Answer:
The right side of the body
Explanation:
Skin-fold assessment are generally taken on the right side of the body
Answer:
The different skeletal muscle fiber types vary in the speed and duration of their twitches due to -
b) They vary in the rate of hydrolysis of ATP
c) They vary in the removal of Ca+ from the cytosol
Explanation:
There are mainly two types of muscle fibers , i.e.
a) slow twitching, long contraction duration( type I fibers)
b) First twitching but short duration of contraction. ( type II fibers).
Now think of the physiology of muscle. Two components are important, cytosolic Ca++ concentration and Availability of ATP. K+ is related to the action potential ( none or all law, there is no relation to the duration with respect to the potassium). For long contraction muscle fibers need a more steady supply of ATP, and also consistent high concentration of cytosolic Ca++ for muscle contraction to happen. So, these two factor is important for the duration of twitching. So the answer is option f .
Answer: Mutations in the GALT, GALK1, and GALE genes cause galactosemia.
Explanation: Galactosemia is a disorder that affects how the body processes a simple sugar called galactose. A small amount of galactose is present in many foods. It is primarily part of a larger sugar called lactose, which is found in all dairy products and many baby formulas. The signs and symptoms of galactosemia result from an inability to use galactose to produce energy.Classic galactosemia, also known as type I, is the most common and most severe form of the condition. If infants with classic galactosemia are not treated promptly with a low-galactose diet, life-threatening complications appear within a few days after birth. Affected infants typically develop feeding difficulties, a lack of energy (lethargy), a failure to gain weight and grow as expected (failure to thrive), yellowing of the skin and whites of the eyes (jaundice), liver damage, and abnormal bleeding. Other serious complications of this condition can include overwhelming bacterial infections (sepsis) and shock. Affected children are also at increased risk of delayed development, clouding of the lens of the eye (cataract), speech difficulties, and intellectual disability. Females with classic galactosemia may develop reproductive problems caused by an early loss of function of the ovaries (premature ovarian insufficiency). Galactosemia type II (also called galactokinase deficiency) and type III (also called galactose epimerase deficiency) cause different patterns of signs and symptoms. Galactosemia type II causes fewer medical problems than the classic type. Affected infants develop cataracts but otherwise experience few long-term complications. The signs and symptoms of galactosemia type III vary from mild to severe and can include cataracts, delayed growth and development, intellectual disability, liver disease, and kidney problems.
Emission
I hope this helped:))
Answer:pounds (lbs)
Explanation:
Lbs is the is measurement for weight
