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Journal Articles

The role of amino-terminal residues of the heavy chain of factor IXa in the binding of its cofactor, factor VIIIa

N Hamaguchi, SP Bajaj, KJ Smith, DW Stafford

Blood (1994) 84 (6): 1837–1842.

https://doi.org/10.1182/blood.V84.6.1837.1837

Published: 1994

Journal Articles

Mapping of monoclonal antibodies to human factor IX

D Frazier, KJ Smith, WF Cheung, J Ware, SW Lin, AR Thompson, H Reisner, SP Bajaj, DW Stafford

Blood (1989) 74 (3): 971–977.

https://doi.org/10.1182/blood.V74.3.971.971

Published: 1989

Journal Articles

Molecular cloning of a cDNA encoding canine factor IX

JP Evans, HH Watzke, JL Ware, DW Stafford, KA High

Blood (1989) 74 (1): 207–212.

https://doi.org/10.1182/blood.V74.1.207.207

Published: 1989

Journal Articles

Molecular defect in factor IXHilo, a hemophilia Bm variant: Arg----Gln at the carboxyterminal cleavage site of the activation peptide

MN Huang, CK Kasper, HR Roberts, DW Stafford, KA High

Blood (1989) 73 (3): 718–721.

https://doi.org/10.1182/blood.V73.3.718.718

Published: 1989

Journal Articles

Identification of a F.VIII epitope recognized by a human hemophilic inhibitor

BC Lubahn, J Ware, DW Stafford, HM Reisner

Blood (1989) 73 (2): 497–499.

https://doi.org/10.1182/blood.V73.2.497.497

Published: 1989

Journal Articles

Genetic defect responsible for the dysfunctional protein: factor IXLong Beach

J Ware, L Davis, D Frazier, SP Bajaj, DW Stafford

Blood (1988) 72 (2): 820–822.

https://doi.org/10.1182/blood.V72.2.820.820

Published: 1988

Journal Articles

Factor IXAlabama: a point mutation in a clotting protein results in hemophilia B

LM Davis, RA McGraw, JL Ware, HR Roberts, DW Stafford

Blood (1987) 69 (1): 140–143.

https://doi.org/10.1182/blood.V69.1.140.140

Published: 1987

NARROW

The role of amino-terminal residues of the heavy chain of factor IXa in the binding of its cofactor, factor VIIIa

Mapping of monoclonal antibodies to human factor IX

Molecular cloning of a cDNA encoding canine factor IX

Molecular defect in factor IXHilo, a hemophilia Bm variant: Arg----Gln at the carboxyterminal cleavage site of the activation peptide

Identification of a F.VIII epitope recognized by a human hemophilic inhibitor

Genetic defect responsible for the dysfunctional protein: factor IXLong Beach

Factor IXAlabama: a point mutation in a clotting protein results in hemophilia B

Email alerts

ASH Publications

American Society of Hematology

The role of amino-terminal residues of the heavy chain of factor IXa in the binding of its cofactor, factor VIIIa

Mapping of monoclonal antibodies to human factor IX

Molecular cloning of a cDNA encoding canine factor IX

Molecular defect in factor IXHilo, a hemophilia Bm variant: Arg----Gln at the carboxyterminal cleavage site of the activation peptide

Identification of a F.VIII epitope recognized by a human hemophilic inhibitor

Genetic defect responsible for the dysfunctional protein: factor IXLong Beach

Factor IXAlabama: a point mutation in a clotting protein results in hemophilia B

Email alerts

ASH Publications

American Society of Hematology

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