Answer:
1. Endocrine disrupters
Explanation:
Endocrine disrupters are chemicals that alters or interrupts the normal functioning of the endocrine system that consists of several glands that produce hormones responsible for various functions such as metabolism, reproduction, growth, etc. When this interferes with the endocrine system, it can bring about many undesirable consequences, one of which is low testosterone levels as reported in the Alligators in Florida lake that is polluted by high levels of dioxins. These chemicals act as endocrine disrupters.
1. The action that would control bleeding through the use of pressure points is B. push the main artery against a bone.
2. A. Confusion is a sign of heatstroke.
<span>Lafora disease is the most severe teenage-onset progressive epilepsy, a unique form of glycogenosis with perikaryal accumulation of an abnormal form of glycogen, and a neurodegenerative disorder exhibiting an unusual generalized organellar disintegration. The disease is caused by mutations of the EPM2A gene, which encodes two isoforms of the laforin protein tyrosine phosphatase, having alternate carboxyl termini, one localized in the cytoplasm (endoplasmic reticulum) and the other in the nucleus. To date, all documented disease mutations, including the knockout mouse model deletion, have been in the segment of the protein common to both isoforms. It is therefore not known whether dysfunction of the cytoplasmic, nuclear, or both isoforms leads to the disease. In the present work, we identify six novel mutations, one of which, c.950insT (Q319fs), is the first mutation specific to the cytoplasmic laforin isoform, implicating this isoform in disease pathogenesis. To confirm this mutation's deleterious effect on laforin, we studied the resultant protein's subcellular localization and function and show a drastic reduction in its phosphatase activity, despite maintenance of its location at the endoplasmic reticulum.
I got my information from </span>https://www.ncbi.nlm.nih.gov/pubmed/14722920
The deeper down you get, the colder the water is
Answer: Four amino acids.
Explanation:
RNA (ribonucleic acid) and DNA (deoxyribonucleic acid) are polymers made up of long chains of nucleotides. Thus, a nucleotide is the basic building block of nucleic acids and consists of a sugar molecule (ribose in RNA or deoxyribose in DNA) linked to a phosphate group and a nitrogenous base. <u>The nitrogenous bases can be Adenine (A), Thymine (T), Cytosine (C), Guanine (G) or Uracil (U) replacing T in RNA</u>. DNA is the molecule that stores the genetic information to synthesize polypeptides or proteins (set of amino acids). When proteins need to be created, DNA is transcribed into RNA and this RNA is translated in ribosomes to create polypeptides.
Complementarity is the ability to combine with their complement. A and T (or U) are complementary, while C and G are complementary to each other. Complementarity is the principle of replication and transcription, because it is a propery of both DNA and RNA sequences. Their the nucleotide bases at each position of the sequences are complementary, allowing cells to copy information.
Nucleotides in RNA are grouped into codons, which consist of groups of 3 nucleotides where each codon codes for an amino acid. Therefore, <u>the sequence of bases in nucleic acids determines which protein will be synthesized</u>. Protein synthesis begins with a start codon (AUG, which codes for the amino acid methionine) and ends with a stop codon (UGA, UAG and UAA). So, if there are 15 nucleotides, there are 15 bases. Since they are grouped in groups of 3, we will have a polypeptide of 4 amino acids.
<u>3 nucleotides form a codon, so 12 nucleotides form 4 codons giving 4 amino acids. The last codon, is formed by the last 3 nucleotides and form the stop codon that stop protein synthesis</u>.