Zobrazeno 1 - 3
of 3
pro vyhledávání: '"K. W. Jolly"'
Autor:
Michael A. Jarvis, C. L. Ziaja, C. M. Suzuki, D. J. DePianto, Charles F. Abildgaard, Jennifer Brown, Jerry S. Powell, K. W. Jolly, H. M. Reisner, Janet Harrison, L. G. Levin
Publikováno v:
Scopus-Elsevier
SummaryHemophilia A is a clotting disorder that is due to reduced or absent coagulation factor VIII (FVIII) activity. In approximately 25% of people with severe hemophilia A, standard treatment with intravenous plasma-derived or recombinant FVIII (rF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00005f3138fb8b073f3d791dbec67081
https://doi.org/10.1055/s-0038-1650268
https://doi.org/10.1055/s-0038-1650268
Autor:
M A, Jarvis, L G, Levin, J A, Harrison, D J, DePianto, C M, Suzuki, C L, Ziaja, J E, Brown, K W, Jolly, H M, Reisner, C F, Abildgaard, J S, Powell
Publikováno v:
Thrombosis and haemostasis. 75(2)
Hemophilia A is a clotting disorder that is due to reduced or absent coagulation factor VIII (FVIII) activity. In approximately 25% of people with severe hemophilia A, standard treatment with intravenous plasma-derived or recombinant FVIII (rFVIII) i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c9b9e674951e0f7f09f479ca6d3f02db
https://pubmed.ncbi.nlm.nih.gov/8815584
https://pubmed.ncbi.nlm.nih.gov/8815584
Publikováno v:
Oncogene. 9(1)
Germline mutations within evolutionary conserved exons of the p53 gene predispose to tumor development in several familial cancer syndromes. We now report identification of a novel p53 mutation affecting the splice acceptor site of exon 6 in the germ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f05b958d9fc8cb51cd109435d5e2d68c
https://pubmed.ncbi.nlm.nih.gov/8302608
https://pubmed.ncbi.nlm.nih.gov/8302608