Theodore S. Zimmerman
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Theodore S. Zimmermanphilosophy Degrees
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Theodore S. Zimmermanbiology Degrees
Biology
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Biochemistry
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Philosophy Biology
Theodore S. Zimmerman's Degrees
- Masters Medicine University of California, San Francisco
- PhD Biochemistry University of California, San Francisco
Why Is Theodore S. Zimmerman Influential?
(Suggest an Edit or Addition)Theodore S. Zimmerman's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Deficiency of protein C in congenital thrombotic disease. (1981) (1306)
- Immunologic differentiation of classic hemophilia (factor 8 deficiency) and von Willebrand's dissase, with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V) and on an acquired circulating anticoagulant against antihemophilic factor. (1971) (586)
- Deamino-8-D-arginine vasopressin shortens the bleeding time in uremia. (1983) (573)
- Variant von Willebrand's disease: characterization of two subtypes by analysis of multimeric composition of factor VIII/von Willebrand factor in plasma and platelets. (1980) (534)
- Heightened interaction between platelets and factor VIII/von Willebrand factor in a new subtype of von Willebrand's disease. (1980) (395)
- The complex multimeric composition of factor VIII/von Willebrand factor. (1981) (371)
- Proteolytic inactivation of human factor VIII procoagulant protein by activated human protein C and its analogy with factor V. (1984) (306)
- The complex multimeric composition of factor VIII/von Willebrand factor (1981) (303)
- von Willebrand factor and von Willebrand disease. (1987) (279)
- von Willebrand factor. A reduced and alkylated 52/48-kDa fragment beginning at amino acid residue 449 contains the domain interacting with platelet glycoprotein Ib. (1986) (249)
- Multimeric composition of factor VIII/von Willebrand factor following administration of DDAVP: implications for pathophysiology and therapy of von Willebrand's disease subtypes (1982) (247)
- A major factor VIII binding domain resides within the amino-terminal 272 amino acid residues of von Willebrand factor. (1987) (243)
- Protein C, an antithrombotic protein, is reduced in hospitalized patients with intravascular coagulation. (1982) (216)
- Subunit composition of plasma von Willebrand factor. Cleavage is present in normal individuals, increased in IIA and IIB von Willebrand disease, but minimal in variants with aberrant structure of individual oligomers (types IIC, IID, and IIE). (1986) (215)
- Structure of the von Willebrand factor domain interacting with glycoprotein Ib. (1988) (205)
- Determination of the von Willebrand's disease antigen (factor VIII-related antigen) in plasma by quantitative immunoelectrophoresis. (1975) (201)
- Synthetic factor VIII peptides with amino acid sequences contained within the C2 domain of factor VIII inhibit factor VIII binding to phosphatidylserine. (1990) (185)
- Effects of monoclonal antibodies against the platelet glycoprotein IIb/IIIa complex on thrombosis and hemostasis in the baboon. (1988) (182)
- Factor VIII/von Willebrand factor in subendothelium mediates platelet adhesion. (1985) (177)
- von Willebrand factor interaction with the glycoprotein IIb/IIa complex. Its role in platelet function as demonstrated in patients with congenital afibrinogenemia. (1986) (176)
- Detection of carriers of classic hemophilia using an immunologic assay for antihemophilic factor (factor 8(). (1971) (169)
- FVIII inhibitor IgG subclass and FVIII polypeptide specificity determined by immunoblotting. (1987) (165)
- Leukocyte procoagulant activity: enhancement of production in vitro by IgG and antigen-antibody complexes. (1977) (164)
- A heparin-binding domain of human von Willebrand factor. Characterization and localization to a tryptic fragment extending from amino acid residue Val-449 to Lys-728. (1987) (162)
- Characterization of the human factor VIII procoagulant protein with a heterologous precipitating antibody. (1982) (159)
- Active release of human platelet factor VIII-related antigen by adenosine diphosphate, collagen, and thrombin. (1978) (157)
- Molecular cloning of cDNA for human von willebrand factor: Authentication by a new method (1985) (152)
- Localization of human factor FVIII inhibitor epitopes to two polypeptide fragments. (1985) (151)
- Isolation of the von Willebrand factor domain interacting with platelet glycoprotein Ib, heparin, and collagen and characterization of its three distinct functional sites. (1989) (146)
- Aberrant multimeric structure of von Willebrand factor in a new variant of von Willebrand's disease (type IIC). (1982) (136)
- Multimeric structure of factor VIII/von Willebrand factor in von Willebrand's disease. (1980) (131)
- von Willebrand disease "Vicenza" with larger-than-normal (supranormal) von Willebrand factor multimers. (1988) (119)
- An immunogenic region within residues Val1670-Glu1684 of the factor VIII light chain induces antibodies which inhibit binding of factor VIII to von Willebrand factor. (1988) (117)
- Subunit composition of plasma von Willebrand factor in patients with the myeloproliferative syndrome. (1986) (116)
- Thrombin proteolysis of purified factor viii procoagulant protein: correlation of activation with generation of a specific polypeptide. (1983) (115)
- Ultrastructural localization of human platelet thrombospondin, fibrinogen, fibronectin, and von Willebrand factor in frozen thin section. (1985) (113)
- von Willebrand's disease antigen II. A new plasma and platelet antigen deficient in severe von Willebrand's disease. (1978) (112)
- Multimeric structure of platelet factor VIII/von Willebrand factor: the presence of larger multimers and their reassociation with thrombin-stimulated platelets. (1982) (110)
- Interaction of purified type IIB von Willebrand factor with the platelet membrane glycoprotein Ib induces fibrinogen binding to the glycoprotein IIb/IIIa complex and initiates aggregation. (1985) (105)
- Inhibition of platelet function with synthetic peptides designed to be high-affinity antagonists of fibrinogen binding to platelets. (1986) (104)
- Isolation and characterization of a collagen binding domain in human von Willebrand factor. (1986) (98)
- Independent modulation of von Willebrand factor and fibrinogen binding to the platelet membrane glycoprotein IIb/IIIa complex as demonstrated by monoclonal antibody. (1985) (96)
- BLOOD COAGULATION INITIATION BY A COMPLEMENT-MEDIATED PATHWAY (1971) (95)
- FACTOR VIII COAGULANT ACTIVITY AND FACTOR VIII-LIKE ANTIGEN: INDEPENDENT MOLECULAR ENTITIES (1973) (91)
- Factor-VIII-related antigen: multiple molecular forms in human plasma. (1975) (89)
- Increased von Willebrand factor antigen in the plasma of patients with vasculitis. (1984) (88)
- Immunofluorescent localization of adhesive glycoproteins in resting and thrombin-stimulated platelets. (1984) (86)
- Localization of the binding regions of a murine monoclonal anti-factor VIII antibody and a human anti-factor VIII alloantibody, both of which inhibit factor VIII procoagulant activity, to amino acid residues threonine351-serine365 of the factor VIII heavy chain. (1988) (83)
- Hereditary deficiency of the seventh component of complement. (1975) (83)
- Epitope mapping of the von Willebrand factor subunit distinguishes fragments present in normal and type IIA von Willebrand disease from those generated by plasmin. (1987) (80)
- Increased production and expression of tissue thromboplastin-like procoagulant activity in vitro by allogeneically stimulated human leukocytes. (1978) (80)
- Carbohydrate moiety of von Willebrand factor is not necessary for maintaining multimeric structure and ristocetin cofactor activity but protects from proteolytic degradation. (1984) (77)
- Von Willebrand's disease. (1976) (70)
- Studies of leukocyte kinetics in chronic lymphocytic leukemia. (1968) (68)
- A BLOOD COAGULATION ABNORMALITY IN RABBITS DEFICIENT IN THE SIXTH COMPONENT OF COMPLEMENT (C6) AND ITS CORRECTION BY PURIFIED C6 (1971) (68)
- Onset of manifestations of hepatic porphyria in relation to the influence of female sex hormones. (1966) (67)
- High-resolution analysis of von Willebrand factor multimeric composition defines a new variant of type I von Willebrand disease with aberrant structure but presence of all size multimers (type IC). (1985) (62)
- Type IIB von Willebrand's disease: differential clearance of endogenous versus transfused large multimer von willebrand factor. (1982) (62)
- Elevation of von Willebrand factor is independent of erythrocyte sedimentation rate and persists after glucocorticoid treatment in giant cell arteritis. (1984) (61)
- Blood coagulation and the inflammatory response. (1977) (61)
- Hybridoma antibodies to human von Willebrand factor (1984) (60)
- Type IIB Tampa: a variant of von Willebrand disease with chronic thrombocytopenia, circulating platelet aggregates, and spontaneous platelet aggregation (1985) (57)
- URINARY ALKALINE PHOSPHATASE ACTIVITY. I. ELEVATED URINARY LDH AND ALKALINE PHOSPHATASE ACTIVITIES FOR THE DIAGNOSIS OF RENAL ADENOCARCINOMAS. (1963) (56)
- Selective Absence of Large Forms of Factor VIII/Von Willebrand Factor in Acouired Von Willebrano’s Syndrome. Response to Transfusion (1979) (56)
- Human platelet-initiated formation and uptake of the C5-9 complex of human complement. (1976) (53)
- Human factor VIII procoagulant protein. Monoclonal antibodies define precursor-product relationships and functional epitopes. (1985) (51)
- The von willebrand factor domain-mediating botrocetin-induced binding to glycoprotein IB lies between Val449 and Lys728. (1987) (50)
- Platelets and von Willebrand disease. (1985) (50)
- Heparin-associated thrombocytopenia: observations on the mechanism of platelet aggregation. (1989) (49)
- The factor VIII abnormality in severe von Willebrand's disease. (1979) (48)
- A co-operative study for the detection of the carrier state of classic hemophilia. (1977) (47)
- Measurements of Platelet Function (1984) (46)
- A new variant of type II von Willebrand disease with aberrant multimeric structure of plasma but not platelet von Willebrand factor (type IIF). (1986) (43)
- Platelet factor VIII-related antigen: immunofluorescent localization. (1978) (43)
- Pneumococcus-induced serotonin release from human platelets. Identification of the participating plasma/serum factor as immunoglobulin. (1975) (41)
- FDA REPORT ON ENOVID. AD HOC ADVISORY COMMITTEE FOR THE EVALUATION OF A POSSIBLE ETIOLOGIC RELATION WITH THROMBOEMBOLIC CONDITIONS. (1963) (38)
- von Willebrand disease. (1987) (37)
- Type IIB Tampa: a variant of von Willebrand disease with chronic thrombocytopenia, circulating platelet aggregates, and spontaneous platelet aggregation. (1985) (37)
- Acquired von Willebrand's disease. Evidence for a quantitative and qualitative factor VIII disorder. (1978) (35)
- The effect of etiocholanolone on the entry of granulocytes into the peripheral blood. (1968) (29)
- Classification of von willebrand disease (1987) (28)
- Evidence that calpains and elastase do not produce the von Willebrand factor fragments present in normal plasma and IIA von Willebrand disease. (1988) (27)
- Further characterization of platelet-type von Willebrand's disease in Japan (1984) (26)
- Purification of factor VIII by monoclonal antibody affinity chromatography. (1988) (25)
- Proteolysis of von Willebrand factor after thrombolytic therapy in patients with acute myocardial infarction (1992) (23)
- Factor VIII structure and function. (1989) (23)
- Localization of the binding site for a factor VIII activity neutralizing antibody to amino acid residues Asp1663-Ser1669. (1988) (23)
- A Synthetic Factor VIII Peptide of Eight Amino Acid Residues (1677-1684) Contains the Binding Region of an Anti-Factor VIII Antibody which Inhibits the Binding of Factor VIII to von Willebrand Factor (1990) (21)
- Carbohydrate of the factor VIII/von Willebrand factor in von Willebrand's disease. (1979) (20)
- Interaction of factor VIII antigen in hemophilic plasmas with human antibodies to factor VIII. (1977) (20)
- Fine Mapping of Monoclonal Antibody Epitopes on Human von Willebrand Factor Using a Recombinant Peptide Library (1992) (19)
- Type II H von willebrand disease: New structural abnormality of plasma and platelet von willebrand factor in a patient with prolonged bleeding time and borderline levels of ristocetin cofactor activity (1989) (18)
- Pulmonary embolism and unexpected death in supposedly normal persons. A second look. (1970) (18)
- The effect of ellagic acid on delayed hypersensitivity reactions in guinea pigs. (1971) (18)
- von Willebrand's Disease. (1983) (18)
- Correlation of granulocyte mobilization with etiocholanolone and the subsequent development of myelosuppression in patients with acute leukemia receiving therapy. (1968) (17)
- Serum Lactate Dehydrogenase Elevation in Ambulatory Cardiac Patients: Evidence for Chronic Hemolysis (1967) (16)
- Physiology of the granulocyte. 2. (1968) (16)
- VON WILLEBRAND FACTOR, NOW CLONED (1986) (16)
- Further characterization of platelet-type von Willebrand's disease in Japan. (1984) (16)
- A murine monoclonal anti-factor VIII inhibitory antibody and two human factor VIII inhibitors bind to different areas within a twenty amino acid segment of the acidic region of factor VIII heavy chain. (1990) (14)
- Increases of leukocyte tissue factor activity stimulated by red cells sensitized with human blood group alloantibodies. (1982) (14)
- Factor VIII In Vessel Wall Influences Platelet Interaction With Subendothelium (1981) (13)
- ENHANCEMENT OF PRODUCTION IN VITRO BY IgG AND ANTIGEN-ANTIBODY COMPLEXES (1977) (12)
- von Willebrand factor binding to platelet glycoprotein Ib complex. (1992) (12)
- Isoelectric focusing of human von Willebrand factor in urea-agarose gels (1983) (12)
- Isoelectric focusing of human von Willebrand factor in urea-agarose gels. (1983) (11)
- CLASSIFICATION OF VARIANT von WILLEBRAND'S DISEASE SUBTYPES BY ANALYSIS OF FUNCTIONAL CHARACTERISTICS AND MULTIMERIC COMPOSITION OF FACTOR VIII/von WILLEBRAND FACTOR * (1981) (11)
- Physiology of the Granulocyte—Part 1 (1968) (11)
- A Blood Coagulation Abnormality in C6 Deficient Rabbits and Its Correction by Purified C6 (1971) (9)
- Peripheral leukocyte kinetic studies of acute leukemia in relapse and remission and chronic myelocytic leukemia in blastic crisis. (1968) (9)
- Factor VIII procoagulant protein. (1985) (9)
- von Willebrand factor multimers von Willebrand disease "Vicenza" with larger-than-normal (supranormal) (2011) (8)
- Physiology of the Granulocyte—Part 2 (1968) (7)
- Synthetic peptides inhibit the interaction of von Willebrand factor-platelet membrane glycoproteins (1993) (7)
- Spontaneous platelet aggregation in type IIB tampa von willebrand disease is inhibited by the 52/48‐kDa fragment of normal von willebrand factor, which contains the GPIb binding domain (1989) (6)
- Molecular immunology of factor VIII. (1974) (6)
- Partial Thromboplastin Time Reagents: Another Look (1985) (6)
- Complement-Induced Platelet Protein Alterations (1973) (5)
- Case report: 1‐deamino‐8‐D‐arginine vasopressin and cryoprecipitate in variant von Willebrand disease (1985) (5)
- Multiple Molecular Forms of Factor VIII Antigen in Normal Individuals and Von Willebrand’s Disease Patients (1977) (5)
- Physiology of the granulocyte. I. (1968) (5)
- Factor VIII/von Willebrand factor (1987) (4)
- [21] Secretion of von Willebrand factor from platelets (1989) (4)
- Molecular Biology of Factor VIII/von Willebrand Factor (1978) (4)
- Hemophilia, (Factor VIII deficiency) hematuria and urological intervention. (1970) (4)
- Human blood platelet factor VIII-related antigen: Demonstration of release by α-chymotrypsin (1979) (4)
- Mono clonal antibodies specific for factor viii from cellular hybrids (1980) (4)
- Factor VIII Structure and Function: Progress and Problems (1979) (3)
- Structure-function relationships of platelet glycoprotein Ib as a receptor for von Willebrand factor. (1986) (2)
- Apparent molecular weight of purified human factor VIII procoagulant protein compared with purified and plasma factor VIII procoagulant protein antigen. (1983) (2)
- Structure and function of factor VIII procoagulant protein. (1984) (2)
- The Platelet in C-Blood Coagulation Interaction (1973) (2)
- Heterogeneity in von Willebrand's disease. (1981) (2)
- Secretion of von Willebrand factor from platelets. (1989) (2)
- Factor VIII/von Willebrand factor. Structure and function. (1987) (1)
- The remission and relapse status of acute leukemia as studied by the in vitro uptake of tritiated thymidine by peripheral blood leukocytes. (1968) (1)
- Reduced Polymerization of Factor VIII/Von Willebrano Factor in Variants of Willebrand’s Disease (1979) (1)
- Human blood platelet factor VIII-related antigen : demonstration of release by alpha-chymotrypsin. (1979) (1)
- [Multimeric structure of factor VIII/von Willebrand factor released from human platelets by ADP, collagen and thrombin]. (1983) (1)
- factor fragments present in normal plasma and IIA von Willebrand disease Evidence that calpains and elastase do not produce the von Willebrand (2011) (1)
- A NEW PLASMA AND PLATELET ANTIGEN DEFICIENT IN SEVERE VON WILLEBRAND'S DISEASE (1)
- Heterogeneity of type IIA von Willebrand Disease: Studies with protease inhibitor (1986) (1)
- von Willebrand ' s Disease Antigen II A NEWPLASMA ANDPLATELET ANTIGEN DEFICIENT IN SEVERE VONWILLEBRAND ' S DISEASE (0)
- thrombin-induced factor VIII activation in humans (2017) (0)
- Viii:c preparation (1996) (0)
- TREATMENT OFFACTOR VIII INHIBITORS 75 Inventors : (2017) (0)
- von Willebrand Disease "Vicenza" With Larger-Than-Normal (Supranormal) von (2016) (0)
- Factor viii:c preparation (1994) (0)
- Factor VIII: C coagulation agent, process for their preparation and process for its extraction (1984) (0)
- Peptides of the units derived from von Willebrand factor by the factor VIII binding domain (1988) (0)
- Nya koagulantpolypeptider of the factor of iii. (1985) (0)
- Improved immune adsorbent (1991) (0)
- Ultra purification of factor VIII. (1982) (0)
- Peptide used for purification of factor viii (1988) (0)
- Factor VIII polypeptidkoaguleringsmiddel and monoclonal antibodies to these (1984) (0)
- Ultrapurification de facteur viii (1982) (0)
- Monoclonal antibodies against novel Factor VIII Gerinnungspolypeptide (1984) (0)
- 1-Deamino-8-D-arginine vasopressin and cryoprecipitate in variant von Willebrand disease. (1985) (0)
- Selective Binding of Different Molecular Species of Factor VIII to Isolated Human Platelet Membranes and to Intact Thrombin Stimulated Platelet (1979) (0)
- [Further evaluation of GPIb binding domain of vWf by synthetic peptides]. (1992) (0)
- Seventh Component of Complement (1975) (0)
- Human Blood Platelet Factor VIII-Related Antigen: A Glycocalicin-Like Protein (1977) (0)
- A plasmin-like, neutral, calcium dependent protease is responsible for the loss of the high molecular weight (HMW) multimers in the carbohydrate (CHO) modified von Willebrand factor (VWF) (1986) (0)
- Monoclonal antibodies to the new factor VIII koaguleringspolypeptider (1997) (0)
- Foerfarande Foer Treatment of Faktor VIII-inhibitorer. (1988) (0)
- UNITED STATES PATENT AND TRADEMARK OFFICE CERTIFICATE OF CORRECTION Bll 4 , 683 , 291 July 3 , 1990 (2017) (0)
- Peptides that inhibit von Willebrand Factor binding to the platelet SPIB receptor (1994) (0)
- Factor-VIII/von Willebrand factor (2018) (0)
- Factor VIII/Von Willebrand factor (2015) (0)
- patients with acute myocardial infarction Proteolysis of von Willebrand factor after thrombolytic therapy in (2011) (0)
- vWAgII: A New von Willebrand’s Disease Antigen (1977) (0)
- Monoclonal antibody specific to factor viii:c clotting factor peptides (1993) (0)
- glycoprotein IB lies between Val449 and Lys728 The von willebrand factor domain-mediating botrocetin-induced binding to (2013) (0)
- Peptides that inhibit binding of von Willebrand factor. (1987) (0)
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What Schools Are Affiliated With Theodore S. Zimmerman?
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