Examples of using Globin in English and their translations into Vietnamese
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It's comprised of alpha globin and beta globin.
Beta thalassemia:when the body has an issue producing beta globin.
This condition occurs if all four alpha globin genes are missing or altered.
Alpha thalassemia:when the body has a problem producing alpha globin.
This condition develops when all four alpha globin genes are changed or missing.
People also translate
Beta thalassamia:It occurs when the body cannot produce beta globin.
Normally, the majority of adult hemoglobin(HbA) is composed of four protein chains,two α and two β globin chains arranged into a heterotetramer.
Four genes are needed to make enough alpha globin protein chains.
There are at least six genes that control globin synthesis in humans, resulting in the formation of six structurally different polypeptide chains that are designated α, β, γ, δ, ξ, and ς chains.
Individuals with this condition have one normal gene and one with a mutation,causing a mild decrease in beta globin production.
To blood: increases the number of white and red blood cell, hemoglobin, reticulocyte,blood platelet, globin, heightens PH reading, shortens blood forming time.
More in detail, Mediterranean anemia is due to the altered production of one ormore of the four protein chains(globins) that make up Hb.
The name hemoglobin is the concatenation of heme and globin, reflecting the fact that each subunit of hemoglobin is a globular protein with an embedded heme(or haem) group;
So, if one or both of the genes that tells chromosome 11 to produce beta globin is altered, less beta globin is made.
For example, the most common hemoglobin sequences in humans and chimpanzees are nearly identical,differing by only one amino acid in both the alpha and the beta globin protein chains.
There are two main types of thalassemia:Alpha thalassemia occurs when a gene or genes related to the alpha globin protein are missing or changed(mutated).
You must be sure to protect your stronghold from the attacking us Globins cursed with an archer and a number of soldiers have to defend your fortress, strategically added to[…].
In just a few seconds, his character rescues a girl standing next to him from a large brick falling in the first battle between Peter Parker(Tobey Maguire)and Green Globin(Willem Dafoe).
Beta thalassemia intermediamay likewise happen when both of the beta globin genes are altered, but the anomalies are less severe than those that normally cause beta thalassemia significant.
Cottonseed go through delinting, husking, low temperature softening, flaking, conditioning, leaching, degreasing, drying, toxic substance(gossypol) removal to produce cottonseed protein,which contains about 90 percent globin.
The severity of alpha and beta-thalassemia depends on how many of the four genes for alpha globin or two genes for beta-globin are missing.
In thalassemia, patients have defects in either the α or β globin chain, causing the production of abnormal red blood cells(In sickle-cell disease, the mutation is specific to β globin).
The severity of alpha and beta thalassemia relies upon on how among the four genes for alpha globin or two genes for beta globin are lacking.
Cottonseed go through delinting, husking, low temperature softening, flaking, conditioning, leaching, degreasing, drying, toxic substance(gossypol) removal to produce cottonseed protein,which contains about 90 percent globin.
The two conditions may overlap, however,since some conditions which cause abnormalities in globin proteins(hemoglobinopathy) also affect their production(thalassemia).
Hemoglobinopathies are simply structural abnormalities in the globin proteins themselves.[4] Thalassemias, in contrast, usually result in underproduction of normal globin proteins, often through mutations in regulatory genes.
These individuals have two abnormal genes that cause either a severe decrease orcomplete lack of beta globin production, preventing the production of significant amounts of normal hemoglobin(Hb A).
The one suffering from has two abnormal genes that lead to a severe decrease orcomplete absence of beta globin production, which prevent the creation of the required amounts of normal hemoglobin(Hb A).
The severity of the anemia caused by beta thalassemia depends on which mutations are present andwhether there is decreased beta globin production(called beta+ thalassemia) or if production is completely absent(called beta0 thalassemia).