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pro vyhledávání: '"Launchbury, RJ"'
Autor:
Campbell, AJ, Lyne, L, Brown, PJ, Launchbury, RJ, Bignone, P, Chi, J, Roncador, G, Lawrie, CH, Gatter, KC, Kusec, R, Banham, AH
FOXP2 mutation causes a severe inherited speech and language defect, while the related transcription factors FOXP1, FOXP3 and FOXP4 are implicated in cancer. FOXP2 mRNA and protein expression were characterised in normal human tissues, haematological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9ed8bdf92da0f7aa05434032bf486385
https://ora.ox.ac.uk/objects/uuid:c03b65e1-72f9-4dde-a42e-14d317dc67c8
https://ora.ox.ac.uk/objects/uuid:c03b65e1-72f9-4dde-a42e-14d317dc67c8
Autor:
Campbell AJ; Nuffield Department of Clinical Laboratory Sciences, University of Oxford, John Radcliffe Hospital, Oxford, UK., Lyne L, Brown PJ, Launchbury RJ, Bignone P, Chi J, Roncador G, Lawrie CH, Gatter KC, Kusec R, Banham AH
Publikováno v:
British journal of haematology [Br J Haematol] 2010 Apr; Vol. 149 (2), pp. 221-30. Date of Electronic Publication: 2010 Jan 20.