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  2. Hemolysin - Wikipedia

    en.wikipedia.org/wiki/Hemolysin

    Hemolysins or haemolysins are lipids and proteins that cause lysis of red blood cells by disrupting the cell membrane.Although the lytic activity of some microbe-derived hemolysins on red blood cells may be of great importance for nutrient acquisition, many hemolysins produced by pathogens do not cause significant destruction of red blood cells during infection.

  3. Hemolytic anemia - Wikipedia

    en.wikipedia.org/wiki/Hemolytic_anemia

    Laboratory studies commonly used to investigate hemolytic anemia include blood tests for breakdown products of red blood cells, bilirubin and lactate dehydrogenase, a test for the free hemoglobin binding protein haptoglobin, and the direct Coombs test (also called direct antiglobulin test or DAT) to evaluate complement factors and/or antibodies ...

  4. Red blood cell - Wikipedia

    en.wikipedia.org/wiki/Red_blood_cell

    Red blood cells (RBCs), referred to as erythrocytes (from Ancient Greek erythros 'red' and kytos 'hollow vessel', with -cyte translated as 'cell' in modern usage) in academia and medical publishing, also known as red cells, [1] erythroid cells, and rarely haematids, are the most common type of blood cell and the vertebrate's principal means of delivering oxygen (O 2) to the body tissues—via ...

  5. Hemolysis - Wikipedia

    en.wikipedia.org/wiki/Hemolysis

    A red blood cell in a hypotonic solution, causing water to move into the cell A red blood cell in a hypertonic solution, causing water to move out of the cell. Hemolysis or haemolysis (/ h iː ˈ m ɒ l ɪ s ɪ s /), [1] also known by several other names, is the rupturing of red blood cells (erythrocytes) and the release of their contents into surrounding fluid (e.g. blood plasma).

  6. Anemia - Wikipedia

    en.wikipedia.org/wiki/Anemia

    Hereditary spherocytosis [35] is a hereditary defect that results in defects in the RBC cell membrane, causing the erythrocytes to be sequestered and destroyed by the spleen. Hereditary elliptocytosis [35] is another defect in membrane skeleton proteins. Abetalipoproteinemia, [35] causing defects in membrane lipids; Enzyme deficiencies

  7. Kell antigen system - Wikipedia

    en.wikipedia.org/wiki/Kell_antigen_system

    The encoded protein contains sequence and structural similarity to members of the neprilysin (M13) family of zinc endopeptidases. [6] There are several alleles of the gene which creates Kell protein. Two such alleles, K 1 (Kell) and K 2 (Cellano), are the most common. The kell protein is tightly bound to a second protein, XK, by a disulfide bond.

  8. Erythropoiesis - Wikipedia

    en.wikipedia.org/wiki/Erythropoiesis

    A feedback loop involving erythropoietin helps regulate the process of erythropoiesis so that, in non-disease states, the production of red blood cells is equal to the destruction of red blood cells and the red blood cell number is sufficient to sustain adequate tissue oxygen levels but not so high as to cause sludging, thrombosis, or stroke ...

  9. Cytochrome b5 reductase - Wikipedia

    en.wikipedia.org/wiki/Cytochrome_b5_reductase

    On erythrocytes, red blood cells, the c5br enzyme is responsible for the recycling and conversion of methemoglobin to hemoglobin. [6] Methemoglobin is an oxidized form of hemoglobin attached to a ferric-state iron (Fe3+), which can therefore not carry and deliver oxygen to tissues. [ 15 ]

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