Embryology provides evidence for evolution because during their development, many organisms look similar, suggesting that very different organisms may have a common ancestor.
Answer:
erosion and a, weatheri g and b
The correct answer is the "superior temporal sulcus".
Superior Temporal Sulcus is described as the sulcus isolating the advanced temporal gyrus from the middle temporal gyrus in the temporal lobe of the brain. The advanced temporal sulcus is the primary sulcus not so good as the lateral fissure. latest research monitor multisensory processing talents. Studies has shown the recorded activation in the STS because of 5 precise social inputs, and therefore the STS is believed to be implicated in social perception.
Answer:
I am writing this in response to a letter regarding evolution. Evolution is increasingly solid, not shaky. Darwin’s “theory” or explanation was a way of understanding what he had discovered (which did not include genes, chromosomes, DNA or nucleotide bases). Our explanations now include genetics and the commonality of mutation.
Proofs are solid, not in question by serious scientists. Direct observation is one, which we see in the fact that this year’s flu evolved a little too far from last year’s, so flu shots are less effective this year than we would like them to be.
Fossils tell the story well: whales with legs, dinosaurs with feathers and Tiktaalik. The latter was found in the Canadian north and is part fish, part amphibian, before there were ever any amphibians. Imperfection is a good proof: think of your useless appendix, the very bad design of your ankles, knees, and back (talk to a chiropractor about that). You have big toes because they used to be useful thumbs for your grasping feet.
Many other animals and even plants similarly have flaws that show their evolutionary past. Two large human chromosomes reflect the coming together of two chimpanzee chromosomes each.
Hope it helps,
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Thank you
Answer:
I think the question is "How might an RNA-based genome results display an increased in infection rate?" because current statement doesn't convey a message clearly.
Explanation:
To answer this question, we need to understand first that what is gene expression. Gene expression is a process in which genetic information is transcribed first to RNA and then into proteins. During transcription stage, only active genes would be transcribed to RNA and all other DNA material don't transcribe at all. Now, if there is an infection, host cell would express only those genes which would actively take part in the defense mechanism, e.g. R-genes, genes involved in production of reactive oxygen species, etc. Hence, to monitor the infection rate, we will look at the RNA-based genome. To do this, we will extract the total RNA and then would sequence it. Then we will annotate the genes and check the relative abundance (differential expression). Finally, we would have a clear that these genes were active against the infection. By doing temporal sampling and sequencing, we would be able to measure the rate as well.
For the second part, potential complications that could arise in doing analysis is the lower amount of RNA, or rapid degradation of RNA in case of presence of RNAses. RNA can be degraded easily at room temperature.
