There are 306 bones in the human body. babies start out with 300 bones, when they grow up these bones grow together to make one large bone. by the time your an adult you'll have exactly 206 bones. half of these bones can be found in your hands and feet!
All of the following contributes to turbulent blood flow except third and fourth heart sounds.
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Explanation:</u></h3>
The blood flow in human body is always described to be laminar. Some conditions cause the high flow when there is an ascending aorta. This causes the laminar flow of blood into turbulent. When this occurs the flow of the blood will not be smooth and linear.
When the kinetic energy in the fluid flow increases the turbulent flow of blood occurs. Both the magnitude and the direction of the flow changes in this type of blood flow. These are caused by the irregularities in the vessel walls, flow rates to ne higher and opening of the valves of the heart.
Answer:
b. a semi-permeable double layer of phospholipids that have hydrophilic heads and hydrophobic tails
Explanation:
B is correct as the cell membrane is selectively semi-permeable. It is selectively semi-permeable because this quality allows it to control what can and can't enter the cell, and how it does so.
The cell membrane also has a phospholipid bi-layer comprised of a double layer of phospholipids which have hydrophilic head and hydrophobic tails. This is because the heads are made of phosphate and are polar and are therefore attracted to water (hydrophilic), while the tails are made of lipids (i.e. fats, oils) which do not mix with water and are therefore hydrophobic.
The properties of each phospholipid is also why they form the double layer structure, the hydrophilic heads naturally face outwards into the water and protect the hydrophobic tails on the inside.
Hope this helped!
Wrinkled seeds because every single trait is recessive
Answer: DF508 mutation. A Genetic, Hereditary, Autosomal and Recessive Mutation.
Explanation:
Cystic fibrosis (CF) is a recessive autosomal lethal disease, it is most common on Caucasoid populations. Its diagnosis is suggested by the clinical features of chronic obstructive pulmonary disease, persistent pulmonary colonization (particularly with mucoid Pseudomonas strains), meconium ileus, pancreatic insufficiency with or familiarity history of the disease. The FC gene is large, with about 250 Kb of genomic DNA, 27 exons representing about 5% of genomic DNA; encodes a 6.5 kb transcribed mRNA. This mRNA is transcribed into a protein of 1480 amino acid called CFTR (Regulator Transmembrane Conductance Cystic Fibrosis). When a three-base pair deletion, adenosine-thymine-thymine (ATT) identified in the CFTR gene, exon 10, it results in the loss of a single amino acid phenylalanine at position 508 of the protein. This mutation is called DF508; “D” stands for deletion and “F” for phenylalanine amino acid.
