Less from more: cosuppression of transposable elementspp148 - 149 James A Birchler, Manika Pal-Bhadra
& Utpal Bhadra doi:10.1038/5926 Full text|PDF
(131K)
See also:Letter by Jensen et al.
Extracellular matrix calcification: where is the action?pp150 - 151 Thorsten Schinke, Marc D McKee
& Gerard Karsenty doi:10.1038/5928 Full text|PDF
(96K)
Forever hopeful relations: chromatin, telomeres and checkpointspp151 - 152 Ted Weinert
& Victoria Lundblad doi:10.1038/5930 Full text|PDF
(80K)
See also:Letter by Corda et al.
An imprinted QTL with major effect on muscle mass and fat deposition
maps to the IGF2 locus in pigspp155 - 156 Carine Nezer, Laurence Moreau, Benoît Brouwers, Wouter Coppieters, Johann Detilleux, Roger Hanset, Latifa Karim, Alex Kvasz, Pascal Leroy
& Michel Georges doi:10.1038/5935 Full text|PDF
(264K)
A paternally expressed QTL affecting skeletal and cardiac muscle mass
in pigs maps to the IGF2 locuspp157 - 158 Jin-Tae Jeon, Örjan Carlborg, Anna Törnsten, Elisabetta Giuffra, Valerie Amarger, Patrick Chardon, Lena Andersson-Eklund, Kjell Andersson, Ingemar Hansson, Kerstin Lundström
& Leif Andersson doi:10.1038/5938 Full text|PDF
(128K)
QTL influencing autoimmune diabetes and encephalomyelitis map to a 0.15-cM
region containing Il2pp158 - 160 Jeffrey A. Encinas, Linda S. Wicker, Laurence B. Peterson, Akiko Mukasa, Cory Teuscher, Raymond Sobel, Howard L. Weiner, Christine E. Seidman, J.G. Seidman
& Vijay K. Kuchroo doi:10.1038/5941 Full text|PDF
(127K)
Late onset of renal and hepatic cysts in Pkd1-targeted heterozygotes
pp160 - 161 Weining Lu, Xiaohong Fan, Nuria Basora, Hermik Babakhanlou, Terry Law, Nader Rifai, Peter C. Harris, Antonio R. Perez-Atayde, Helmut G. Rennke
& Jing Zhou doi:10.1038/5944 Full text|PDF
(244K)
Human homologue of the Drosophila melanogaster lats tumour suppressor
modulates CDC2 activitypp177 - 181 Wufan Tao, Sheng Zhang, Gregory S Turenchalk, Rodney A Stewart, Maie A R St, Weili Chen
& Tian Xu doi:10.1038/5960 Abstract|Full text|PDF
(502K)
See also:News and Views by Kemp
Mice deficient of Lats1 develop soft-tissue sarcomas, ovarian
tumours and pituitary dysfunctionpp182 - 186 Maie A R St, Wufan Tao, Xiaolan Fei, Royd Fukumoto, Maria Luisa Carcangiu, David G Brownstein, Albert F Parlow, James McGrath
& Tian Xu doi:10.1038/5965 Abstract|Full text|PDF
(516K)
See also:News and Views by Kemp
Activating SRC mutation in a subset of advanced human colon cancers
pp187 - 190 Rosalyn B. Irby, Weiguang Mao, Domenico Coppola, Jimmy Kang, Jean Marc Loubeau, Walter Trudeau, Richard Karl, Donald J. Fujita, Richard Jove
& Timothy J. Yeatman doi:10.1038/5971 Abstract|Full text|PDF
(261K)
An encyclopedia of mouse genespp191 - 194 Marco Marra, LaDeana Hillier, Tamara Kucaba, Melissa Allen, Robert Barstead, Catherine Beck, Angela Blistain, Maria Bonaldo, Yvette Bowers, Louise Bowles, Marco Cardenas, Ann Chamberlain, Julie Chappell, Sandra Clifton, Anthony Favello, Steve Geisel, Marilyn Gibbons, Njata Harvey, Francesca Hill, Yolanda Jackson, Sophie Kohn, Greg Lennon, Elaine Mardis, John Martin, LeeAnne Mila, Rhonda McCann, Richard Morales, Deana Pape, Barry Person, Christa Prange, Erika Ritter, Marcelo Soares, Rebecca Schurk, Tanya Shin, Michele Steptoe, Timothy Swaller, Brenda Theising, Karen Underwood, Todd Wylie, Tamara Yount, Richard Wilson
& Robert Waterston doi:10.1038/5976 Abstract|Full text|PDF
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Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport,
is defective in the sla mousepp195 - 199 Christopher D. Vulpe, Yien-Ming Kuo, Therese L. Murphy, Lex Cowley, Candice Askwith, Natasha Libina, Jane Gitschier
& Gregory J. Anderson doi:10.1038/5979 Abstract|Full text|PDF
(504K)
Prolongation of ovarian lifespan into advanced chronological age by Bax-deficiencypp200 - 203 Gloria I. Perez, Rodolfo Robles, C. Michael Knudson, Jodi A. Flaws, Stanley J. Korsmeyer
& Jonathan L. Tilly doi:10.1038/5985 Abstract|Full text|PDF
(501K)
Interaction between Set1p and checkpoint protein Mec3p in DNA repair
and telomere functionspp204 - 208 Yves Corda, Vera Schramke, Maria Pia Longhese, Tamara Smokvina, Vera Paciotti, Vanessa Brevet, Eric Gilson
& Vincent Géli doi:10.1038/5991 Abstract|Full text|PDF
(686K)
See also:News and Views by Weinert & Lundblad
Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americanspp213 - 215 Nancy J. Cox, Mike Frigge, Dan L. Nicolae, Patrick Concannon, Craig L. Hanis, Graeme I. Bell
& Augustine Kong doi:10.1038/6002 Abstract|Full text|PDF
(94K)
Receptors for polytropic and xenotropic mouse leukaemia viruses encoded
by a single gene at Rmc1pp216 - 219 Yun-Liang Yang, Lei Guo, Shuang Xu, Christine A. Holland, Toshio Kitamura, Kent Hunter
& James M. Cunningham doi:10.1038/6005 Abstract|Full text|PDF
(175K)
Direct activation of TERT transcription by c-MYCpp220 - 224 Kou-Juey Wu, Carla Grandori, Mario Amacker, Nathalie Simon-Vermot, Axel Polack, Joachim Lingner
& Riccardo Dalla-Favera doi:10.1038/6010 Abstract|Full text|PDF
(502K)
Mice lacking link protein develop dwarfism and craniofacial abnormalities
pp225 - 229 Hideto Watanabe
& Yoshihiko Yamada doi:10.1038/6016 Abstract|Full text|PDF
(413K)
Localization of human BRCA1 and its loss in high-grade, non-inherited
breast carcinomaspp236 - 240 Cindy A. Wilson, Lillian Ramos, Maria R. Villaseñor, Karl H. Anders, Michael F. Press, Kathy Clarke, Beth Karlan, Jun-Jie Chen, Ralph Scully, David Livingston, Robert H. Zuch, Michael H. Kanter, Sylvan Cohen, Frank J. Calzone
& Dennis J. Slamon doi:10.1038/6029 Abstract|Full text|PDF
(468K)
Functional analysis of human MLH1 mutations in Saccharomyces cerevisiaep241 Hideki Shimodaira doi:10.1038/6036 Full text|PDF
(44K)
Genomic imprinting is disrupted in interspecific Peromyscus hybridsp241 Paul Vrana doi:10.1038/6066 Full text|PDF
(44K)
Mutations in the gene encoding gap junction protein −3 associated with autosomal dominant hearing impairmentp241 Jia-hi Xia doi:10.1038/6067 Full text|PDF
(44K)
Options available—from start to finish—for obtaining expression data by microarrayp241 David Bowtell doi:10.1038/6068 Full text|PDF
(44K)
subunit of phosphoinositide 3−kinase
−3 associated with autosomal dominant hearing impairment
