JP2012220493A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2012220493A5 JP2012220493A5 JP2012080672A JP2012080672A JP2012220493A5 JP 2012220493 A5 JP2012220493 A5 JP 2012220493A5 JP 2012080672 A JP2012080672 A JP 2012080672A JP 2012080672 A JP2012080672 A JP 2012080672A JP 2012220493 A5 JP2012220493 A5 JP 2012220493A5
- Authority
- JP
- Japan
- Prior art keywords
- lyophilized product
- kit
- kit according
- platelet
- platelet function
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000004108 freeze drying Methods 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 239000012928 buffer substance Substances 0.000 claims description 5
- 208000010110 spontaneous platelet aggregation Diseases 0.000 claims description 5
- 239000003112 inhibitor Substances 0.000 claims description 4
- 239000004615 ingredient Substances 0.000 claims description 2
- 239000008280 blood Substances 0.000 claims 4
- 210000004369 blood Anatomy 0.000 claims 4
- 238000000034 method Methods 0.000 claims 3
- 238000002360 preparation method Methods 0.000 claims 3
- OHCQJHSOBUTRHG-KGGHGJDLSA-N FORSKOLIN Chemical compound O=C([C@@]12O)C[C@](C)(C=C)O[C@]1(C)[C@@H](OC(=O)C)[C@@H](O)[C@@H]1[C@]2(C)[C@@H](O)CCC1(C)C OHCQJHSOBUTRHG-KGGHGJDLSA-N 0.000 claims 2
- KWPACVJPAFGBEQ-IKGGRYGDSA-N (2s)-1-[(2r)-2-amino-3-phenylpropanoyl]-n-[(3s)-1-chloro-6-(diaminomethylideneamino)-2-oxohexan-3-yl]pyrrolidine-2-carboxamide Chemical compound C([C@@H](N)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)CCl)C1=CC=CC=C1 KWPACVJPAFGBEQ-IKGGRYGDSA-N 0.000 claims 1
- GMVPRGQOIOIIMI-UHFFFAOYSA-N (8R,11R,12R,13E,15S)-11,15-Dihydroxy-9-oxo-13-prostenoic acid Natural products CCCCCC(O)C=CC1C(O)CC(=O)C1CCCCCCC(O)=O GMVPRGQOIOIIMI-UHFFFAOYSA-N 0.000 claims 1
- IHPYMWDTONKSCO-UHFFFAOYSA-N 2,2'-piperazine-1,4-diylbisethanesulfonic acid Chemical compound OS(=O)(=O)CCN1CCN(CCS(O)(=O)=O)CC1 IHPYMWDTONKSCO-UHFFFAOYSA-N 0.000 claims 1
- DIOSHTLNZVXJOF-UHFFFAOYSA-N 2,5-bis(3-oxobutanoylamino)benzenesulfonic acid Chemical compound CC(=O)CC(=O)NC1=CC=C(NC(=O)CC(C)=O)C(S(O)(=O)=O)=C1 DIOSHTLNZVXJOF-UHFFFAOYSA-N 0.000 claims 1
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 claims 1
- BSYNRYMUTXBXSQ-FOQJRBATSA-N 59096-14-9 Chemical compound CC(=O)OC1=CC=CC=C1[14C](O)=O BSYNRYMUTXBXSQ-FOQJRBATSA-N 0.000 claims 1
- AEOBEOJCBAYXBA-UHFFFAOYSA-N A2P5P Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(O)=O)C(O)C1OP(O)(O)=O AEOBEOJCBAYXBA-UHFFFAOYSA-N 0.000 claims 1
- 239000008001 CAPS buffer Substances 0.000 claims 1
- 239000008000 CHES buffer Substances 0.000 claims 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims 1
- SUZLHDUTVMZSEV-UHFFFAOYSA-N Deoxycoleonol Natural products C12C(=O)CC(C)(C=C)OC2(C)C(OC(=O)C)C(O)C2C1(C)C(O)CCC2(C)C SUZLHDUTVMZSEV-UHFFFAOYSA-N 0.000 claims 1
- 108010056764 Eptifibatide Proteins 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 239000007995 HEPES buffer Substances 0.000 claims 1
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 claims 1
- 102000007625 Hirudins Human genes 0.000 claims 1
- 108010007267 Hirudins Proteins 0.000 claims 1
- 101000782195 Homo sapiens von Willebrand factor Proteins 0.000 claims 1
- 239000007993 MOPS buffer Substances 0.000 claims 1
- -1 MRS2279 Chemical compound 0.000 claims 1
- MKWKNSIESPFAQN-UHFFFAOYSA-N N-cyclohexyl-2-aminoethanesulfonic acid Chemical compound OS(=O)(=O)CCNC1CCCCC1 MKWKNSIESPFAQN-UHFFFAOYSA-N 0.000 claims 1
- 239000007990 PIPES buffer Substances 0.000 claims 1
- 239000007983 Tris buffer Substances 0.000 claims 1
- 208000034953 Twin anemia-polycythemia sequence Diseases 0.000 claims 1
- NMVWLEUONAKGCD-SMWKGLLFSA-N [(1r,2s,4s,5s)-4-[2-iodo-6-(methylamino)purin-9-yl]-2-phosphonooxy-1-bicyclo[3.1.0]hexanyl]methyl dihydrogen phosphate Chemical compound CNC1=NC(I)=NC2=C1N=CN2[C@@H]1[C@H]2C[C@@]2(COP(O)(O)=O)[C@@H](OP(O)(O)=O)C1 NMVWLEUONAKGCD-SMWKGLLFSA-N 0.000 claims 1
- AEOBEOJCBAYXBA-KQYNXXCUSA-N [(2r,3r,4r,5r)-2-(6-aminopurin-9-yl)-4-hydroxy-5-(phosphonooxymethyl)oxolan-3-yl] dihydrogen phosphate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1OP(O)(O)=O AEOBEOJCBAYXBA-KQYNXXCUSA-N 0.000 claims 1
- ZQXUQOHLHUWLSA-WOUKDFQISA-N [[[[(2r,3s,4r,5r)-5-(6-amino-2-propylsulfanylpurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]-difluoromethyl]phosphonic acid Chemical compound C12=NC(SCCC)=NC(N)=C2N=CN1[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)C(F)(F)P(O)(O)=O)[C@@H](O)[C@H]1O ZQXUQOHLHUWLSA-WOUKDFQISA-N 0.000 claims 1
- 229960000446 abciximab Drugs 0.000 claims 1
- WHTCPDAXWFLDIH-KQYNXXCUSA-N adenosine 3',5'-bismonophosphate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@H]1O WHTCPDAXWFLDIH-KQYNXXCUSA-N 0.000 claims 1
- 229960000711 alprostadil Drugs 0.000 claims 1
- 229940127218 antiplatelet drug Drugs 0.000 claims 1
- GAQWEBYIOMWWHZ-ZJWYQBPBSA-N azane;[(2r,3s,5r)-5-[6-(methylamino)purin-9-yl]-2-(phosphonooxymethyl)oxolan-3-yl] dihydrogen phosphate Chemical compound [NH4+].[NH4+].C1=NC=2C(NC)=NC=NC=2N1[C@H]1C[C@H](OP(O)([O-])=O)[C@@H](COP(O)([O-])=O)O1 GAQWEBYIOMWWHZ-ZJWYQBPBSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 229950000634 cicaprost Drugs 0.000 claims 1
- ARUGKOZUKWAXDS-SEWALLKFSA-N cicaprost Chemical compound C1\C(=C/COCC(O)=O)C[C@@H]2[C@@H](C#C[C@@H](O)[C@@H](C)CC#CCC)[C@H](O)C[C@@H]21 ARUGKOZUKWAXDS-SEWALLKFSA-N 0.000 claims 1
- 229960004588 cilostazol Drugs 0.000 claims 1
- RRGUKTPIGVIEKM-UHFFFAOYSA-N cilostazol Chemical compound C=1C=C2NC(=O)CCC2=CC=1OCCCCC1=NN=NN1C1CCCCC1 RRGUKTPIGVIEKM-UHFFFAOYSA-N 0.000 claims 1
- OHCQJHSOBUTRHG-UHFFFAOYSA-N colforsin Natural products OC12C(=O)CC(C)(C=C)OC1(C)C(OC(=O)C)C(O)C1C2(C)C(O)CCC1(C)C OHCQJHSOBUTRHG-UHFFFAOYSA-N 0.000 claims 1
- 229960002768 dipyridamole Drugs 0.000 claims 1
- IZEKFCXSFNUWAM-UHFFFAOYSA-N dipyridamole Chemical compound C=12N=C(N(CCO)CCO)N=C(N3CCCCC3)C2=NC(N(CCO)CCO)=NC=1N1CCCCC1 IZEKFCXSFNUWAM-UHFFFAOYSA-N 0.000 claims 1
- 150000002016 disaccharides Chemical class 0.000 claims 1
- 229960001123 epoprostenol Drugs 0.000 claims 1
- KAQKFAOMNZTLHT-VVUHWYTRSA-N epoprostenol Chemical compound O1C(=CCCCC(O)=O)C[C@@H]2[C@@H](/C=C/[C@@H](O)CCCCC)[C@H](O)C[C@@H]21 KAQKFAOMNZTLHT-VVUHWYTRSA-N 0.000 claims 1
- 229960004468 eptifibatide Drugs 0.000 claims 1
- GLGOPUHVAZCPRB-LROMGURASA-N eptifibatide Chemical compound N1C(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCCNC(=N)N)NC(=O)CCSSC[C@@H](C(N)=O)NC(=O)[C@@H]2CCCN2C(=O)[C@@H]1CC1=CN=C2[C]1C=CC=C2 GLGOPUHVAZCPRB-LROMGURASA-N 0.000 claims 1
- 229960002897 heparin Drugs 0.000 claims 1
- 229920000669 heparin Polymers 0.000 claims 1
- WQPDUTSPKFMPDP-OUMQNGNKSA-N hirudin Chemical compound C([C@@H](C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC=1C=CC(OS(O)(=O)=O)=CC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCCN)NC(=O)[C@H]1N(CCC1)C(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H]1NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(O)=O)NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@H](CC(C)C)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@@H]2CSSC[C@@H](C(=O)N[C@@H](CCC(O)=O)C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@H](C(=O)N[C@H](C(NCC(=O)N[C@@H](CCC(N)=O)C(=O)NCC(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)N2)=O)CSSC1)C(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H]1NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CC=2C=CC(O)=CC=2)NC(=O)[C@@H](NC(=O)[C@@H](N)C(C)C)C(C)C)[C@@H](C)O)CSSC1)C(C)C)[C@@H](C)O)[C@@H](C)O)C1=CC=CC=C1 WQPDUTSPKFMPDP-OUMQNGNKSA-N 0.000 claims 1
- 229940006607 hirudin Drugs 0.000 claims 1
- 229940034998 human von willebrand factor Drugs 0.000 claims 1
- 229960002240 iloprost Drugs 0.000 claims 1
- HIFJCPQKFCZDDL-ACWOEMLNSA-N iloprost Chemical compound C1\C(=C/CCCC(O)=O)C[C@@H]2[C@@H](/C=C/[C@@H](O)C(C)CC#CC)[C@H](O)C[C@@H]21 HIFJCPQKFCZDDL-ACWOEMLNSA-N 0.000 claims 1
- 230000005764 inhibitory process Effects 0.000 claims 1
- 239000000106 platelet aggregation inhibitor Substances 0.000 claims 1
- GMVPRGQOIOIIMI-DWKJAMRDSA-N prostaglandin E1 Chemical compound CCCCC[C@H](O)\C=C\[C@H]1[C@H](O)CC(=O)[C@@H]1CCCCCCC(O)=O GMVPRGQOIOIIMI-DWKJAMRDSA-N 0.000 claims 1
- XEYBRNLFEZDVAW-UHFFFAOYSA-N prostaglandin E2 Natural products CCCCCC(O)C=CC1C(O)CC(=O)C1CC=CCCCC(O)=O XEYBRNLFEZDVAW-UHFFFAOYSA-N 0.000 claims 1
- 229960003425 tirofiban Drugs 0.000 claims 1
- COKMIXFXJJXBQG-NRFANRHFSA-N tirofiban Chemical group C1=CC(C[C@H](NS(=O)(=O)CCCC)C(O)=O)=CC=C1OCCCCC1CCNCC1 COKMIXFXJJXBQG-NRFANRHFSA-N 0.000 claims 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 claims 1
- 238000000691 measurement method Methods 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11160934A EP2508892A1 (de) | 2011-04-04 | 2011-04-04 | Kontrollen und Kit für Thrombozytenaktivitätsteste |
| EP11160934.3 | 2011-04-04 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012220493A JP2012220493A (ja) | 2012-11-12 |
| JP2012220493A5 true JP2012220493A5 (enExample) | 2015-03-05 |
| JP5947085B2 JP5947085B2 (ja) | 2016-07-06 |
Family
ID=44123219
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012080672A Active JP5947085B2 (ja) | 2011-04-04 | 2012-03-30 | 血小板活性試験のための対照及びキット |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US8741873B2 (enExample) |
| EP (2) | EP2508892A1 (enExample) |
| JP (1) | JP5947085B2 (enExample) |
| ES (1) | ES2635196T3 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6012455B2 (ja) * | 2012-12-21 | 2016-10-25 | シーメンス ヘルスケア ダイアグノスティクス プロダクツ ゲゼルシヤフト ミツト ベシユレンクテル ハフツング | 血小板機能を測定するシステムにおいて測定結果を標準化する方法 |
| CN105652022B (zh) * | 2015-12-31 | 2017-10-10 | 浙江盛域医疗技术有限公司 | 血栓弹力图仪质控品及其制备方法 |
| US20190049428A1 (en) * | 2016-02-17 | 2019-02-14 | Sony Corporation | Platelet aggregability analyzing device, platelet aggregability analyzing system, platelet aggregability analyzing program, and method of analyzing platelet aggregability |
| JP7110360B2 (ja) | 2017-10-09 | 2022-08-01 | テルモ ビーシーティー バイオテクノロジーズ,エルエルシー | 凍結乾燥方法 |
| JP7230429B2 (ja) | 2018-10-25 | 2023-03-01 | ソニーグループ株式会社 | 血小板凝集能解析装置、血小板凝集能解析方法及び血小板凝集能解析システム |
| CN113597532B (zh) | 2019-03-14 | 2023-02-17 | 泰尔茂比司特生物技术有限公司 | 冻干容器填充固定装置、系统及使用方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4358394A (en) | 1979-05-07 | 1982-11-09 | Coulter Electronics, Inc. | Process for preparing whole blood reference controls having long term stability |
| US4338564A (en) | 1979-06-11 | 1982-07-06 | R & D Systems, Inc. | Hematology control composition and methods for its use |
| DE19634313A1 (de) * | 1996-08-24 | 1998-02-26 | Behringwerke Ag | Methode zur Stabilisierung von Plättchen |
| AU754936B2 (en) * | 1996-11-27 | 2002-11-28 | Aventis Pharmaceuticals Inc. | Pharmaceutical composition comprising a compound having anti-Xa activity and a platelet aggregation antagonist compound |
| US20070243632A1 (en) * | 2003-07-08 | 2007-10-18 | Coller Barry S | Methods for measuring platelet reactivity of patients that have received drug eluting stents |
| US7790362B2 (en) * | 2003-07-08 | 2010-09-07 | Accumetrics, Inc. | Controlled platelet activation to monitor therapy of ADP antagonists |
| DE10360628A1 (de) * | 2003-12-19 | 2005-07-21 | Dade Behring Marburg Gmbh | Kontrollplasma für Thrombinaktivitätstests |
| US7811558B2 (en) * | 2004-08-12 | 2010-10-12 | Cellphire, Inc. | Use of stabilized platelets as hemostatic agent |
| CN101072506B (zh) * | 2004-08-12 | 2010-05-12 | 塞尔菲乐有限公司 | 制备冻干血小板的方法、包括冻干血小板的组合物和使用方法 |
| JP5478884B2 (ja) * | 2005-09-26 | 2014-04-23 | ライフセル コーポレーション | 乾燥血小板組成物 |
| DE102006020385A1 (de) | 2006-04-28 | 2007-10-31 | Dade Behring Marburg Gmbh | Verfahren und Vorrichtung zur Bestimmung der Thrombozytenfunktion unter Flussbedingungen |
| DE102006020386A1 (de) * | 2006-04-28 | 2007-10-31 | Dade Behring Marburg Gmbh | Verfahren zur Bestimmung der Thrombozytenfunktion unter Flussbedingungen |
-
2011
- 2011-04-04 EP EP11160934A patent/EP2508892A1/de not_active Withdrawn
-
2012
- 2012-03-22 ES ES12160688.3T patent/ES2635196T3/es active Active
- 2012-03-22 EP EP12160688.3A patent/EP2508893B1/de active Active
- 2012-03-29 US US13/433,377 patent/US8741873B2/en active Active
- 2012-03-30 JP JP2012080672A patent/JP5947085B2/ja active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2012220493A5 (enExample) | ||
| Jin et al. | Endothelial activation and dysfunction in COVID-19: from basic mechanisms to potential therapeutic approaches | |
| Michels et al. | Imbalance of angiopoietin-1 and angiopoetin-2 in severe dengue and relationship with thrombocytopenia, endothelial activation, and vascular stability | |
| Palareti et al. | Activation of blood coagulation after abrupt or stepwise withdrawal of oral anticoagulants-a prospective study | |
| Fourrier | Severe sepsis, coagulation, and fibrinolysis: dead end or one way? | |
| Zhu et al. | IL-17 induces apoptosis of vascular endothelial cells—a potential mechanism for human acute coronary syndrome | |
| JP2015517305A5 (enExample) | ||
| Criado et al. | Lessons from dermatology about inflammatory responses in Covid‐19 | |
| Miyashita et al. | A three-phase approach for the early identification of acute lung injury induced by severe sepsis | |
| Augoustides | The inflammatory response to cardiac surgery with cardiopulmonary bypass: should steroid prophylaxis be routine? | |
| Moroi et al. | Akt and mitogen-activated protein kinase enhance C-type lectin-like receptor 2-mediated platelet activation by inhibition of glycogen synthase kinase 3α/β | |
| Ninivaggi et al. | Additive roles of platelets and fibrinogen in whole-blood fibrin clot formation upon dilution as assessed by thromboelastometry | |
| Balduini et al. | Constitutively released adenosine diphosphate regulates proplatelet formation by human megakaryocytes | |
| WO2012135671A3 (en) | Monoclonal antibodies against tissue factor pathway inhibitor (tfpi) | |
| Mohanty et al. | Anti-platelet agents in pediatric cardiac practice | |
| Mitchell et al. | Traumatic hemothorax blood contains elevated levels of microparticles that are prothrombotic but inhibit platelet aggregation | |
| Mann et al. | TACTIC: Trans‐Agency Consortium for Trauma‐Induced Coagulopathy | |
| Walsh et al. | Platelets protect cardiomyocytes from ischemic damage | |
| Fenger-Eriksen et al. | Fibrinogen concentrate and cryoprecipitate but not fresh frozen plasma correct low fibrinogen concentrations following in vitro haemodilution | |
| JP5947085B2 (ja) | 血小板活性試験のための対照及びキット | |
| Dionisio et al. | Redox Control in Platelet Activity and Therapy | |
| Davies et al. | The relationship between aortic aneurysm sac thrombus volume on coagulation, fibrinolysis and platelet activity | |
| Kau et al. | Activated protein C ameliorates Bacillus anthracis lethal toxin-induced lethal pathogenesis in rats | |
| Cubedo et al. | Erythrocyte-heme proteins and STEMI: implications in prognosis | |
| Secor et al. | Ascorbate inhibits platelet-endothelial adhesion in an in-vitro model of sepsis via reduced endothelial surface P-selectin expression |