The DNA sequence and comparative analysis of human chromosome 10

Autor: P, Deloukas, M E, Earthrowl, D V, Grafham, M, Rubenfield, L, French, C A, Steward, S K, Sims, M C, Jones, S, Searle, C, Scott, K, Howe, S E, Hunt, T D, Andrews, J G R, Gilbert, D, Swarbreck, J L, Ashurst, A, Taylor, J, Battles, C P, Bird, R, Ainscough, J P, Almeida, R I S, Ashwell, K D, Ambrose, A K, Babbage, C L, Bagguley, J, Bailey, R, Banerjee, K, Bates, H, Beasley, S, Bray-Allen, A J, Brown, J Y, Brown, D C, Burford, W, Burrill, J, Burton, P, Cahill, D, Camire, N P, Carter, J C, Chapman, S Y, Clark, G, Clarke, C M, Clee, S, Clegg, N, Corby, A, Coulson, P, Dhami, I, Dutta, M, Dunn, L, Faulkner, A, Frankish, J A, Frankland, P, Garner, J, Garnett, S, Gribble, C, Griffiths, R, Grocock, E, Gustafson, S, Hammond, J L, Harley, E, Hart, P D, Heath, T P, Ho, B, Hopkins, J, Horne, P J, Howden, E, Huckle, C, Hynds, C, Johnson, D, Johnson, A, Kana, M, Kay, A M, Kimberley, J K, Kershaw, M, Kokkinaki, G K, Laird, S, Lawlor, H M, Lee, D A, Leongamornlert, G, Laird, C, Lloyd, D M, Lloyd, J, Loveland, J, Lovell, S, McLaren, K E, McLay, A, McMurray, M, Mashreghi-Mohammadi, L, Matthews, S, Milne, T, Nickerson, M, Nguyen, E, Overton-Larty, S A, Palmer, A V, Pearce, A I, Peck, S, Pelan, B, Phillimore, K, Porter, C M, Rice, A, Rogosin, M T, Ross, T, Sarafidou, H K, Sehra, R, Shownkeen, C D, Skuce, M, Smith, L, Standring, N, Sycamore, J, Tester, A, Thorpe, W, Torcasso, A, Tracey, A, Tromans, J, Tsolas, M, Wall, J, Walsh, H, Wang, K, Weinstock, A P, West, D L, Willey, S L, Whitehead, L, Wilming, P W, Wray, L, Young, Y, Chen, R C, Lovering, N K, Moschonas, R, Siebert, K, Fechtel, D, Bentley, R, Durbin, T, Hubbard, L, Doucette-Stamm, S, Beck, D R, Smith, J, Rogers

Publikováno v: Nature. 429:375-381

The finished sequence of human chromosome 10 comprises a total of 131,666,441 base pairs. It represents 99.4% of the euchromatic DNA and includes one megabase of heterochromatic sequence within the pericentromeric region of the short and long arm of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::246ea455e51f911c6f69c0cba33ba990
https://doi.org/10.1038/nature02462

Locus assignment of human alpha-globin structural mutants by selective enzymatic amplification of alpha 1 and alpha 2-globin cDNAs

Autor: A, Mamalaki, M, Horanyi, J, Szelenyi, N K, Moschonas

Publikováno v: Human genetics. 85(5)

We have used the powerful methodology of DNA enzymatic amplification in order to assign human alpha-globin structural mutants to one of the two highly homologous alpha-globin genes. Selectively amplified alpha 1 and alpha 2-globin cDNAs were dot-blot

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2869bffc785ecaf614e2d03184532b92
https://pubmed.ncbi.nlm.nih.gov/2227935

European Gene Mapping Project (EUROGEM): Breakpoint panels for human chromosomes based on the CEPH reference families

Autor: S. A. COX, J. ATTWOOD, S. P. BRYANT, R. BAINS, S. POVEY, M. REBELLO, M. KAPSETAKI, N. K. MOSCHONAS, K.-H. GRZESCHIK, M. OTTO, M. DIXON, H. E. SUDWORTH, R. F. KOOY, A. WRIGHT, P. TEAGUE, L. TERRENATO, G. VERGNAUD, S. MONFOUILLOUX, J. WEISSENBACH, O. ALIBERT, C. DIB, S. FAURÉ, E. BARKER, N. M. PEARSON, R. H. A. M. VOSSEN, A. GAL, B. MUELLER-MYHSOK, H. M. CANN, N. K. SPURR

Publikováno v: Scopus-Elsevier
Annals of Human Genetics, 60, 447-486. Wiley

Meiotic breakpoint panels for human chromosomes 2, 3, 4, 5, 6, 7, 8, 9, 10, 13, 14, 15, 17, 18, 20 and X were constructed from genotypes from the CEPH reference families. Each recombinant chromosome included has a breakpoint well-supported with refer

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8afda11e76b1e6bc492579cfbda057c3
http://www.scopus.com/inward/record.url?eid=2-s2.0-12644260443&partnerID=MN8TOARS