| G |
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G12/13 Pathways Potentiate Akt Phosphorylation Mediated by Gi/Gz Pathways in Platelets
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| Kim S, Jin J, Kunapuli SP |
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Gait Alterations Exist in Children with Haemophilia after Relatively Few Haemarthroses and Despite Prophylaxis – A 3D Motion Analysis Study
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| Stephensen D, Drechsler WI, Winter M, Evans G, Scott OM |
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Galactosylation of GPIba by an Externally Active Endogenous b4Galactosyl Trasferase Prolongs Platelet Survival
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| Hoffmeister KM |
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Gender Related Differences in Coagulation Activity in Unstable Coronary Artery Disease Patients and Apparently Healthy Individuals
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| Oldgren J, Johnston N, Wallentin L, Siegbahn A |
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Gene Conversions Are a Common Cause of von Willebrand Disease
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| Gupta PK, Adamtziki E, Budde U, Harbeck-Seu A, Kannan M, Jaiprakash M, Oyen F, Obser T, Wedekind I, Saxena R, Schneppenheim R |
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Gene Expression Abnormalities in Aspirin Hyper-responders
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| Ferraris VA, Ferraris SP, Camp P, Settles J, Fisher R |
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Gene Expression Comparison Between Monocytes in Culture and Atherosclerotic Laser Microdissected Resident Macrophages
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| Collot-Teixeira S, Bultelle F, Martin J, Clutterbuck R, Poston R, McGregor JL |
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Gene Expression Profiling in Antiphospholipid Syndrome Reveals Distinct Molecular Signatures with Diagnostic Value
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| Potti A, Bild A, Mette C, Britt M, Dressman H, Nevins J, Ortel TL |
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Gene Mutation and ITT Response in the Italian Cohort of Patients with Haemophilia A
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| Salviato R, Belvini D, Radossi P, Zanon E, Castaman G, Gandini G, Tagariello G |
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Gene Polymorphisms of Hemostasis And Lipid Metabolism in Apparently Healthy Individuals from Southwest Germany
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| Haubelt H, Landmann T, Preiss A, Bach J, Hellstern P |
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Gene Structures of Two Functionally Diverse Prothrombin Activators, Trocarin D and Coagulation Factor X, in Tropidechis Carinatus Snake
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| Reza MA, Swarup S, Kini RM |
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Gene Targeting or Pharmacological Inhibition of Rac GTPases Prolongs the Bleeding Time and Reduces Platelet Adhesion, Secretion and Aggregation: Evidence for the Rac-Mediated Activation of MAP Kinases during Platelet Activation
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| Akbar H, Wang L, Chen L, Johnson J, Williams DA, Zheng Y |
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Gene Transfer for Hemophilia: can Therapeutic Efficacy in Large Animals be Safely Translated to Patients?
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| High Katherine |
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General Properties of the Coagulation System and Determination of Kinetic Constants for Biochemical Reactions
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| Tyurin KV, Khanin MA |
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Generation and Characterization of ADAMTS13-Deficient Mice
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| Banno F, Kokame K, Okuda T, Honda S, Miyata S, Kato H, Tomiyama Y, Miyata T |
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Generation of Activated Protein C and Phagocyte Activation Associated with Immmunosuppression Using Anti-Thymocyte Globulin for Kidney Transplantation
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| Fernández JA, Griffin JH, Turunen AJ, Petäjä J, Lindgren L, Salmela KT, Kyllönen LE, Mäkisalo H, Siitonen SM, Pesonen EJ |
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Generation of Kininogen Deficient Mice
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| Merkulov SM, Lu X, Barnes E, Luo G, McCrae KR |
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Genetic Analysis of Chinese Patients with Inherited Afibrinogenemia
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| Fang Y, Wang XF, Wang HL, Fu QH, Wu WM, Ding QL, Dai J, Hu YQ, Wang ZY |
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Genetic and Acquired Risk Factors in Patients with Portal and Mesenteric Venous Thrombosis
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| Macarone Palmieri N, Tufano A, Coppola A, Cirillo F, Lombardini D, Meola M, Cerbone AM, Di Minno G |
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Genetic and Environmental Regulation of Factor VII Levels: Results from the IMMIDIET Project
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| Di Castelnuovo A, Zito F, de Gaetano G, Arnout J, Cappuccio FP, van Dongen MC, de Lorgeril M, Dirckx C, Donati MB, Sieri S, Siani A, Iacoviello L |
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Genetic and Phenotypic Analysis of Families with Inherited Hypo- and Dys-fibrinogenemia
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| Batorova A, Horvathova D, Lazur J, Mistrik M, de Moerloose P, Neerman-Arbez M |
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Genetic Defects of von Willebrand Factor as a Determinant of Its Survival in the Circulation
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| Denis CV, Meyer D, Lenting PJ |
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Genetic Evidence that CD154 (CD40 Ligand) Plays a Pathophysiologic Role in the Systemic Coagulopathy Associated with Murine Models of Experimental Metastasis and Endotoxemia
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| Ingersoll SB, Amirkhosravi A, Langer F, Walker J, Meyer T, Amaya M, Francis JL |
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Genetic Frequencies of Single Nucleotide Polymorphisms in Predisposition to a Hypercoagulable State in Taiwan
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| Lin JS, Shen MC, Lin CY, Yu YY, Yeh IM, Li SY |
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Genetic Manipulation of Megakaryocytes to Study Platelet Integrin Regulation
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| Parise LV, Yuan W, McFadden AW, Wang ZY, Larson MK, Leisner TM, DeNofrio JC, Liu J, Clark S |
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Genetic Polymorphisms and Environmental Influences in Arterial Occlusive Diseases
|
| Shmeleva V, Kapustin S |
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Genetic Study of 16 Women with Decreased FVIII Level and Assessment of Haemophilia a Carrier Status
|
| Vinciguerra C, Meunier S, Pernod G, Polack B, Trzeciak MC, Negrier C |
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Genetic Study of von Willebrand Factor in Twenty-two Members of an Argentinian Family
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| Carballo GA, Woods AI, Vera E, Casais P, Aletti G, Farías C, Kempfer AC, Lazzari MA |
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Genetic variants in COX 1-, GP Ia/IIb- and FXIIIa-subunits: Effects on Response to Aspirin in Patients with Peripheral Arterial Occlusive Disease
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| Mani H, Geisen C, Ivaskevicius V, Watzka M, Oldenburg J, Lindhoff-Last E |
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Genetic Variation in ADP-receptor P2Y12 is Associated with the Stability of Platelet Aggregates in Healthy Subjects
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| Rude[zcaron] G, de Bruijne ELE, de Maat MPM, Leebeek FWG |
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Genetic Variation of VWD Type I in Sweden: Tracing the Evolutionary History of the von Willebrand Factor Gene Region
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| Johansson AM, Säll T, Lethagen S, Hall L, Halldén C |
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Genetic Variation within the Interleukin 6 Promoter Determines Interleukin 6 Expression Levels in Atherosclerosis
|
| Khwaja H, Beeton L, Green FR |
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Genotype Associations with Dyslipoproteinemia in Male Venous Thrombosis Patients
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| Pecheniuk NM, Deguchi H, Averell PM, Elias DJ, Griffin JH |
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Genotyping of Hemophilia B in Iran by SSCP and Sequencing
|
| M Karimipoor, S Zeinali, N Nafissi, M Lak, R Safaee |
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Giant Cells Thrombocytopenia MYH9-Related, Management of Mild/Moderate Bleeding Episodes
|
| Corinaldesi G, Corinaldesi C |
| |
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Glucose Uptake Via GLUT3 in Human Platelets Is Regulated Via PKB
|
| Andrade Ferreira I, Mocking AIM, Varlack S, Wnuk M, Akkerman JWN |
| |
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Glucosylceramide Synthase, Glucosylceramide Plasma-Based Assay and Prothrombotic Conditions
|
| Faioni EM, Fontana G, Carpani G, Biguzzi E, Biondi ML, Cattaneo M |
| |
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Glycation Induces Formation of Cross-b Structure and Activation of Tissue-Type Plasminogen Activator (tPA) and Factor XII
|
| Bouma B, Kroon-Batenburg LMJ, Wu Y-P, de Groot Ph.G., Gebbink MFBG |
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Glycoprotein (GP) VI Is Associated with GP-Ib-IX-V on the Membrane of Resting and Activated Platelets
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| Arthur J, Gardiner E, Wijeyewickrema L, Ozaki Y, Kahn M, Andrews R, Berndt M |
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Glycoprotein Iba-Mediated Platelet Adhesion and Aggregation to Immobilized Thrombin under Conditions of Flow
|
| Weeterings C, Adelmeijer J, Myles T, de Groot PG, Lisman T |
| |
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Glycoprotein Ib-IX-V Complex Mediates Localization of Alpha-thrombin to Lipid Rafts on the Platelet Membrane
|
| Baglia FA, Walsh PN |
| |
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Glycoprotein IIb/IIIa Blockade Inhibits Platelet Phosphatidylserine Exposure But Not Vesiculation
|
| Razmara M, Hu H, Li N |
| |
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Glycoprotein VI Structure-Function Relationship: Identification of Collagen Binding Domains Using GPVI/FcaR Chimera
|
| Minullina I, Dumont B, Lacapère JJ, Monteiro R, Arocas V, Jandrot-Perrus M |
| |
|
Glycosylation Site Analysis of Human Platelet Proteins
|
| Lewandrowski U, Moebius J, Walter U, Sickmann A |
| |
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Glykoprotein VI Mediates Platelet Adhesion to Vulnerable Human Atherosclerotic Plaque
|
| Schulz C, Penz S, Hoffmann C, Schneider S, Siess W, Gawaz M, Massberg S |
| |
|
GPVI Deficiency Associated with Unexpected Severe Bleeding in a 33 year Old Patient with Moderate Thrombocytopenia and Autoantibodies Against the Ig-like Domains
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| Smethurst PA, Garner SF, Davies LW, Rankin A, Campbell K, Farndale RW, Tillyer ML, Ouwehand WH |
| |
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GPVI-Deficient Mice Lack Collagen Responses and are Protected Against Experimentally-Induced Pulmonary Thromboembolism
|
| Lockyer S, Okuyama K, Begum S, Le S, Sun B, Matsumoto Y, Yoshitake M, Kambayashi JI, Tandon NN |
| |
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GPVI-Dependent Binding of Murine Platelets to a Series of Triple-Helical Peptides Derived from Human Type III Collagen
|
| Jarvis GE, Raynal N, Peachey AR, Slatter D, Farndale RW |
| |
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Gynaecological Problems in Severe Congenital Factor VII Deficiency
|
| Batorova A, Jankovicova D, Mistrik M, Cupanik V, Herrmann FH |
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