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Proceedings of the National Academy of Sciences of the United States of America|October 1, 1986
Isolation of an episomal yeast gene and replication origin as chromatinD S Pederson, M Venkatesan, F Thoma, et al.
Carcinogenesis|November 1, 1987
Ascorbate potentiates DNA damage by 1-methyl-1-nitrosourea in vivo and generates DNA strand breaks in vitroP V Woolley, S Kumar, P Fitzgerald, et al.
The Journal of Biological Chemistry|April 25, 1992
The role of the first growth factor domain of human factor IXa in binding to platelets and in factor X activationS S Ahmad, R Rawala-Sheikh, W F Cheung, et al.
The Journal of Clinical Investigation|November 1, 1991
Factor XSanto Domingo. Evidence that the severe clinical phenotype arises from a mutation blocking secretionH H Watzke, A Wallmark, N Hamaguchi, et al.
Blood|February 15, 1989
Molecular defect in factor IXHilo, a hemophilia Bm variant: Arg----Gln at the carboxyterminal cleavage site of the activation peptideM N Huang, C K Kasper, H R Roberts, et al.
Biochemistry|September 28, 1998
Role of the propeptide and gamma-glutamic acid domain of factor IX for in vitro carboxylation by the vitamin K-dependent carboxylaseT B Stanley, S M Wu, R J Houben, et al.
Blood|July 1, 1989
Molecular cloning of a cDNA encoding canine factor IXJ P Evans, H H Watzke, J L Ware, et al.
Blood|December 9, 1998
A missense mutation in gamma-glutamyl carboxylase gene causes combined deficiency of all vitamin K-dependent blood coagulation factorsB Brenner, B Sánchez-Vega, S M Wu, et al.
Blood|January 1, 1987
Factor IXAlabama: a point mutation in a clotting protein results in hemophilia BL M Davis, R A McGraw, J L Ware, et al.
Clinics in Haematology|June 1, 1985
Structure and function of factor IX: defects in haemophilia BR A McGraw, L M Davis, R L Lundblad, et al.
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