D Ballew, Denice M Hodgson, Leonid V Zingman, Yuan-Ping Pang, Alexey E Alekseev
& Andre Terzic Published online: 21 March 2004|doi:10.1038/ng1329 Abstract|Full text|PDF
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Assessing the impact of population stratification on genetic association studiespp388 - 393 Matthew L Freedman, David Reich, Kathryn L Penney, Gavin J McDonald, Andre A Mignault, Nick Patterson, Stacey B Gabriel, Eric J Topol, Jordan W Smoller, Carlos N Pato, Michele T Pato, Tracey L Petryshen, Laurence N Kolonel, Eric S Lander, Pamela Sklar, Brian Henderson, Joel N Hirschhorn
& David Altshuler Published online: 28 March 2004|doi:10.1038/ng1333 Abstract|Full text|PDF
(161K)
|Supplementary Information
Allele-specific repression of lymphotoxin- by activated B cell factor-1pp394 - 399 Julian C Knight, Brendan J Keating
& Dominic P Kwiatkowski Published online: 28 March 2004|doi:10.1038/ng1331 Abstract|Full text|PDF
(1,751K)
|Supplementary Information
Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis−renal dysfunction−cholestasis (ARC) syndromepp400 - 404 Paul Gissen, Colin A Johnson, Neil V Morgan, Janneke M Stapelbroek, Tim Forshew, Wendy N Cooper, Patrick J McKiernan, Leo W J Klomp, Andrew A M Morris, James E Wraith, Patricia McClean, Sally A Lynch, Richard J Thompson, Bryan Lo, Oliver W Quarrell, Maja Di Rocco, Richard C Trembath, Hanna Mandel, S Wali, Fiona E Karet, A S Knisely, Roderick H J Houwen, Deirdre A Kelly
& Eamonn R Maher Published online: 28 March 2004|doi:10.1038/ng1325 Abstract|Full text|PDF
(1,288K)
|Supplementary Information
Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesispp405 - 410 Deborah Krakow, Stephen P Robertson, Lily M King, Timothy Morgan, Eiman T Sebald, Cristina Bertolotto, Sebastian Wachsmann-Hogiu, Dora Acuna, Sandor S Shapiro, Toshiro Takafuta, Salim Aftimos, Chong Ae Kim, Helen Firth, Carlos E Steiner, Valerie Cormier-Daire, Andrea Superti-Furga, Luisa Bonafe, John M Graham Jr, Arthur Grix, Carlos A Bacino, Judith Allanson, Martin G Bialer, Ralph S Lachman, David L Rimoin
& Daniel H Cohn Published online: 29 February 2004|doi:10.1038/ng1319 Abstract|Full text|PDF
(1,376K)
|Supplementary Information See also:News and Views by Biesecker
Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCORpp411 - 416 David Ng, Nalin Thakker, Connie M Corcoran, Dian Donnai, Rahat Perveen, Adele Schneider, Donald W Hadley, Cynthia Tifft, Liqun Zhang, Andrew O M Wilkie, Jasper J van der Smagt, Robert J Gorlin, Shawn M Burgess, Vivian J Bardwell, Graeme C M Black
& Leslie G Biesecker Published online: 07 March 2004|doi:10.1038/ng1321 Abstract|Full text|PDF
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Epigenetic inactivation of SFRP genes allows constitutive WNT signaling in colorectal cancerpp417 - 422 Hiromu Suzuki, D Neil Watkins, Kam-Wing Jair, Kornel E Schuebel, Sanford D Markowitz, Wei Dong Chen, Theresa P Pretlow, Bin Yang, Yoshimitsu Akiyama, Manon van Engeland, Minoru Toyota, Takashi Tokino, Yuji Hinoda, Kohzoh Imai, James G Herman
& Stephen B Baylin Published online: 14 March 2004|doi:10.1038/ng1330 Abstract|Full text|PDF
(1,755K)
|Supplementary Information
Pervasive joint influence of epistasis and plasticity on mutational effects in Escherichia colipp423 - 426 Susanna K Remold
& Richard E Lenski Published online: 14 March 2004|doi:10.1038/ng1324 Abstract|Full text|PDF
(118K)
|Supplementary Information
Erratum: Intense and highly localized gene conversion activity in human meiotic crossover hot spotsp427 A J Jeffreys
& C A May doi:10.1038/ng0404-427a Full text|PDF
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Corrigendum: Gene expression−based high-throughput screening (GE-HTS) and application to leukemia differentiationp427 K Stegmaier, K N Ross, S A Colavito, S O'Malley, B R Stockwell
& T R Golub doi:10.1038/ng0404-427b Full text|PDF
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Corrigendum: The hyh mutation uncovers roles for Snap in apical protein localization and control of neural cell fatep427 T H Chae, S Kim, K E Marz, P I Hanson
& C A Walsh doi:10.1038/ng0404-427c Full text|PDF
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by activated B cell factor-1
