Incorrect use of the term syntenyp387 Eberhard Passarge, Bernhard Horsthemke
& Rosann A Farber doi:10.1038/70486 Full text|PDF
(75K)
Analysis of human transcriptomespp387 - 388 Victor E Velculescu, Stephen L Madden, Lin Zhang, Alex E Lash, Jian Yu, Carlo Rago, Anita Lal, Clarence J Wang, Gary A Beaudry, Kristin M Ciriello, Brian P Cook, Michael R Dufault, Anne T Ferguson, Yuhong Gao, Tong-Chuan He, Heiko Hermeking, Siewleng K Hiraldo, Paul M Hwang, Marissa A Lopez, Hilary F Luderer, Brynna Mathews, Joseph M Petroziello, Kornelia Polyak, Leigh Zawel, Wen Zhang, Xiaoming Zhang, Wei Zhou, Frank G Haluska, Jin Jen, Saraswati Sukumar, Gregory M Landes, Gregory J Riggins, Bert Vogelstein
& Kenneth W Kinzler doi:10.1038/70487 Full text|PDF
(89K)
|Supplementary Information
Vestiges of a DNA methylation system in Drosophila melanogaster?pp389 - 390 Susan Tweedie, Huck-Hui Ng, Andrew L. Barlow, Bryan M. Turner, Brian Hendrich
& Adrian Bird doi:10.1038/70490 Abstract|Full text|PDF
(364K)
Expansion of a novel CAG trinucleotide repeat in the 5' region
of PPP2R2B is associated with SCA12pp391 - 392 Susan E Holmes, Elizabeth E O'Hearn, Melvin G McInnis, Daniel A Gorelick-Feldman, John J Kleiderlein, Colleen Callahan, Noeun G Kwak, Roxann G Ingersoll-Ashworth, Meeia Sherr, August J Sumner, Alan H Sharp, Uma Ananth, William K Seltzer, Michael A Boss, Ana-Maria Vieria-Saecker, Jörg T Epplen, Olaf Riess, Christopher A Ross
& Russell L Margolis doi:10.1038/70493 Abstract|Full text|PDF
(282K)
|Supplementary Information
Mutations in RGR, encoding a light-sensitive opsin homologue,
in patients with retinitis pigmentosapp393 - 394 Hiroyuki Morimura, Florence Saindelle-Ribeaudeau, Eliot L Berson
& Thaddeus P Dryja doi:10.1038/70496 Abstract|Full text|PDF
(291K)
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)
pp413 - 419 Wyman T. McGuirt, Sai D. Prasad, Andrew J. Griffith, Henricus P.M. Kunst, Glenn E. Green, Karl B. Shpargel, Christina Runge, Christy Huybrechts, Robert F. Mueller, Eric Lynch, Mary-Claire King, Han G. Brunner, Cor W.R.J. Cremers, Masamine Takanosu, Shi-Wu Li, Machiko Arita, Richard Mayne, Darwin J. Prockop, Guy Van Camp
& Richard J.H. Smith doi:10.1038/70516 Abstract|Full text|PDF
(1,234K)
Loss-of-function mutations in the cathepsin C gene result in periodontal
disease and palmoplantar keratosispp421 - 424 Carmel Toomes, Jacqueline James, A. Joseph Wood, Chu Lee Wu, Derek McCormick, Nicholas Lench, Chelsee Hewitt, Leanne Moynihan, Emma Roberts, C. Geoffrey Woods, Alexander Markham, Melanie Wong, Richard Widmer, Khaled Abdul Ghaffar, Michael Pemberton, Ibtessam Ramzy Hussein, Samia A. Temtamy, Robin Davies, Andrew P. Read, Philip Sloan, Michael J. Dixon
& Nalin S. Thakker doi:10.1038/70525 Abstract|Full text|PDF
(474K)
See also:News and Views by Nuckolls & Slavkin
Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70pp425 - 428 John M. Warrick, H.Y. Edwin Chan, Gladys L. Gray-Board, Yaohui Chai, Henry L. Paulson
& Nancy M. Bonini doi:10.1038/70532 Abstract|Full text|PDF
(1,228K)
An azoospermic man with a de novo point mutation in the Y-chromosomal
gene USP9Ypp429 - 432 Chao Sun, Helen Skaletsky, Bruce Birren, Keri Devon, Zhaolan Tang, Sherman Silber, Robert Oates
& David C. Page doi:10.1038/70539 Abstract|Full text|PDF
(364K)
Mutations in ELA2, encoding neutrophil elastase, define a 21-day
biological clock in cyclic haematopoiesispp433 - 436 Marshall Horwitz, Kathleen F. Benson, Richard E. Person, Andrew G. Aprikyan
& David C. Dale doi:10.1038/70544 Abstract|Full text|PDF
(290K)
Genetic evidence of an early exit of Homo sapiens sapiens from Africa through eastern Africapp437 - 441 Lluís Quintana-Murci, Ornella Semino, Hans-J. Bandelt, Giuseppe Passarino, Ken McElreavey
& A. Silvana Santachiara-Benerecetti doi:10.1038/70550 Abstract|Full text|PDF
(185K)
Atp6i-deficient mice exhibit severe osteopetrosis due to loss of osteoclast-mediated extracellular acidificationpp447 - 451 Yi-Ping Li, Wei Chen, Yuqiong Liang, En Li
& Philip Stashenko doi:10.1038/70563 Abstract|Full text|PDF
(1,234K)
A general approach to single-nucleotide polymorphism discoverypp452 - 456 Gabor T. Marth, Ian Korf, Mark D. Yandell, Raymond T. Yeh, Zhijie Gu, Hamideh Zakeri, Nathan O. Stitziel, LaDeana Hillier, Pui-Yan Kwok
& Warren R. Gish doi:10.1038/70570 Abstract|Full text|PDF
(125K)
Heterochromatin protein 1 modifies mammalian PEV in a dose- and chromosomal-context- dependent
mannerpp457 - 461 Richard Festenstein, Soheila Sharghi-Namini, Margaret Fox, Kathleen Roderick, Mauro Tolaini, Trisha Norton, Alexander Saveliev, Dimitris Kioussis
& Prim Singh doi:10.1038/70579 Abstract|Full text|PDF
(317K)
A new gene, encoding an anion transporter, is mutated in sialic acid storage diseasespp462 - 465 Frans W. Verheijen, Elly Verbeek, Nina Aula, Cecile E.M.T. Beerens, Adrie C. Havelaar, Marijke Joosse, Leena Peltonen, Pertti Aula, Hans Galjaard, Peter J. van der Spek
& Grazia M.S. Mancini doi:10.1038/70585 Abstract|Full text|PDF
(1,463K)
Retinopathy and attenuated circadian entrainment in Crx-deficient
micepp466 - 470 Takahisa Furukawa, Eric M. Morrow, Tiansen Li, Fred C. Davis
& Constance L. Cepko doi:10.1038/70591 Abstract|Full text|PDF
(958K)
Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic micepp471 - 473 Kevin Manley, Thomas L. Shirley, Lorraine Flaherty
& Anne Messer doi:10.1038/70598 Abstract|Full text|PDF
(119K)
Transcriptional repression mediated by the human polycomb-group protein
EED involves histone deacetylationpp474 - 478 Johan van der Vlag
& Arie P. Otte doi:10.1038/70602 Abstract|Full text|PDF
(210K)
Repression of the gene encoding the TGF- type II receptor is a major target of the EWS-FLI1 oncoproteinp481 Ki-Baik Hahm doi:10.1038/70611 Full text|PDF
(37K)
Delayed early embryonic lethality following disruption of the murine cyclin A2 genep481 Martin Murphy doi:10.1038/70612 Full text|PDF
(37K)
type II receptor is a major target of the EWS-FLI1 oncoprotein
Volumes 21 − 23
