Translation for 'sickle cell' from English to Russian

sickle cell

серповидная клетка {ж}биол.

---

sickle

серп {м}инстр.сель.

Advertisement

hammer and sickle

серп и молот {noun}пол.

cell

клетка {ж}биол.

cancerous cell

раковая клетка {ж}биол.мед.

cancer cell

раковая клетка {ж}биол.мед.

cell division

деление {с} клеткибиол.

stem cell

стволовая клетка {ж}биол.

cell biology

клеточная биология {ж}биол.наука

биология {ж} клеткибиол.наука

Wigner-Seitz cell

ячейка {ж} Вигнера-Зейтцаминерал.физ.хим.

red blood cell <RBC>

эритроцит {м}биол.мед.

• She conducted experiments on Mössbauer spectroscopy and its application in the study of sickle-cell anemia.
• Genetic tests are available for a number of genetic conditions, including but not limited to: Down syndrome, sickle cell disease, Tay–Sachs disease, muscular dystrophy.
• Amongst these include the discovery of kwashiorkor, the pioneer of treatments for pediatric sickle cell anemia and the invention of various spacecraft support systems.
• Diseases such as sickle cell disease that are caused by autosomal recessive disorders for which a person's normal phenotype or cell function may be restored in cells that have the disease by a normal copy of the gene that is mutated, may be a good candidate for gene therapy treatment.
• Some conditions such as sickle-cell disease and cystic fibrosis respectively confer immunity to malaria and resistance to cholera when a single copy of the recessive allele is contained within the genotype of the individual, so eliminating these genes is undesirable in places where such diseases are common.

• This mutation creates a "hydrophobic patch" on the protein surface that promotes intermolecular aggregation, the molecular event that gives rise to sickle-cell anemia.
• Routine vaccination against meningococcus is recommended by the Centers for Disease Control and Prevention for all 11- to 18-year-olds and people who have poor splenic function (who, for example, have had their spleen removed or who have sickle-cell disease which damages the spleen), or who have certain immune disorders, such as a complement deficiency.
• Causes of low-flow priapism include sickle cell anemia (most common in children), leukemia, and other blood dyscrasias such as thalassemia and multiple myeloma, and the use of various drugs, as well as cancers.
• Hemolytic crises are a major concern with sickle-cell disease and G6PD deficiency.
• His discovery of sickle cell anemia as a "molecular disease" opened the way toward examining genetically acquired mutations at a molecular level.

• Changes to viscosity has been shown to be linked with diseases like hyperviscosity, hypertension, sickle cell anemia, and diabetes.
• Mutations within a single gene have been identified as a cause of multiple diseases, including sickle cell disease, known as single gene disorders.
• It is also used to prevent bacterial endocarditis and as a pain-reliever in high-risk people having dental work done, to prevent "Streptococcus pneumoniae" and other encapsulated bacterial infections in those without spleens, such as people with sickle-cell disease, and for both the prevention and the treatment of anthrax.
• Several genetic factors provide some resistance to it including sickle cell trait, thalassaemia traits, glucose-6-phosphate dehydrogenase deficiency, and the absence of Duffy antigens on red blood cells.
• One-third of all indigenous inhabitants of Sub-Saharan Africa carry the allele, because, in areas where malaria is common, there is a survival value in carrying only a single sickle-cell allele (sickle cell trait).

• The alpha chain of hemoglobin contains 146 amino acid residues; substitution of the glutamate residue at position 6 with a valine residue changes the behavior of hemoglobin so much that it results in sickle-cell disease.