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Mrac [35]
3 years ago
11

He creationist and evolutionist are in agreement on all of the following items except:

Biology
1 answer:
adoni [48]3 years ago
5 0
<span>the ability of matter to be self organizing</span>
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Can somebody please do the first one and could someone do it quickly and correctly thanks!
Rufina [12.5K]

Answer:all grow and develops

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3 years ago
Helppp helpppppp plz I need help on the blank onesss
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3. B. deforestation

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5 0
4 years ago
If a population of 1,000 individuals has 160 rr genotypes, assuming simple dominance by the A allele, what is the frequency of t
OverLord2011 [107]
<span>Here square frequency of recessive alleles r^2 = 160/1000 = 0.16
   
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8 0
4 years ago
Which phrase is not an example of intercellular communication?
-Dominant- [34]

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bacteria share information about nutrients

8 0
3 years ago
Which genetic disorder causes the body to produce unusually thick mucus in the lungs and intestines?
galina1969 [7]

Answer: Cystic Fibrosis

Explanation:

Cystic fibrosis (abbreviated CF) is an autosomal recessive genetic disease that mainly affects the lungs, and to a lesser extent the pancreas, liver and intestine, causing an abnormally thick, sticky mucus to build up in these areas. This mucus collects in the airways of the lungs and pancreas.  The main cause of morbidity and mortality is pulmonary involvement, which accounts for 95% of deaths, mainly due to repeated infections caused by bronchial obstruction due to the secretion of very thick mucus.

This build up of mucus causes life-threatening lung infections and serious digestive problems.  It is one of the most common types of chronic lung disease in children and young adults, and is a life-threatening disorder; patients often die from lung infections due to <em>Pseudomonas</em> or <em>Staphylococcus</em>.

<u>It is a hereditary disease produced by a mutation in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This protein is involved in the passage of chlorine ion through cell membranes and its deficiency alters the production of sweat, gastric juices and mucus. </u>The disease develops when neither allele is functional. Over 1500 mutations have been described for this disease, most of which are small deletions or point mutations; less than 1% are due to mutations in the promoter or chromosomal rearrangements. However, many people carry the CF gene, but do not have any symptoms. This is because a person with this disease must inherit 2 defective genes, 1 from each parent.

<u>There is no curative treatment, however there are treatments that allow the improvement of symptoms and extend life expectancy. In severe cases, the worsening of the disease may necessitate a lung transplant.</u>

3 0
3 years ago
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