CHAPTER 10 – Inter-Species Comparative Sequence Analysis: A Tool for Genomic Medicine
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[1] William Stafford Noble,et al. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project , 2007, Nature.
[2] M. McCarthy,et al. Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes , 2007, Science.
[3] G. Abecasis,et al. A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants , 2007, Science.
[4] O. Cockerell,et al. Connexin 32 promoter P2 mutations: A mechanism of peripheral nerve dysfunction , 2004, Clinical Neurophysiology.
[5] S. Pääbo,et al. Accelerated Evolution of Conserved Noncoding Sequences in Humans , 2006, Science.
[6] C. Ponting,et al. Evolutionary biology: Human brain gene wins genome race , 2006, Nature.
[7] D. Haussler,et al. An RNA gene expressed during cortical development evolved rapidly in humans , 2006, Nature.
[8] A. Smit,et al. Functional noncoding sequences derived from SINEs in the mammalian genome. , 2006, Genome research.
[9] E. Lander,et al. A large family of ancient repeat elements in the human genome is under strong selection. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[10] R. Kelsh,et al. Deletion of long-range sequences at Sox10 compromises developmental expression in a mouse model of Waardenburg-Shah (WS4) syndrome. , 2006, Human molecular genetics.
[11] Alexander E. Kel,et al. TRANSFAC® and its module TRANSCompel®: transcriptional gene regulation in eukaryotes , 2005, Nucleic Acids Res..
[12] Shyam Prabhakar,et al. Close sequence comparisons are sufficient to identify human cis-regulatory elements. , 2005, Genome research.
[13] James A. Cuff,et al. Genome sequence, comparative analysis and haplotype structure of the domestic dog , 2005, Nature.
[14] Jean L. Chang,et al. Initial sequence of the chimpanzee genome and comparison with the human genome , 2005, Nature.
[15] E. Grice,et al. A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk , 2005, Nature.
[16] C. Plessy,et al. Enhancer sequence conservation between vertebrates is favoured in developmental regulator genes. , 2005, Trends in genetics : TIG.
[17] D. Altshuler,et al. Harvesting Medical Information from the Human Family Tree , 2005, Science.
[18] Colin N. Dewey,et al. Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution , 2004, Nature.
[19] E. Lander,et al. Finishing the euchromatic sequence of the human genome , 2004 .
[20] Lior Pachter,et al. VISTA: computational tools for comparative genomics , 2004, Nucleic Acids Res..
[21] Antony V. Cox,et al. The Ensembl Web site: mechanics of a genome browser. , 2004, Genome research.
[22] Lisa M. D'Souza,et al. Genome sequence of the Brown Norway rat yields insights into mammalian evolution , 2004, Nature.
[23] David B. Goldstein,et al. Pharmacogenetics goes genomic , 2003, Nature Reviews Genetics.
[24] D. Haussler,et al. Article Identification and Characterization of Multi-Species Conserved Sequences , 2022 .
[25] Mei Li,et al. MultiPipMaker and supporting tools: alignments and analysis of multiple genomic DNA sequences , 2003, Nucleic Acids Res..
[26] F. Collins,et al. A vision for the future of genomics research , 2003, Nature.
[27] D. Church,et al. Cross-species sequence comparisons: a review of methods and available resources. , 2003, Genome research.
[28] Colin N. Dewey,et al. Initial sequencing and comparative analysis of the mouse genome. , 2002 .
[29] Minerva M. Carrasquillo,et al. Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease , 2002, Nature Genetics.
[30] Paramvir S. Dehal,et al. Whole-Genome Shotgun Assembly and Analysis of the Genome of Fugu rubripes , 2002, Science.
[31] Tom H. Pringle,et al. The human genome browser at UCSC. , 2002, Genome research.
[32] W. J. Kent,et al. BLAT--the BLAST-like alignment tool. , 2002, Genome research.
[33] S. Dheen,et al. Retinoic acid influences Phox2 expression of cardiac ganglionic cells in the developing rat heart , 2002, Neuroscience Letters.
[34] O. Dubourg,et al. Human Connexin 32, a gap junction protein altered in the X-linked form of Charcot-Marie-Tooth disease, is directly regulated by the transcription factor SOX10. , 2001, Human molecular genetics.
[35] M. Tzetis,et al. Qualitative and quantitative analysis of mRNA associated with four putative splicing mutations (621+3A→G, 2751+2T→A, 296+1G→C, 1717–9T→C-D565G) and one nonsense mutation (E822X) in the CFTR gene , 2001, Human Genetics.
[36] Joseph H. Nadeau,et al. Modifier genes in mice and humans , 2001, Nature Reviews Genetics.
[37] J. V. Moran,et al. Initial sequencing and analysis of the human genome. , 2001, Nature.
[38] E. Batourina,et al. Vitamin A controls epithelial/mesenchymal interactions through Ret expression , 2001, Nature Genetics.
[39] W. Miller,et al. Identification of a coordinate regulator of interleukins 4, 13, and 5 by cross-species sequence comparisons. , 2000, Science.
[40] R. Gibbs,et al. PipMaker--a web server for aligning two genomic DNA sequences. , 2000, Genome research.
[41] J. Thompson,et al. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. , 1994, Nucleic acids research.
[42] J. Hartman,et al. Cystic fibrosis transmembrane conductance regulator mutations that disrupt nucleotide binding. , 1994, The Journal of clinical investigation.
[43] V. Ionasescu,et al. Point mutations of the connexin32 (GJB1) gene in X-linked dominant Charcot-Marie-Tooth neuropathy. , 1994, Human molecular genetics.
[44] B. Ponder,et al. Mutations of the RET proto-oncogene in Hirschsprung's disease , 1994, Nature.
[45] Charles Elkan,et al. Fitting a Mixture Model By Expectation Maximization To Discover Motifs In Biopolymer , 1994, ISMB.
[46] A. Harris,et al. Abnormal mRNA splicing resulting from three different mutations in the CFTR gene. , 1993, Human molecular genetics.
[47] M. Welsh,et al. Regulation by ATP and ADP of CFTR chloride channels that contain mutant nucleotide-binding domains. , 1992, Science.
[48] E. Myers,et al. Basic local alignment search tool. , 1990, Journal of molecular biology.
[49] L. Tsui,et al. Erratum: Identification of the Cystic Fibrosis Gene: Genetic Analysis , 1989, Science.
[50] L. Tsui,et al. Erratum: Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA , 1989, Science.
[51] J. Riordan,et al. Identification of the Cystic Fibrosis Gene : Chromosome Walking and Jumping Author ( s ) : , 2008 .