antithrombin : Related Words Words similar in meaning to antithrombin
- molecule«
- heparin«
- enzyme«
- reactive site loop«
- coagulation«
- β-antithrombin«
- antithrombic«
- α-antithrombin«
- thrombin«
- latent antithrombin«
- antithrombin deficiency«
- xa inhibition«
- heparin affinity«
- factor ixa«
- thrombin inhibition«
- at iii«
- figure«
- mutation«
- type ii pe«
- type ii antithrombin deficiency«
- native antithrombin«
- antithrombin gene«
- amino acid«
- human antithrombin«
- antithrombin activity«
- conformational change«
- angiogenesis«
- antithrombin iii«
- standardization committee«
- latent form«
- hinge region«
- haemostasis«
- glycosylation site«
- protein«
- type«
- recombinant antithrombins«
- p15 amino acid«
- p14 p15 reactive site loop«
- initial heparin«
- inactive antithrombin«
- decreased thrombin inactivation«
- antithrombin structure«
- antithrombin iv«
- reactive bond«
- minor insertion«
- latent conformation«
- deficiency«
- subgroup iia«
- pentasaccharide«
- mechanism result«
- codon«
- thrombosis«
- β-turn«
- protease complex«
- protease«
- allosteric«
- factor ii«
- neutrophil elastase«
- conformational flexibility«
- serpins«
- revised system«
- reactive site«
- protease enzyme«
- blood«
- protease activity«
- minor form«
- dimerisation«
- deletion«
- plasma«
- scientific«
- international society«
- main body«
- blood coagulation«
- model b«
- fibrinogen«
- heterodimer«
- at«
- affinity«
- structure«
- tumor growth«
- blood plasma«
- arginine«
- genetic mutation«
- sepsis«
- result«
- presence«
- classification«
- conformation«
- cleavage«
- form«
- mechanism«
- complex«
- inhibitor«
- variable glycosylation pattern«
- unstable antithrombins«
- type ii hbs.«
- type ii hb«
- type ii antithrombin«
- total antithrombin«
- thrombogenic event«
- thrombin protease«
- thrombin inactivation«
- target coagulation protease«
- subsequent functional analysis«
- subsequent dimer formation«
- subgroup iic«
- subgroup iib«
- subgroup ib individual«
- subgroup ia individual«
- specific reactive peptide bond«
- specific antithrombin genetic mutation«
- specie additional«
- severe injury trauma«
- role antithrombin«
- reduced antithrombin activity«
- reactive site result«
- rapid proteolytic cleavage«
- proteinuria nephrotic syndrome«
- protease inactivation result«
- premature generation«
- prelatent form«
- prelatent antithrombin«
- pleiotrophic effect«
- plasma protease inhibitor«
- plasma coagulation inhibitor subcommittee«
- physiological target protease«
- physiological target enzyme«
- p15 gly«
- normal thrombin inactivation«
- normal protease substrate result«
- normal physiological condition angiogenesis«
- normal human antithrombin«
- normal heparin affinity«
- normal functional level«
- normal factor xa inactivation«
- normal codon«
- normal antithrombin level«
- normal antithrombin concentration«
- normal antithrombin«
- native molecule inactivation«
- mouse antithrombins«
- modern mutational characterisation«
- modern characterisation technique investigator«
- minimal heparin pentasaccharide sequence«
- minimal heparin«
- mechanism stimulation«
- mechanism heparin stimulation«
- maximal rate constant«
- length heparin«
- latent antithrombin formation«
- individual antithrombin toponym«
- inactive antithrombins«
- immunochemical antithrombin analysis«
- immature liver secondary«
- iii bind«
- hinge region conformational change«
- heparin cofactor ii.«
- heparin chain adjacent«
- heparin binding result«
- functional antithrombin level«
- fold enhancement«
- factor xa inactivation«
- factor ixa inhibition«
- extra sixth strand«
- equimolar complex«
- enzyme c1«
- effective inhibition«
- designation antithrombin«
- cys8-cys128«
- cys248-cys430«
- cys21-cys95«
- completion biosynthesis«
- cga→tga«
- c1s subunit«
- bond p3-p4«
- blood coagulation protease«
- birth.liver dysfunction«
- beta sheet a.«
- beta sheet a«
- bacterial enzyme thermolysin«
- at iv«
- at ii«
- asn-135«
- antithrombin reactive bond«
- antithrombin nomenclature«
- antithrombin mutational database«
- antithrombin mutation«
- antithrombin inactive«
- antithrombin ii«
- antithrombin heparin«
- antithrombin functional activity«
- antithrombin conformation«
- antithrombin concentration«
- antithrombin blood concentration«
- antihrombin«
- antiangiogenic antithrombin«
- angiogenic stimulatory factor«
- angiogenic stimulators«
- angiogenic inhibitory factor tumor cell«
- amino acid p14«
- allosteric activation«
- active native antithrombin molecule«
- acquired antithrombin deficiency«
- -tours«
- -paris-2«
- -paris-1«
- -padua-2«
- -barcelona«
- -amien«
- -alger«
- binding«
- inhibition«
- thrombin complex«
- specific pentasaccharide sulfation sequence«
- single glycosylation site«
- pentasaccharide sequence«
- normal blood coagulation«
- ment.«
- hereditary antithrombin deficiency«
- heparin polymer«
- glcns(3s,6s)-idoa(2s)-glcns(6s«
- glcnac/ns(6s)-glca«
- cdna sequencing«
- antithrombin molecule«
- anticoagulant drug heparin«
- additional glycosylation«
- consequence«
- recurrent venous thrombosis«
- factor xa inhibition«
- diffuse intravascular coagulation«
- subgroup«
- rate«
- type ii deficiency«
- thrombin activity«
- potential glycosylation site«
- normal affinity«
- angiogenic inhibitor«
- alpha 2-antiplasmin«
- frame shift mutation«
- extra amino acid«
- atryn«
- alpha 1-antichymotrypsin«
- additional binding«
- xiia«
- reduced affinity«
- proteolytic process«
- fold lower«
- usual substrate«
- thrombotic disease«
- contact activation pathway«
- cleaved«
- similar amino acid«
- rate enhancement«
- heparin cofactor ii«
- tissue factor pathway«
- type iic«
- extreme heating«
- fold«
- formation«
- plasminogen activator inhibitor-1«
- extended conformation«
- rabbit«
- toponyms«
- potential n«
- glycosylation pattern«
- physiological impact«
- monomeric unit«
- intramolecular disulfide bond«
- factor x.«
- similar bond«
- increased flexibility«
- experimental animal model«
- % amino acid sequence identity«
- sustained production«
- viia«
- factor xii«
- factor xi«
- cow«
- protein therapeutic«
- termination codon«
- thermodynamic control«
- pai-1«
- extrinsic pathway«
- classical complement pathway«
- human blood plasma«
- native conformation«
- intrinsic pathway«
- coagulation system«
- serpin«
- mammalian cell line«
- baculovirus«
- insect cell«
- individual suffering«
- physiological level«
- factor vii«
- amino acid position«
- mrna processing«
- point mutation«
- serine protease inhibitor«
- crystallographic structure«
- ixa«
- factor ix«
- distinct mechanism«
- sheep«
- factor xa«
- kallikrein«
- active conformation«
- type ib«
- type iib«
- ternary complex«
- premature termination«
- type iia«
- human plasma«
- tumor development«
- plasmin«
- factor x«
- cardiopulmonary bypass«
- coagulopathy«
- molar concentration«
- lesser scale«
- terminal portion«
- tissue injury«
- 3-dimensional structure«