Pragma <span>is not one of rusbult and colleagues' (1986, 1987, 1998) three ways of coping with a failing relationship.
</span>Pragma<span> is a pragmatic, practical, mutually beneficial relationship. The EVLN framework was developed by rustbult and her colleagues for personal love and marriage relationships.</span>
Answer:
Oxidation of NADH by electron transport chain ensures a continuous supply of NAD+ for glycolysis.
Explanation:
To continue the process of glycolysis, cells must have a continuous supply of NAD+ which is required during one of the reactions of the payoff phase of glycolysis. Two molecules of NADH are formed per glucose molecule during glycolysis. The NADH gives its electrons to the terminal electron acceptors (O2) via electron transport chain. This ensures that the process of glycolysis is continued in cells to breakdown the glucose into pyruvate.
Answer:
on the outer surface of the red blood cell membrane
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.
Well, basically we can say that <span>Best Disease expresses itself more through the generations. The reason for that is because it is dominant. While we may say that the allele of the sickle cell anemia its indeed a recessive trait with 0% of chances, Best desease is a dominant trait with 50% of chances.</span>
