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Blood and Hemostasis

AB
ABOmost commonly used blood groups and typing
Albuminblood protein that maintains osmotic pressure
Anemiacondition with not enough RBCs and/or hemoglobin
Antibodiesproteins found in plasma that react with antigens; agglutinins
Anticoagulantsubstance that inhibits clotting
Antigensprotein markers found on RBCs; agglutinogens
Anucleateno nucleus
Bloodfluid connective tissue
Blood dopingdrugs or transfusions which enhance the number of RBCs
Chemotaxischemical attraction of WBCs to disease or injury site
Clottingcoagulation; process that produces clot; involves clotting factors
Cross matchmixing of donor and recipient blood to test compatibility
Embolusmoving clot
EmigrationWBCs leaving the blood stream
EosinophilWBC with red staining granules; can emigrate; becomes wandering macrophage
Erythrocytered blood cell
Erythropoiesisformation of red blood cells
Erythropoietinproduced by the kidney; increases the number of RBC precursors
Extrinsicclotting pathway that occurs rapidly; clotting factor leaks into blood from cells outside vessels
Fibrinogenblood protein for clotting
Fibrinolyticsystem that dissolves small
Globulinsblood proteins that are part of the immune system
Hematocritblood test giving RBCs as a percentage of cells found in whole blood
Hematologyscience that studies blood
Hematopoiesisprocess of blood formation
Hemoglobinred protein in RBC that carries oxygen
Hemorrhageloss of large amounts of blood from vessels
Hemostasisblood clotting process
Hypoxiabody cells not getting enough oxygen
Interstitialfluid which bathes tissues
intrinsicclotting pathway that is more complex and occurs more slowly; activators are in the blood
leukemiamalignant cancer of the blood and bone marrow
leukocytewhite blood cell
leukocytosishigh WBC count due to microbes
leucopenialow WBC count due to radiation
lymphoidstem cells that give rise to lymphocytes
MHCantigens on WBCs that are unique for each individual (initials)
myeloidstem cells that give rise to RBCs
Sickle celltype of anemia in which a single amino acid error in the hemoglobin molecule causes the RBC to sickle
Thalassemiainherited disorder that produces abnormal alph or beta hemoglobin chains
Thrombocyteplatelet
Thrombopoietinhormone produced by the liver; stimulates formation of platelets
Thrombosisclot formed in a an unbroken vessel
Transfusiontransfer of whole blood or blood components
Typingdetermination of a blood type
Vascular spasmsmooth muscle contraction in small blood vessels; reduces blood loss for up to several hours



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