The answer to this question would be: vertebrae
In vertebrae fracture, traction is important to assure immobilization of the vertebrae. Movement can cause the fragment of bone in the fracture damaging the neural tissue in the vertebrae.
To ensure no movement in the neck, metal tongs can be put on the skull. The tongs will help fixate the skull with the shoulder.
Answer:
Decrease
Explanation:
If the foxes have nothing to eat, some will starve and die so the population will decrease.
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I believe the answer is Frictional Force
Neutrophils They kill and then digest the bacteria and the fungi. They are the most numerous type of the white blood cell and your first line of the defense when the infection strikes.
A high level of neutrophils in the blood is called neutrophilia. This is a sign that your body is infected. Neutrophilia can indicate many underlying conditions and factors, including: Infection, possibly bacteria. They capture and destroy invading microbes through phagocytosis and intracellular degradation, release of granules, and formation of neutrophil extracellular traps upon detection of pathogens. Neutrophils are also involved as inflammatory mediators. What is the most common cause of high neutrophils? infection. This is the most common cause of high neutrophil counts. Most bacterial infections cause elevated neutrophil counts, but not all. Viral infections generally do not cause neutrophilia, but it can occur early in the infection.
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Answer:
SNPs have shown that only 0.1 % of DNA sequences are different in the human genome between different individuals, thereby all the inherited phenotypic variation observed in our species is associated with only 0.1 % of differences at the genome level
Explanation:
Haplotypes are block-like sequences of DNA that are inherited together due to low recombination rates. Moreover, single-nucleotide polymorphism (SNP) mapping is a very useful methodology used to map the site of SNP mutations (i.e., SNP variants). In this regard, it has been observed that there are approximately 10 million common SNPs in the human genome. These SNPs contribute to the wide range of phenotypic variation observed in human populations for different traits (e.g., eye color, hair, weight, height, etc). Moreover, researchers have determined that SNPs can be clustered into haplotypes, thereby haplotypes can be accurately sampled by as few as approx. 300,000 selected SNPs, which are sufficient to represent all of the genetic variation across different human genomes.
