Chromosome 21 and Down syndrome: from genomics to pathophysiology
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Stylianos E. Antonarakis | Emmanouil T. Dermitzakis | Alexandre Reymond | Robert Lyle | A. Reymond | E. Dermitzakis | S. Antonarakis | S. Deutsch | R. Lyle | Samuel Deutsch
[1] X. Estivill,et al. The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals. , 2000, Genome research.
[2] R. Aebersold,et al. Gene Expression Analyzed by High-resolution State Array Analysis and Quantitative Proteomics , 2004, Molecular & Cellular Proteomics.
[3] D. Cox,et al. Noncoding sequences conserved in a limited number of mammals in the SIM2 interval are frequently functional. , 2004, Genome research.
[4] Michael A Rogers,et al. Hair keratin associated proteins: characterization of a second high sulfur KAP gene domain on human chromosome 21. , 2004, The Journal of investigative dermatology.
[5] X. Estivill,et al. Murine models for Down syndrome , 2001, Physiology & Behavior.
[6] D. Cox,et al. Trisomy 21: Mechanisms and Models * , 1982, Annals of the New York Academy of Sciences.
[7] Mouse Genome Sequencing Consortium. Initial sequencing and comparative analysis of the mouse genome , 2002, Nature.
[8] C. Epstein. The Consequences of Chromosome Imbalance: The Consequences of Chromosome Imbalance , 1986 .
[9] William H. Majoros,et al. A Comparison of Whole-Genome Shotgun-Derived Mouse Chromosome 16 and the Human Genome , 2002, Science.
[10] P. Hunt,et al. To err (meiotically) is human: the genesis of human aneuploidy , 2001, Nature Reviews Genetics.
[11] Ruedi Aebersold,et al. Gene expression in yeast responding to mating pheromone: Analysis by high-resolution translation state analysis and quantitative proteomics , 2004 .
[12] D. Gudbjartsson,et al. A high-resolution recombination map of the human genome , 2002, Nature Genetics.
[13] Mark Gerstein,et al. Molecular fossils in the human genome: identification and analysis of the pseudogenes in chromosomes 21 and 22. , 2002, Genome research.
[14] C. Scriver,et al. The Metabolic and Molecular Bases of Inherited Disease, 8th Edition 2001 , 2001, Journal of Inherited Metabolic Disease.
[15] J. Lindstrom,et al. Alternate Stoichiometries of α4β2 Nicotinic Acetylcholine Receptors , 2003 .
[16] Yoshiyuki Sakaki,et al. A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 21q. , 2004, Genome research.
[17] S. Cawley,et al. Unbiased Mapping of Transcription Factor Binding Sites along Human Chromosomes 21 and 22 Points to Widespread Regulation of Noncoding RNAs , 2004, Cell.
[18] Ahmad Salehi,et al. Failed retrograde transport of NGF in a mouse model of Down's syndrome: Reversal of cholinergic neurodegenerative phenotypes following NGF infusion , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[19] C. V. Jongeneel,et al. Numerous potentially functional but non-genic conserved sequences on human chromosome 21 , 2002, Nature.
[20] J. Milunsky,et al. Genetic Disorders and the Fetus , 1988 .
[21] W. Kuo,et al. Detection of aneuploidy involving chromosomes 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes. , 1991, American journal of human genetics.
[22] M. Dierssen,et al. Impaired short- and long-term memory in Ts65Dn mice, a model for Down syndrome , 1998, Neuroscience Letters.
[23] J T Richtsmeier,et al. Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse. , 2000, Human molecular genetics.
[24] 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.
[25] R. Reeves,et al. Global disruption of the cerebellar transcriptome in a Down syndrome mouse model. , 2003, Human molecular genetics.
[26] Jonathan Pevsner,et al. Global up-regulation of chromosome 21 gene expression in the developing Down syndrome brain. , 2003, Genomics.
[27] Ajay N. Jain,et al. Assembly of microarrays for genome-wide measurement of DNA copy number , 2001, Nature Genetics.
[28] M. Oshimura,et al. Mice containing a human chromosome 21 model behavioral impairment and cardiac anomalies of Down's syndrome. , 2001, Human molecular genetics.
[29] Gregor Eichele,et al. Human chromosome 21 gene expression atlas in the mouse , 2002, Nature.
[30] A. Aguzzi,et al. Impaired Differentiation of Schwann Cells in Transgenic Mice with Increased PMP22 Gene Dosage , 1996, The Journal of Neuroscience.
[31] E. Niebuhr,et al. Down's syndrome , 1974, Humangenetik.
[32] S. Antonarakis,et al. Gene expression from the aneuploid chromosome in a trisomy mouse model of down syndrome. , 2004, Genome research.
[33] C. T. Morgan,et al. A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24. , 2003, Human molecular genetics.
[34] Pascal Kahlem,et al. A gene expression map of human chromosome 21 orthologues in the mouse , 2002, Nature.
[35] M. Farrer,et al. Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome? , 2000, Human Genetics.
[36] Alexandre Reymond,et al. Chromosome 21: a small land of fascinating disorders with unknown pathophysiology. , 2002, The International journal of developmental biology.
[37] D. Mccormick. Sequence the Human Genome , 1986, Bio/Technology.
[38] Bradley P. Coe,et al. A tiling resolution DNA microarray with complete coverage of the human genome , 2004, Nature Genetics.
[39] International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome , 2001, Nature.
[40] J. Schouten,et al. Rapid, high throughput prenatal detection of aneuploidy using a novel quantitative method (MLPA) , 2003, Journal of medical genetics.
[41] P. Simpson,et al. The choice of cell fate in the epidermis of Drosophila , 1991, Cell.
[42] H. Vijverberg,et al. Four Pharmacologically Distinct Subtypes of α4β2 Nicotinic Acetylcholine Receptor Expressed in Xenopus laevisOocytes , 1998 .
[43] J. Delabar,et al. Molecular Mapping of Twenty-Four Features of Down Syndrome on Chromosome 21 , 1993, European journal of human genetics : EJHG.
[44] J. Lupski,et al. Molecular mechanisms for genomic disorders. , 2003, Annual review of genomics and human genetics.
[45] T. Heffernan,et al. Partial IFN-alpha/beta and IFN-gamma receptor knockout trisomy 16 mouse fetuses show improved growth and cultured neuron viability. , 2000, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.
[46] G. Edelman,et al. Kinetics of homophilic binding by embryonic and adult forms of the neural cell adhesion molecule. , 1983, Proceedings of the National Academy of Sciences of the United States of America.
[47] T. Wiltshire,et al. Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21. , 2001, Genomics.
[48] L. Nadel,et al. The neuropsychology of Down syndrome: evidence for hippocampal dysfunction. , 2003, Child development.
[49] E. Birney,et al. Comparison of human chromosome 21 conserved nongenic sequences (CNGs) with the mouse and dog genomes shows that their selective constraint is independent of their genic environment. , 2004, Genome research.
[50] Katheleen Gardiner,et al. Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions. , 2003, Gene.
[51] M. Lovett,et al. Transgenic mice with increased Cu/Zn-superoxide dismutase activity: animal model of dosage effects in Down syndrome. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[52] K. Struhl,et al. The gradient morphogen bicoid is a concentration-dependent transcriptional activator , 1989, Cell.
[53] C J Epstein,et al. Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes , 2004, Developmental dynamics : an official publication of the American Association of Anatomists.
[54] S. Antonarakis,et al. Cell-type-specific and hypoxia-inducible expression of the human erythropoietin gene in transgenic mice. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[55] Shinsei Minoshima,et al. A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3. , 2004, Genomics.
[56] Mark J Alkema,et al. Transformation of axial skeleton due to overexpression of bmi-1 in transgenic mice , 1995, Nature.
[57] C. Epstein,et al. Genetic Dissection of Region Associated with Behavioral Abnormalities in Mouse Models for Down Syndrome , 2000, Pediatric Research.
[58] E. Kirkness,et al. The Dog Genome: Survey Sequencing and Comparative Analysis , 2003, Science.
[59] S. Cawley,et al. Novel RNAs identified from an in-depth analysis of the transcriptome of human chromosomes 21 and 22. , 2004, Genome research.
[60] R. Bronson,et al. A mouse model for Down syndrome exhibits learning and behaviour deficits , 1995, Nature Genetics.
[61] Nancy F. Hansen,et al. Comparative analyses of multi-species sequences from targeted genomic regions , 2003, Nature.
[62] B. Oostra,et al. A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly. , 2003, Human molecular genetics.
[63] K. Gardiner,et al. The sequence of human chromosome 21 and implications for research into Down syndrome , 2000, Genome Biology.
[64] M. Tymms,et al. Down's syndrome-like skeletal abnormalities in Ets2 transgenic mice , 1996, Nature.
[65] L. Shaffer,et al. Parental origin and timing of de novo Robertsonian translocation formation. , 2002, American journal of human genetics.
[66] L. Hartwell,et al. Normal stoichiometry of histone dimer sets is necessary for high fidelity of mitotic chromosome transmission , 1986, Cell.
[67] M. Adams,et al. Recent Segmental Duplications in the Human Genome , 2002, Science.
[68] S. Antonarakis. 10 years of Genomics, chromosome 21, and Down syndrome. , 1998, Genomics.
[69] D. Albertson,et al. Chromosome aberrations in solid tumors , 2003, Nature Genetics.
[70] C. V. Jongeneel,et al. Nineteen additional unpredicted transcripts from human chromosome 21. , 2002, Genomics.
[71] J. Bailey,et al. Patterns of meiotic recombination on the long arm of human chromosome 21. , 2000, Genome research.
[72] M. Hayden,et al. Human ABCA1 BAC Transgenic Mice Show Increased High Density Lipoprotein Cholesterol and ApoAI-dependent Efflux Stimulated by an Internal Promoter Containing Liver X Receptor Response Elements in Intron 1* , 2001, The Journal of Biological Chemistry.
[73] X. Estivill,et al. A high-resolution physical map of human chromosome 21p using yeast artificial chromosomes. , 1999, Genome research.
[74] S. P. Fodor,et al. Large-Scale Transcriptional Activity in Chromosomes 21 and 22 , 2002, Science.
[75] E. Zackai,et al. Down syndrome congenital heart disease: A narrowed region and a candidate gene , 2001, Genetics in Medicine.
[76] Alexandre Reymond,et al. Evolutionary Discrimination of Mammalian Conserved Non-Genic Sequences (CNGs) , 2003, Science.
[77] Anne-Marie Chang,et al. Functional Identification of the Mouse Circadian Clock Gene by Transgenic BAC Rescue , 1997, Cell.
[78] C. Disteche,et al. Down syndrome phenotypes: the consequences of chromosomal imbalance. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[79] C. Epstein. Mechanisms of the effects of aneuploidy in mammals. , 1988, Annual review of genetics.
[80] K. Gardiner,et al. Evolutionary breakpoints on human chromosome 21. , 2001, Genomics.
[81] C. Readhead,et al. Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage , 1994, Neuron.
[82] M T Davisson,et al. Segmental trisomy as a mouse model for Down syndrome. , 1993, Progress in clinical and biological research.
[83] M. Hattori,et al. The DNA sequence of human chromosome 21 , 2000, Nature.
[84] M. Davisson,et al. Motor dysfunction in a mouse model for Down syndrome , 1999, Physiology & Behavior.
[85] C. Epstein. The Consequences of Chromosome Imbalance: Principles, Mechanisms, and Models , 1986 .
[86] A. C. Chinault,et al. Charcot–Marie–Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit , 1992, Nature Genetics.
[87] C. Sismani,et al. Measurement of locus copy number by hybridisation with amplifiable probes. , 2000, Nucleic acids research.
[88] Jérôme Lejeune,et al. Etude des chromosomes somatiques de neuf enfants mongoliens. , 1959 .
[89] N. Hastie,et al. Transcriptome analysis of human autosomal trisomy. , 2002, Human molecular genetics.
[90] R G Worton,et al. Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' end. , 1988, Science.
[91] S. Malcolm,et al. Proteolipid protein gene dosage effect in Pelizaeus–Merzbacher disease , 1994, Nature Genetics.
[92] J T Richtsmeier,et al. Parallels of craniofacial maldevelopment in down syndrome and Ts65Dn mice , 2000, Developmental dynamics : an official publication of the American Association of Anatomists.
[93] S. P. Fodor,et al. Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21 , 2001, Science.
[94] M. Hattori,et al. DNA sequence and comparative analysis of chimpanzee chromosome 22 , 2004, Nature.
[95] S. South,et al. Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome. , 2004, Genome research.
[96] S. Antonarakis,et al. Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome. , 2000, Human molecular genetics.
[97] A. Reymond,et al. From PREDs and open reading frames to cDNA isolation: revisiting the human chromosome 21 transcription map. , 2001, Genomics.