erythropoietic sentence in Hindi
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- Erythropoietic porphyria is a genetic disease resulting in the deposition of porphyrins throughout the body.
- Defects in ferrochelatase create a buildup of protoporphyrin IX, causing erythropoietic protoporphyria ( EPP ).
- A deficiency is associated with Gunther's disease, also known as congenital erythropoietic porphyria ( CEP ).
- The pain, burning, swelling, and itching that occur in erythropoietic porphyrias generally require avoidance of bright sunlight.
- The rarest is congenital erythropoietic porphyria ( C . E . P ), otherwise known as Gunther's disease.
- Erythropoietin is the primary erythropoietic factor that cooperates with various other growth factors ( e . g ., multipotent progenitors.
- It should also be noted that quite a bit of research emphesis is on non erythropoietic but, neuroprotective Peptides of Erythropoietin.
- This suggests a possible extra-ribosomal function for this gene in erythropoietic differentiation and proliferation, in addition to its ribosomal function.
- Peptide of Epo with amino acids 92-111 is neuroprotective while its erythropoietic potency is 10 fold less than the wild type.
- The U . S . Food and Drug Administration have recognized afamelanotide as an orphan drug for the treatment of EPP and congenital erythropoietic porphyria.
- Congenital erythropoietic porphyria ( Gunther disease ) is a rare congenital form of porphyria, and may be associated with red or brown discolored teeth.
- X-linked sideroblastic anemia or " X-linked dominant erythropoietic protoporphyria ", associated with ALAS2 ( aminolevulinic acid synthase ), has also been described.
- In the 9th episode of season 3 of " Finding Judas ", the primary patient is a young girl who is ultimately diagnosed with erythropoietic protoporphyria.
- Protoporphyrin IX as a direct precursor of heme is accumulated by patients of erythropoietic protoporphyria, which is one of the genetic disorders of the biosynthesis of the heme-pathway.
- Physiologically, porphyrias are classified as liver or erythropoietic based on the sites of accumulation of heme precursors, either in the liver or in the bone marrow and red blood cells.
- Carotenoderma is deliberately caused by beta-carotenoid treatment of certain photo-sensitive dermatitis diseases such as erythropoietic protoporphyria, where beta carotene is prescribed in quantities which discolor the skin.
- Winchester RJ, Meyers PA, Broxmeyer HE, Wang, CY, Moore MAS and Kunkel HG . Inhibition of human erythropoietic colony formation in culture by treatment with 1a antisera.
- With the exception of mammals, all vertebrate organisms have hemoglobin-containing cells in their blood and all of these red blood cells contain a erythropoietic lineage and in pathological states.
- A short peptide sequence from the erythropoietin molecule called JM4, has been found to be non-erythropoietic yet theoretically neuroprotective and is being readied for Stage 1 and 2 clinical studies.
- This variant of haploinsufficiency is only seen in two other human diseases : Erythropoietic protoporphyria, caused by mutations in the FECH gene; and hereditary elliptocytosis, caused by mutations in the spectrin gene.
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