The DNA sequence of the human X chromosome
暂无分享,去创建一个
David L. Steffen | R. Durbin | A. Coulson | J. Sulston | T. Andrews | N. Carter | M. Hurles | M. Metzker | R. Wilson | A. Frankish | S. Searle | C. Steward | A. Poustka | R. Fulton | L. Matthews | S. Whitehead | M. Dunn | P. Heath | S. Pelan | D. Grafham | G. Weinstock | R. Gibbs | H. Zoghbi | C. Clee | S. Hunt | D. Bentley | J. Mullikin | D. Willey | C. Cole | C. Rice | J. Rogers | L. Hillier | R. Waterston | A. Ciccodicola | D. Schlessinger | M. D'urso | H. Willard | A. Ballabio | L. Carrel | R. Gwilliam | D. Muzny | M. Morgan | S. Scherer | A. Hawes | A. Cree | H. Dinh | D. Wheeler | M. Ross | S. Pasternak | C. Bird | E. Sodergren | J. Burton | Matt Jones | K. McLay | B. Teague | R. David | S. Richards | K. Barlow | J. Davies | C. Langford | A. McMurray | P. Dhami | D. Swarbreck | J. Gilbert | K. Worley | T. Meitinger | H. Lehrach | P. Gunaratne | A. Hodgson | S. Gregory | D. Nelson | D. Beare | S. McLaren | Hua Shen | L. Lewis | R. Grocock | Yuan Chen | S. Gribble | S. Beck | R. Deadman | A. Dunham | A. Hunt | C. Lloyd | S. Milne | R. Shownkeen | P. Minx | A. Rosenthal | M. Platzer | G. Nyakatura | S. Taudien | J. Ramser | R. Reinhardt | G. Nordsiek | R. Connor | A. Fraser | E. Huckle | A. Beck | C. Chinault | G. Bethel | K. Evans | K. Howe | Patrick Meidl | S. Trevanion | S. Keenan | R. Storey | L. Wilming | C. Scott | J. Bye | Graham Scott | D. Steffen | P. Burch | O. Delgado | S. Dugan-Rocha | George R. Miner | Rachel B Gill | P. Havlak | Rui Chen | K. Durbin | P. Jong | M. Wall | A. West | C. Shaw-Smith | R. Banerjee | M. Leversha | J. Hume | N. Nguyen | E. Bruford | E. Chen | A. Meindl | M. Maheshwari | J. Loveland | J. Ashurst | R. Sudbrak | P. Galgóczy | A. Coffey | Yan Ding | S. Aradhya | C. Buhay | M. Ansari-Lari | A. Babbage | C. Bagguley | K. Bates | O. Beasley | A. M. Bridgeman | D. Buck | J. Burgess | C. Carder | S. Clegg | V. Cobley | N. Corby | S. Dodsworth | S. Ho | J. Kershaw | G. Laird | D. Lloyd | A. Pearce | D. Pearson | Y. Ramsey | H. Sehra | C. Skuce | R. Swann | M. Vaudin | M. N. Whiteley | L. Williams | H. Williamson | S. Hennig | K. Blechschmidt | K. Reichwald | S. Klages | F. Francis | K. Thomas | D. Villasana | P. Tabor | G. Howell | John Davis | A. Knights | G. Wen | R. Lozado | J. Warren | Jingkun Zhang | Dean Chavez | Clay Davis | G. Glöckner | Tim J. P. Hubbard | P. Wray | E. Hart | S. Rhodes | A. Tracey | Leni S. Jacob | Judith Hernandez | Ziad M Khan | David Parker | S. Palmer | K. Ambrose | H. Beasley | S. Bray-Allen | D. Burford | J. Chapman | S. Y. Clark | L. Faulkner | J. Frankland | C. Griffiths | P. J. Howden | S. Lawlor | J. Lovell | K. Porter | E. Sheridan | A. Thorpe | A. Tromans | Daniel Verduzco | D. Deshazo | Cerissa Hamilton | L. Waldron | Kerstin P. Clerc-Blankenburg | K. Timms | H. Loulseged | J. Yen | Michelle Smith | M. Ellwood | Rebecca Woodmansey | R. Pandian | J. McDowall | Wen Liu | Lesette M. Perez | C. Burrows | F. Lovell | A. Whittaker | R. Ainscough | R. Ashwell | Gary E. Barker | I. Barrett | N. Brady | Andrew J. Brown | M. J. Brown | David Bonnin | W. Burrill | Joseph Chako | Guan Chen | Zhijian Chen | G. Clarke | Karen Clifford | J. S. Conquer | H. Draper | I. Dutta | T. Eades | A. EMERY-COHEN | H. Errington | Yanghong Gu | K. Heitmann | B. Hinzmann | M. Hoffs | P. Hunt | J. Isherwood | David H. Johnson | S. Jones | S. Joseph | Susan H. Kelly | P. Kioschis | Anna Kosiura | Christie Kovar-Smith | Jing Lu | R. Lyne | Jie Ma | S. Mistry | Sidney Morris | I. Müller | C. N. O'Dell | G. Okwuonu | J. Parrish | D. Patel | Kerry A. Ridler | M. Schueler | E. Sotheran | H. E. Steingruber | T. Taylor | Qiaoyan Wang | G. Warry | Xuehong Wei | J. Wilkinson | Gabrielle A. Williams | A. Williamson | Jianling Zhou | S. Zorilla | C. L. Bagguley | J. K. Kershaw | A. V. Pearce | Matthew C. Jones | Paul E. Tabor | K. Clifford | S. Richards | S. Clark | P. Meidl | Ziad Khan | David Johnson | Brian Teague | C. O'Dell | Stuart McLaren | Katja Heitmann | R. Wilson | D. Muzny | Gary Barker | Rachel B. Gill | Stuart Mclaren | P. Howden | Andrew Cree | M. G. Schueler | D. DeShazo | Michael Hoffs | K. Evans | A. West
[1] M. Schartl,et al. First report on chicken genes and chromosomes 2000 , 2000, Cytogenetic and Genome Research.
[2] A. Federico,et al. MECP2 mutation in male patients with non‐specific X‐linked mental retardation , 2000, FEBS letters.
[3] P. Deloukas,et al. The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X , 2001, Nature.
[4] International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome , 2001, Nature.
[5] H. Zoghbi,et al. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 , 1999, Nature Genetics.
[6] D. Haussler,et al. A physical map of the human genome , 2001, Nature.
[7] M. A. Goldman,et al. Mammalian X chromosome inactivation. , 1992, Molecular genetic medicine.
[8] N. Takahata,et al. The amelogenin loci span an ancient pseudoautosomal boundary in diverse mammalian species , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[9] U. Francke. Digitized and differentially shaded human chromosome ideograms for genomic applications. , 1994, Cytogenetics and cell genetics.
[10] H. Willard,et al. X-inactivation profile reveals extensive variability in X-linked gene expression in females , 2005, Nature.
[11] H. Willard,et al. Physical and genetic mapping of the human X chromosome centromere: repression of recombination. , 1998, Genome research.
[12] Carolyn J. Brown,et al. The human XIST gene: Analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus , 1992, Cell.
[13] M. Daly,et al. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms , 2001, Nature.
[14] Jeannie T. Lee,et al. Tsix, a gene antisense to Xist at the X-inactivation centre , 1999, Nature Genetics.
[15] T. Graves,et al. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes , 2003, Nature.
[16] M. Lyon,et al. X-Chromosome inactivation: a repeat hypothesis , 1998, Cytogenetic and Genome Research.
[17] Horst Hameister,et al. Wide genome comparisons reveal the origins of the human X chromosome. , 2004, Trends in genetics : TIG.
[18] M. Lyon. Gene Action in the X-chromosome of the Mouse (Mus musculus L.) , 1961, Nature.
[19] Sam Griffiths-Jones,et al. The microRNA Registry , 2004, Nucleic Acids Res..
[20] H. Willard,et al. Analysis of the centromeric regions of the human genome assembly. , 2004, Trends in genetics : TIG.
[21] C. Helms,et al. Identification of a second pseudoautosomal region near the Xq and Yq telomeres. , 1992, Science.
[22] A. F. Scott,et al. OMIM: Online Mendelian Inheritance in Man , 2002 .
[23] P. Stankiewicz,et al. Genome architecture, rearrangements and genomic disorders. , 2002, Trends in genetics : TIG.
[24] L. Hurst. Evolutionary genomics: Sex and the X , 2001, Nature.
[25] J. Gécz,et al. Nonsyndromic X-linked mental retardation: where are the missing mutations? , 2003, Trends in genetics : TIG.
[26] Jack R. Davis,et al. Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene , 1998, Nature Genetics.
[27] R. Myers,et al. Quality assessment of the human genome sequence , 2004, Nature.
[28] I. Dunham,et al. The DNA sequence and analysis of human chromosome 6 , 2003, Nature.
[29] D. Haussler,et al. The structure and evolution of centromeric transition regions within the human genome , 2004, Nature.
[30] U. Surti,et al. Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28. , 1997, American journal of human genetics.
[31] Dr. Susumu Ohno. Sex Chromosomes and Sex-Linked Genes , 1967, Monographs on Endocrinology.
[32] Lior Pachter,et al. VISTA: computational tools for comparative genomics , 2004, Nucleic Acids Res..
[33] I. Dunham,et al. DNA sequence and analysis of human chromosome 9 , 2003, Nature.
[34] C. Disteche,et al. TSPY, the Candidate Gonadoblastoma Gene on the Human Y Chromosome, has a Widely Expressed Homologue on the X - Implications for Y Chromosome Evolution , 2004, Chromosome Research.
[35] B. Migeon,et al. Identification of TSIX, encoding an RNA antisense to human XIST, reveals differences from its murine counterpart: implications for X inactivation. , 2001, American journal of human genetics.
[36] Chuong B. Do,et al. Access the most recent version at doi: 10.1101/gr.926603 References , 2003 .
[37] A. Monaco,et al. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene , 1986, Nature.
[38] Lisa M. D'Souza,et al. Genome sequence of the Brown Norway rat yields insights into mammalian evolution , 2004, Nature.
[39] I. Scheffer,et al. Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy , 2002, Nature Genetics.
[40] N. Affara,et al. The sequence organization of Yp/proximal Xq homologous regions of the human sex chromosomes is highly conserved. , 1996, Genomics.
[41] J. Graves,et al. The minimal mammalian Y chromosome – the marsupial Y as a model system , 2001, Cytogenetic and Genome Research.
[42] D. Page,et al. A proposed path by which genes common to mammalian X and Y chromosomes evolve to become X inactivated , 1998, Nature.
[43] Colin N. Dewey,et al. Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution , 2004, Nature.
[44] Jean-Michel Claverie,et al. FusionDB: a database for in-depth analysis of prokaryotic gene fusion events , 2004, Nucleic Acids Res..
[45] A. Taylor,et al. The DNA sequence and comparative analysis of human chromosome 10 , 2004, Nature.
[46] Sean R. Eddy,et al. Rfam: an RNA family database , 2003, Nucleic Acids Res..
[47] A. Monaco,et al. Cloning the gene for an inherited human disorder—chronic granulomatous disease—on the basis of its chromosomal location , 1986, Nature.
[48] Carolyn J. Brown,et al. Characterization of expression at the human XIST locus in somatic, embryonal carcinoma, and transgenic cell lines. , 2003, Genomics.
[49] I. Dunham,et al. The DNA sequence and analysis of human chromosome 13 , 2004, Nature.
[50] K. Katz,et al. Introducing RefSeq and LocusLink: curated human genome resources at the NCBI. , 2000, Trends in genetics : TIG.
[51] A. Monaco,et al. Cloning the gene for the inherited disorder chronic granulomatous disease on the basis of its chromosomal location. , 1986, Cold Spring Harbor symposia on quantitative biology.
[52] Laurent Duret,et al. Comparative sequence analysis of the X-inactivation center region in mouse, human, and bovine. , 2000, Genome research.
[53] J. Graves. The origin and function of the mammalian Y chromosome and Y‐borne genes – an evolving understanding , 1995, BioEssays : news and reviews in molecular, cellular and developmental biology.
[54] J. R. MacDonald,et al. Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence , 2003, Genome Biology.
[55] D. Gudbjartsson,et al. A high-resolution recombination map of the human genome , 2002, Nature Genetics.
[56] T. Liesegang. The physical maps for sequencing human chromosomes 1,6,9,10,13,20 and X. Bentley DR,∗ Deloukas P, Dunham A, et al. Nature 2001;409:942–943. , 2001 .
[57] A. Simpson,et al. The cancer/testis genes: review, standardization, and commentary. , 2004, Cancer immunity.
[58] D R Bentley,et al. The DNA sequence and comparative analysis of human chromosome 20 , 2004, Nature.
[59] D. Page,et al. A human sex-chromosomal gene family expressed in male germ cells and encoding variably charged proteins. , 2000, Human molecular genetics.
[60] D. Botstein,et al. Occurrence of a transposition from the X-chromosome long arm to the Y-chromosome short arm during human evolution , 1984, Nature.
[61] J. Mullikin,et al. SSAHA: a fast search method for large DNA databases. , 2001, Genome research.
[62] S. Eddy,et al. tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. , 1997, Nucleic acids research.
[63] M. Bertrand,et al. An overview of the MAGE gene family with the identification of all human members of the family. , 2001, Cancer research.
[64] W. Earnshaw,et al. Co‐localization of centromere activity, proteins and topoisomerase II within a subdomain of the major human X α‐satellite array , 2002, The EMBO journal.
[65] A. Smit,et al. Ancestral, mammalian-wide subfamilies of LINE-1 repetitive sequences. , 1995, Journal of molecular biology.
[66] D. Page,et al. Four evolutionary strata on the human X chromosome. , 1999, Science.
[67] Carolyn J. Brown,et al. A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome , 1991, Nature.
[68] P. Pevzner,et al. Genome-scale evolution: reconstructing gene orders in the ancestral species. , 2002, Genome research.
[69] J A Bailey,et al. Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[70] E. Winzeler,et al. Genomic and Genetic Definition of a Functional Human Centromere , 2001, Science.
[71] A Collins,et al. CpG Islands in Human X‐Inactivation , 2003, Annals of human genetics.
[72] R. Allshire. Faculty Opinions recommendation of Co-localization of centromere activity, proteins and topoisomerase II within a subdomain of the major human X alpha-satellite array. , 2002 .
[73] J. V. Moran,et al. Initial sequencing and analysis of the human genome. , 2001, Nature.