Recombinant DNA methods in hemophilia A : carrier detection and prenatal diagnosisSADLER, J. E.Seminars in thrombosis and hemostasis. 1990, Vol 16, Num 4, pp 341-347, issn 0094-6176, 7 p.Article

Von Willebrand disease : a database of point mutations, insertions, and deletions : for the consortium on von Willebrand Factor Mutations and Polymorphisms, and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and HaemostasisGINSBURG, D; SADLER, J. E.Thrombosis and haemostasis. 1993, Vol 69, Num 2, pp 177-184, issn 0340-6245Article

A database of polymorphisms in the von Willebrand factor gene and pseudogene : for the consortium on von Willebrand Factor Mutations and Polymorphisms, and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and HaemostasisSADLER, J. E; GINSBURG, D.Thrombosis and haemostasis. 1993, Vol 69, Num 2, pp 185-191, issn 0340-6245Article

Regulation of endothelial cell coagulant properties: modulation of tissue factor, plasminogen activator inhibitors, and thrombomodulin by phorbol 12-myristate 13-acetate and tumor necrosis factorSCARPATI, E; SADLER, J. E.The Journal of biological chemistry (Print). 1989, Vol 264, Num 34, pp 20705-20713, issn 0021-9258Article

Impact, diagnosis and treatment of von Willebrand DiseaseSADLER, J. E; MANNUCCI, P. M; BERNTORP, E et al.Thrombosis and haemostasis. 2000, Vol 84, Num 2, pp 160-174, issn 0340-6245Article

The mutation Arg (53) → Trp causes von Willebrand disease Normandy by abolishing binding to factor VIII. Studies with recombinant von Willebrand factorJORIEUX, S; TULEY, E. A; GAUCHER, C et al.Blood. 1992, Vol 79, Num 3, pp 563-567, issn 0006-4971Article

Characterization of three mutations causing von Willebrand disease type IIA in five unrelated familiesINBAL, A; SELIGSOHN, U; KORNBROT, N et al.Thrombosis and haemostasis. 1992, Vol 67, Num 6, pp 618-622, issn 0340-6245Article

Recombinant von Willebrand factor Arg⁵⁷⁸→Gln : a type IIB von Willebrand disease mutation affects binding to glycoprotein Ib but not to collagen or heparinRANDI, A. M; JORIEUX, S; TULEY, E. A et al.The Journal of biological chemistry (Print). 1992, Vol 267, Num 29, pp 21187-21192, issn 0021-9258Article

Induction of specific storage organelles by von Willebrand factor propolypeptideWAGNER, D. D; SAFFARIPOUR, S; BONFANTI, R et al.Cell (Cambridge). 1991, Vol 64, Num 2, pp 403-413, issn 0092-8674, 11 p.Article

The structure and function of mouse thrombomodulin: phorbol myristate acetate stimulates degradation and synthesis of thrombomodulin without affecting mRNA levels in hemangioma cellsDITTMAN, W. A; KUMADA, T; SADLER, J. E et al.The Journal of biological chemistry (Print). 1988, Vol 263, Num 30, pp 15815-15822, issn 0021-9258Article

Structure of murine enterokinase (enteropeptidase) and expression in small intestine during developmentXIN YUAN; XINGLONG ZHENG; DESHUN LU et al.American journal of physiology. Gastrointestinal and liver physiology. 1998, Vol 37, Num 2, pp G342-G348, issn 0193-1857Article

Designing silo walls for flow patternsSADLER, J. E; JOHNSTON, F. T; MAHMOUD, M. H et al.ACI structural journal. 1995, Vol 92, Num 2, pp 219-228, issn 0889-3241Article

Disulfide bonds required to assemble functional von Willebrand factor multimersZHENGYU DONG; THOMA, R. S; CRIMMINS, D. L et al.The Journal of biological chemistry (Print). 1994, Vol 269, Num 9, pp 6753-6758, issn 0021-9258Article

Effects of cellular transformation on expression of plasminogen activator inhibitors 1 and 2: evidence for independent regulationCOHEN, R. L; NICLAS, J; LEE, W. M. F et al.The Journal of biological chemistry (Print). 1989, Vol 264, Num 14, pp 8375-8383, issn 0021-9258Article

Mammalian protein secretion without signal peptide removal: biosynthesis of plasminogen activator inhibitor-2 in U-937 cellsYE, R. D; TZE-CHEIN WUN; SADLER, J. E et al.The Journal of biological chemistry (Print). 1988, Vol 263, Num 10, pp 4869-4875, issn 0021-9258Article

cDNA cloning and expression in Escherichia coli of a plasminogen activator inhibitor from human placentaYE, R. D; TZE-CHEIN WUN; SADLER, J. E et al.The Journal of biological chemistry (Print). 1987, Vol 262, Num 8, pp 3718-3725, issn 0021-9258Article

Amino acid sequence of human von Willebrand factorTITANI, K; KUMAR, S; TAKIO, K et al.Biochemistry (Easton). 1986, Vol 25, Num 11, pp 3171-3184, issn 0006-2960Article

Regulation of human tissue factor expression by mRNA turnoverAHERN, S. M; MIYATA, T; SADLER, J. E et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 3, pp 2154-2159, issn 0021-9258Article

Sequences required for thrombomodulin cofactor activity within the fourth epidermal growth factor-like domain of human thrombomodulinLENTZ, S. R; YAN CHEN; SADLER, J. E et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 20, pp 15312-15317, issn 0021-9258Article

Inhibition of thrombomodulin surface expression and protein C activation by the thrombogenic agent homocysteineLENTZ, S. R; SADLER, J. E.The Journal of clinical investigation. 1991, Vol 88, Num 6, pp 1906-1914, issn 0021-9738Article

Homocysteine inhibits von Willebrand factor processing and secretion by preventing transport from the endoplasmic reticulumLENTZ, S. R; SADLER, J. E.Blood. 1993, Vol 81, Num 3, pp 683-689, issn 0006-4971Article

Acquired von Willebrand syndrome : Data from an International registryFEDERICI, A. B; RAND, J. H; BUCCIARELLI, P et al.Thrombosis and haemostasis. 2000, Vol 84, Num 2, pp 345-349, issn 0340-6245Article

Type 2M von Willebrand disease : F606I and 1662F mutations in the glycoprotein ib binding domain selectively impair ristocetin- but not botrocetin-mediated binding of von Willebrand factor to plateletsHILLERY, C. A; MANCUSO, D. J; SADLER, J. E et al.Blood. 1998, Vol 91, Num 5, pp 1572-1581, issn 0006-4971Article

Molecular mechanism and classification of von Willebrand diseaseSADLER, J. E; MATSUSHITA, T; ZHENGYU DONG et al.Thrombosis and haemostasis. 1995, Vol 74, Num 1, pp 161-166, issn 0340-6245Conference Paper

Refractory immune hemolytic anemia with a high thermal amplitude, low affinity IgG anti-Pr_a cold autoantibodyRAMOS, R. R; CURTIS, B. R; SADLER, J. E et al.Autoimmunity (Print). 1992, Vol 12, Num 2, pp 149-154, issn 0891-6934Article