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Sentences for "chromosome "
The chromosome in question is the second-smallest of the 23 pairs in a human cell.
Or consider Robin Cook's thriller Chromosome 6 .
Today he is gene SLC6A4, whose specific Olympian dwelling place is chromosome 17q12.
This work is presumably as definitive as the LSD chromosome damage studies much published in Life magazine in 1967 and 1968.
Le Monde of Paris, which also reported the development on its front page, said the magazine Nature is due to publish the composition of Chromosome 22 this Thursday, marking the first time that the hugely complex chemical structure of a complete human chromosome has been revealed.
"The genetic code in the chromosome is thought to contain vital information on several hereditary conditions, including schizophrenia and deafness," the Sunday Telegraph of London said.
It added, "The 22 nd chromosome is also a key immune system regulator.
txt My Professor the Plagiarist The Human Decoder Ring Chromosome 22 has been almost completely decoded by an international team of scientists.
As reported in a recent issue of Nature , the very first sequenced chromosome may offer new insights into many human diseases, including schizophrenia.
) The researchers, who hail from Australia, Britain, Japan, New Zealand, Sweden, and the United States, discovered that Chromosome 22 contains 33.
In genetic recombination, the double chromosome complement sets, maternal and paternal homologues, pair up, break and recombine to yield oVspring chromosomes the left half of which derives from one parental chromosome, the right half of which derives from the other parental chromosome.
But, with mating and recombination, a rabbit with A on the left end of a maternal chromosome, and B on the right end of the homologous paternal chromosome might experience recombination.
One of them contains introns, exons and classic regulatory signals, while the remaining five are intronless genes [ 59 ] located on chromosome 2 [ 66 ] .
In addition, pop1 mutants display an increased rate of chromosome loss, a phenotype that is not easily explained by accumulation of Rum1p and Cdc18p [ 23 ] .
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