haptoglobin वाक्य
उदाहरण वाक्य
मोबाइल
- Since the reticuloendothelial system will remove the haptoglobin-hemoglobin complex from the body, haptoglobin levels will be decreased in hemolytic anemias.
- Since the reticuloendothelial system will remove the haptoglobin-hemoglobin complex from the body, haptoglobin levels will be decreased in hemolytic anemias.
- In the process of binding hemoglobin, haptoglobin sequesters the iron within hemoglobin, preventing iron-utilizing bacteria from benefiting from hemolysis.
- This gene encodes a preproprotein that is processed to yield both alpha and beta chains, which subsequently combines as a tetramer to produce haptoglobin.
- The protein, called haptoglobin, could be used in future tests to detect this malignancy, which is usually far advanced by the time it is discovered.
- Hpr is 91 % identical to haptoglobin ( Hp ), an abundant acute phase serum protein, which possesses a high affinity for haemoglobin ( Hb ).
- The typical tests used for this are a CBC with peripheral smear, bilirubin, LDH ( in particular with isoenzyme 1 ), haptoglobin and urine hemoglobin.
- A positive test result occurs when the haptoglobin binding capacity of the blood is saturated, leading to heme released from cell free hemoglobin to bind to albumin.
- Free hemoglobin can bind to haptoglobin, and the complex is cleared from the circulation; thus, a decrease in haptoglobin can support a diagnosis of hemolytic anemia.
- Free hemoglobin can bind to haptoglobin, and the complex is cleared from the circulation; thus, a decrease in haptoglobin can support a diagnosis of hemolytic anemia.
- In blood plasma, haptoglobin binds free hemoglobin ( Hb ) released from erythrocytes with high complex will then be removed by the reticuloendothelial system ( mostly the spleen ).
- She traced this 16q fragile site through a multigenerational family and, together with Hecht and Everett Lovrien, she linked the 16q fragile site to the gene for haptoglobin.
- In severe extra-vascular hemolysis, haptoglobin levels can also be low, when large amount of hemoglobin in the reticuloendothelial system leads to transfer of free hemoglobin into plasma.
- The first step in the killing mechanism is the binding of TLF to high affinity receptors the haptoglobin-hemoglobin receptors that are located in the flagellar pocket of the parasite.
- The second research focus was on gene product analysis, where he used starch gel electrophoresis to explore the genetic diversity of plasma proteins ( such as haptoglobins and transferrins ).
- Under normal conditions the formation of haptoglobin-hemoglobin complexes prevents glomerular filtration, but if the hemolysis is extensive haptoglobin s uptake capacity is exceeded and hemoglobin can appear in urine.
- However, if you have the misfortune to possess the genotype haptoglobin 2-1, the study shows that this same treatment can drastically decrease your HDL function and cause cardiovascular disease.
- The mapping of haptoglobin to 16q was the second instance in which a human gene was mapped to a specific autosome ( non-sex chromosome ), presaging the Human Genome Project.
- A decrease in haptoglobin can support a diagnosis of hemolytic anemia, especially when correlated with a decreased red blood cell count, hemoglobin, and hematocrit, and also an increased reticulocyte count.
- The protein components of TLF-1 are haptoglobin related protein ( HPR ), apolipoprotein L-1 ( apoL-1 ) and apolipoprotein A-1 ( apoA-1 ).
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