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Nature Genetics|October 16, 2002
Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humansKunio Kitamura, Masako Yanazawa, Noriyuki Sugiyama, et al.Nature Genetics|October 16, 2002
A role for the Rb family of proteins in controlling telomere lengthMarta García-Cao, Susana Gonzalo, Douglas Dean, et al.Nature Genetics|October 16, 2002
Sir2p and Sas2p opposingly regulate acetylation of yeast histone H4 lysine16 and spreading of heterochromatinNoriyuki Suka, Kunheng Luo, Michael GrunsteinNature Genetics|September 24, 2002
Mutations in Rab3a alter circadian period and homeostatic response to sleep loss in the mouseDavid Kapfhamer, Otto Valladares, Yi Sun, et al.Nature Genetics|May 29, 2002
Extensive genomic duplication during early chordate evolutionAoife McLysaght, Karsten Hokamp, Kenneth H WolfeNature Genetics|May 29, 2002
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene familyKarl P Schlingmann, Stefanie Weber, Melanie Peters, et al.Nature Genetics|May 29, 2002
Aberrant patterns of X chromosome inactivation in bovine clonesFei Xue, X Cindy Tian, Fuliang Du, et al.Nature Genetics|October 2, 2002
Genome-wide DNA replication profile for Drosophila melanogaster: a link between transcription and replication timingDirk Schübeler, David Scalzo, Charles Kooperberg, et al.Nature Genetics|October 2, 2002
Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomereRichard J L F Lemmers, Peggy de Kievit, Lodewijk Sandkuijl, et al.Nature Genetics|October 2, 2002
Human securin interacts with p53 and modulates p53-mediated transcriptional activity and apoptosisJuan A Bernal, Rosa Luna, Agueda Espina, et al.Pageof 742