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On the other hand, serous glands secrete lingual lipase whereas pancreatic juice is responsible for producing the pancreatic lipase.
Translocation - involves two…
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Download file to see previous pages des provides the template of a particular amino acid especially in reference to the subunit composed of a set of nucleobases of a DNA strand represented by A-adenine, C-cytosine, G-guanine, and T-thymine whose arrangement may be found variable while in covalent linkage along the phosphodiester nucleic acid backbone. About 90 distinct proteins serve as the minimum requirement for ‘translation’ to take place involving the coordinated action of mRNA, tRNA, soluble pools of amino acids, and ribosomes. Transcription is similarly affected by the nucleotide sequence through the nature of templated copying from nucleic acid to nucleic acid.
Sickle cell anemia refers to a genetically inherited disease that is characterized by abnormal, sickle-shaped red blood cells (erythrocytes), resulting from a point mutation in the hemoglobin gene. Basically, the condition is a recessive trait that requires two copies of the mutated allele to indicate symptoms which means that either both parents originally have sickle cell anemia or are carriers of the mutated allele from which a child may acquire the disease. This type of anemia poses a serious threat to health and general life of a person who may often encounter or become prone to breathlessness, jaundice, fatigue, paleness, susceptibility to infections, as well as pain in the back, leg and arm, and joints.
Individuals with sickle cell anemia possess a mutation in a gene on chromosome 11 that codes for the beta subunit of the hemoglobin protein. As a consequence, hemoglobin molecules do not undergo proper formation, causing the red blood cells to have rigid concave structure.
Two copies of mutated allele form the basis of obtaining the disease and these can only come from both parents who each must contribute a single copy so, with a father being a homozygous dominant (with normal hemoglobin) and a mother being heterozygous for the trait, the probability of acquiring the trait such that the offspring bears the disease or ...Download file to see next pagesRead More
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