Zobrazeno 1 - 10
of 105
pro vyhledávání: '"Bent, N"'
Autor:
Bent N (AUTHOR), Tennant A (AUTHOR), Swift T (AUTHOR), Posnett J (AUTHOR), Scuffham P (AUTHOR), Chamberlain MA (AUTHOR), Bent, N1 (AUTHOR), Tennant, A (AUTHOR), Swift, T (AUTHOR), Posnett, J (AUTHOR), Scuffham, P (AUTHOR), Chamberlain, M A (AUTHOR)
Publikováno v:
Lancet. 10/26/2002, Vol. 360 Issue 9342, p1280-1286. 7p.
Publikováno v:
South African Journal of Business Management. Dec2004, Vol. 35 Issue 4, p39-48. 10p. 10 Charts, 2 Graphs.
Akademický článek
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Autor:
Inge Thøger Christensen, David Neil Cooper, Flemming Jørgensen, Michael Krawczak, Niels Henrik Gregersen, Bent N. Terp, Peter Bross
Publikováno v:
Human Mutation. 20:98-109
The inclusion of a mutation in a pathology-based database such as the Human Gene Mutation Database (HGMD) is a two-stage process: first, the mutation must occur at the DNA level, then it must cause a clinically detectable disease state. The likelihoo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23a3e4e3d4752bb7d81420b68064f3da
https://doi.org/10.1002/humu.10095
https://doi.org/10.1002/humu.10095
Autor:
David Stuart Millar, Richard T. Wensley, Norma B. de Bosch, David Neil Cooper, Adrian Minford, Bent N. Johansen, Sam Schulman, Argimiro Torres, Vijay V. Kakkar, Paula H. B. Bolton-Maggs, Erik Berntorp
Publikováno v:
Human Genetics. 106:646-653
Severe protein C deficiency is a rare, early onset, venous thrombotic condition that is inherited as an autosomal recessive trait. The protein C (PROC) genes of nine unrelated individuals with severe protein C deficiency were sequenced yielding a tot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eacf896d721d57a37ad8e2830a2a8d7f
https://doi.org/10.1007/s004390000315
https://doi.org/10.1007/s004390000315
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Layla N. Al-Jader, Bent N. Johansen, Stephen Royston Palmer, David Neil Cooper, Peter S. Harper, Michael Krawczak
Publikováno v:
Human genetics. 108(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0df00cab05540549dcc977254de186b1
https://pubmed.ncbi.nlm.nih.gov/11214911
https://pubmed.ncbi.nlm.nih.gov/11214911
Autor:
Peter D. Stenson, David Neil Cooper, Nadia Chuzhanova, Bent N. Johansen, Edward V. Ball, Michael Krawczak
Publikováno v:
Scopus-Elsevier
No general rules have been proposed to account for the functional consequences of gene regulatory mutations. In a first attempt to establish the nature of such rules, an analysis was performed of the DNA sequence context of 153 different single base-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c62382833239101e4d3f5dd4c3c80e0
https://pubmed.ncbi.nlm.nih.gov/11129336
https://pubmed.ncbi.nlm.nih.gov/11129336
Autor:
Ole Mors, Anders D. Børglum, Ditte Demontis, Robert H. Yolken, Carsten Bøcker Pedersen, Bent N. Petersen, David M. Hougaard, Preben Bo Mortensen
Publikováno v:
Schizophrenia Research. 117:181
Simona A. Stilo, Craig Morgan, Clare Flach, Alessandra Paparelli, Paola Casadio, Jennifer O'Connor, Manuela Russo, Ben Wiffen, Aurora M. Falcone, Candice Joseph, Tiago Reis Marques, Valeria Mondelli, Grant McQueen, Paola Dazzan, Marta Di Forti, Robin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cda8004b6afef5385a083ea0a79fe4a
https://doi.org/10.1016/j.schres.2010.02.222
https://doi.org/10.1016/j.schres.2010.02.222