acrocentric chromosome oor Spaans
acrocentric chromosome
en
a chromosome with the centromere near one end so that one chromosomal arm is short and one is long
Vertalings in die woordeboek Engels - Spaans
cromosoma acrocéntrico
Geskatte vertalings
Vertoon algoritmies gegenereerde vertalings
voorbeelde
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The NOR staining pattern of acrocentric chromosomes is consistent within an individual and is heritable.
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Centric fusion of the long arms of the two acrocentric chromosomes creates the unique chromosome.
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On the right is a chromosome 13 pair that is an example of an acrocentric chromosome.
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Robertsonian: A special type of translocation that involves two acrocentric chromosomes.
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E, Robertsonian translocation between two acrocentric chromosomes.
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Acrocentric chromosomes contain a very small short arm, stalks, and satellite DNA.
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C-banding stains the constitutive heterochromatin, which usually lies near the centromere, and NOR staining highlights the satellites and stalks of acrocentric chromosomes.
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Karyotypes of Mugil liza and M. curema from Venezuela were studied. M. liza karyotype is 2n=48 acrocentric chromosomes, but M. curema is 2n=24, containing one submetacentric and 11 metacentric pairs.
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We report 4 sires belonging to the Romosinuano breed (40%) and 10 bulls of the Casanareño breed (100%) with acrocentric Y chromosome which is characteristic of Bos taurus. This finding indicates a high degree of genetic introgression in these two breeds probably caused by the continuous input of zebu stallions in the Colombian Creole breeds.
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The X chromosome is subtelocentric (with one pair of long arms and one pair of short arms) and the Y chromosome is acrocentric (with only one pair of arms, or with a minute second pair).
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In the human, the short arms of the acrocentric chromosomes, which are mainly formed from heterochromatin, carry the nucleolar organiser regions.
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The X chromosome was found to be a medium-sized submetacentric chromosome, whereas the Y was a small acrocentric chromosome (Figure 2A).
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The ordering of the homologue chromosomes allowed the classification according to the international nomenclature as follows: 1 acrocentric pair, 3 submetacentric pairs, 1 metacentric pair and 19 subtelocentric pairs including sexual chromosomes X and Y.
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A Robertsonian translocation results when the long arms of two acrocentric chromosomes fuse at the centromere and the two short arms are lost.
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I first aim at showing the role of some so-called non homologous or homologous Robertsonian translocations or centric fusions of acrocentric chromosomes.
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Karyotipe formula is made up with 5 metacentric, 10 submetacentric and 10 subtelo-acrocentric chromosomes pairs, with a fundamental number of 80 in both sexes.
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If on the contrary the Robertsonian translocation is between chromosome 21 and any of the acrocentric chromosomes 13, 14, 15, 21 or 22, two situations can arise:
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Robertsonian translocations involve the long arm of acrocentric chromosomes with chromosomes13q;4q being predominantly involved. This defect can be transmitted along several generations, giving rise to chromosomally abnormal products with complete aneuploidy.
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In humans, the short arms of the acrocentric chromosomes, mainly formed from heterochromatin, are frequently associated in the interphase nucleus with other chromosomes having a large HC block (1, 9 and 16).
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In humans, the short arms of the acrocentric chromosomes, mainly formed from heterochromatin, are frequently associated in the interphase nucleus with other chromosomes having a large HC block (1, 9 and 16).
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The chromosomes were classified into three groups according to size and morphology: A metacentric, B submetacentric, and C acrocentric.
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Background. Robertsonian translocations involve the long arm of acrocentric chromosomes with chromosomes13q;4q being predominantly involved. This defect can be transmitted along several generations, giving rise to chromosomally abnormal products with complete aneuploidy.
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This synthesis is carried out starting from repeated genes, few hundred of times, in the genome and all are located at the short arms of acrocentric chromosomes (chromosomes 13, 14, 15, 21 and 22).
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Their children, however, may either be normal and carry the fusion chromosome (depending which chromosome is represented in the gamete), or they may inherit a missing or extra long arm of an acrocentric chromosome.
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The short, acrocentric human chromosomes, called group G in the human chromosome classification.
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