Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions.
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Katheleen Gardiner | K. Gardiner | M. Davisson | L. Bechtel | A. Fortna | Muriel T Davisson | Andrew Fortna | Lawrence Bechtel
[1] B. Agranoff,et al. Advances in Neurochemistry , 1977, Advances in Neurochemistry.
[2] C. Gissi,et al. Structural and functional features of eukaryotic mRNA untranslated regions. , 2001, Gene.
[3] T. Wiltshire,et al. Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21. , 2001, Genomics.
[4] C. Epstein,et al. Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits learning and behavioral abnormalities. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[5] N. Harris,et al. Genotator: a workbench for sequence annotation. , 1997, Genome research.
[6] L. Nadel,et al. The neuropsychology of Down syndrome: evidence for hippocampal dysfunction. , 2003, Child development.
[7] Colin N. Dewey,et al. Initial sequencing and comparative analysis of the mouse genome. , 2002 .
[8] M. Hattori,et al. The DNA sequence of human chromosome 21 , 2000, Nature.
[9] P. Jacobs,et al. Trisomy in man. , 1984, Annual review of genetics.
[10] Pascal Kahlem,et al. A gene expression map of human chromosome 21 orthologues in the mouse , 2002, Nature.
[11] K. Gardiner,et al. Genomic sequence analysis tools: a user's guide. , 2001, Trends in genetics : TIG.
[12] Emmanuel Dias-Neto,et al. The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[13] William H. Majoros,et al. A Comparison of Whole-Genome Shotgun-Derived Mouse Chromosome 16 and the Human Genome , 2002, Science.
[14] M. Ventura,et al. Juxtacentromeric region of human chromosome 21: a boundary between centromeric heterochromatin and euchromatic chromosome arms. , 2003, Gene.
[15] K. Gardiner,et al. Annotation of human chromosome 21 for relevance to Down syndrome: gene structure and expression analysis. , 2002, Genomics.
[16] W. Tam. Identification and characterization of human BIC, a gene on chromosome 21 that encodes a noncoding RNA. , 2001, Gene.
[17] M. Davisson. Mouse models of Down syndrome , 2005 .
[18] M. Hattori,et al. Identification of two novel primate-specific genes in DSCR. , 2002, DNA research : an international journal for rapid publication of reports on genes and genomes.
[19] K. Gardiner,et al. Ts65Dn – localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome , 2001, Cytogenetic and Genome Research.
[20] E. Birney,et al. Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs , 2002, Nature.
[21] A. Reymond,et al. From PREDs and open reading frames to cDNA isolation: revisiting the human chromosome 21 transcription map. , 2001, Genomics.
[22] M. Suyama,et al. HUGE: a database for human large proteins identified in the Kazusa cDNA sequencing project. , 2000, Nucleic acids research.
[23] C. Scriver,et al. The Metabolic and Molecular Bases of Inherited Disease, 8th Edition 2001 , 2001, Journal of Inherited Metabolic Disease.
[24] C. V. Jongeneel,et al. Nineteen additional unpredicted transcripts from human chromosome 21. , 2002, Genomics.
[25] Shinsei Minoshima,et al. Erratum: The DNA sequence of human chromosome 21: The chromosome 21 mapping and sequencing consortium (Nature (2000) 405 (311-319)) , 2000 .
[26] Gregor Eichele,et al. Human chromosome 21 gene expression atlas in the mouse , 2002, Nature.
[27] R. Gibbs,et al. PipMaker--a web server for aligning two genomic DNA sequences. , 2000, Genome research.
[28] S. P. Fodor,et al. Large-Scale Transcriptional Activity in Chromosomes 21 and 22 , 2002, Science.
[29] M. Soares,et al. Normalization and subtraction: two approaches to facilitate gene discovery. , 1996, Genome research.
[30] C. Epstein,et al. Genetic Dissection of Region Associated with Behavioral Abnormalities in Mouse Models for Down Syndrome , 2000, Pediatric Research.