Answer:
At the beginning you start out with a lot of energy and stamina but as you progress, maybe five minutes in, you start to get out of breath. While breathing harder, you are trying to intake more oxygen and at the 10 minute mark you can feel your muscles burning a little bit and tire out more. At this point you are gasping for oxygen because your muscles are deprived of oxygen and you body makes lactic acids which you muscles can use instead of oxygen. By the end of it you are very tired.
Explanation:
Hope this helps! I am not sure how scientific of an explanation you wanted.
To help the nervous system and brain develop.
Answer:
Receiving sensory information and carrying commands to the muscles.
Explanation:
The spinal cord serves as the transmission conduit for the passage of action potential as sensory information through the sensory/afferent neurons to the dorsal roots of the spinal cord.The information synapse with the inter neurons,branching off to the brain and emerged as the response through the motor/efferent neurons to the effectors(muscles).
This pathways is called reflex arc. Thus most of the involuntary action of the body is conducted through the spinal cord
Euglena are a unicellular organism. They are classified into the Kingdom Protista. They are then further classified into the Phylum<span> Euglenophyta. All euglena can make their own food by photosynthesis.</span>
Answer:
One-half of the daughters of an affected man would have this condition.
Explanation:
Each daughter born to a woman that is positive for a dystrophin mutation on one of her two X chromosomes possess a 50 percent likelihood of possessing the mutation and also becoming a carrier. Carriers at times do not show the disease symptoms but may give birth to a child that has the mutation or the disease condition. DMD carriers do have a higher chance of cardiomyopathy.
A man with DMD cannot transfer the affected gene to his sons since he passes to his son a Y chromosome, not the X chromosome. But he will definately transfer it to his daughters, since each daughter possess her father’s only X chromosome resulting in the daughters being carriers.
Hence, One-half of the daughters of an affected father and a carrier mother could have this condition.
