Answer:
There is no cure for cystic fibrosis, but treatment can ease symptoms and reduce complications.
Explanation:
1). For those with cystic fibrosis who have certain gene mutations, doctors may recommend a newer medication called ivacaftor. This medication may improve lung function and weight, increases the activity of Cystic fibrosis transmembrane conductance regulator (CFTR)protein and reduce the amount of salt in sweat. It has been approved by the Food and Drug Administration for people with cystic fibrosis who are age 6 and older. The dose depends on your weight and age.
2). For people with a certain gene mutation who are age 12 and older, another drug is available that combines ivacaftor with a medication called lumacaftor. This drug is called orkambi.
The use of Orkambi may improve lung function and reduce the risk of exacerbations.
I hope you're clear on this Daxxy
Answer:
DNA sequences similarity among various organisms may be used to establish evolutionary relationship among living organisms. ... Organisms or animals whose DNA sequences are similar share common evolutionary origin.
Explanation:
Where’s the article?
I can’t tell what it’s about from the answers
Dendrites is 1
Soma is 2
Nylon sheeth is 3
Node of Ranvier is 4
Synapse is 5
Answer:
50%
Explanation:
Let's assume that the allele "T" gives the normal phenotype while the recessive allele "t" imparts the disease and is lethal in homozygous condition. The genotype of each of the two carrier parents would be "Tt". A cross between Tt and Tt would give the progeny in the following genotype ratio=
Tt x Tt= 1/4 TT: 1/2 Tt: 1/4 tt
Therefore, 1/2 or 50% progeny would be the carrier for the Tay-Sachs disease.
