1answer.
Ask question
Login Signup
Ask question
All categories
  • English
  • Mathematics
  • Social Studies
  • Business
  • History
  • Health
  • Geography
  • Biology
  • Physics
  • Chemistry
  • Computers and Technology
  • Arts
  • World Languages
  • Spanish
  • French
  • German
  • Advanced Placement (AP)
  • SAT
  • Medicine
  • Law
  • Engineering
levacccp [35]
3 years ago
10

While human cells have a number of mechanisms to repair damaged DNA, these mechanisms are not perfect. Describe two conditions o

r diseases related to faulty or absent DNA repair.
Biology
1 answer:
amm18123 years ago
7 0

Answer:

1). Xeroderma pigmentation.

2). Ataxia-telangiectasia.

Explanation:

DNA repair processes include all the processes, which help in identification and correction of errors or damages in DNA. Defects in DNA repair mechanisms that increase risks for developing cancers and various other disorders. Two conditions related to faulty DNA repair are:

1). Xeroderma pigmentation (XP): XP can be defined as a genetic disorder, due to mutations in genes involved in repair processes. It leads to severe sunburn and freckling due to sun exposure, dry skin and skin pigmentation. People having xeroderma pigmentation are prone for skin cancer.

2). Ataxia-telangiectasia (AT): AT is caused bu mutation in ATM gene (ataxia-telangiectasia mutated) gene, which in involved in nucleotide-excision repair pathway. It leads to severe disability in children and increases risk for developing lymphomas and leukemia.

 

 

You might be interested in
pick at minimum 5 of your favorite foods from listed restaurants and list the food and calorie intake. Write a paragraph summari
Zepler [3.9K]

Answer:

-Pizza

-Lasagna

-Steak

-Salad

-Tomato Soup

It surprised me that there are 687 types of pizza in the world. There are so many types, and I have only tried about 15! It is crazy!

Explanation:

My mind!

5 0
3 years ago
Achondroplasia is a form of dwarfism in humans. It is caused by a mutant allele of the fibroblast growth factor receptor gene (F
ozzi
<h2>The correct answer is explained below:</h2>

Explanation:

  • According to the question, achondroplasia, a form of dwarfism, is caused by a mutant allele of the fibroblast growth factor receptor (FGFR) encoding gene.
  • This achondroplasia trait is dominant in nature. This is because presence of a single copy of the mutant allele results in the development of a dwarf phenotype.
  • Let the dominant mutant allele for the trait be represented by: A.
  • Let the recessive normal allele for the trait be represented by: a.
  • The individual with aa genotype is normal.
  • The individual with Aa genotype shows dwarfism.
  • The individual with AA genotype dies before birth.
  • As per the question, two people having achondroplasia have the genotype Aa.
  • Gametes produced by each of the individuals are, A and a.
  • Mating these individuals, we get the following possible offspring,

                                                      A                          a

                                        A         AA                         Aa

                         Phenotype       Dies                     Dwarf

                                        a         Aa                          aa

                         Phenotype       Dwarf                   Normal

  • The genotypes and the phenotypes of the possible offspring are represent in the Punnett square above.
  • The probability of the child to have achondroplasia is: = \frac{2}{3}.
  • Since the child with AA genotype dies before birth so three (genotypes Aa and aa) out of four possible children survives.

8 0
3 years ago
Drag each label to the correct category.
Nikitich [7]

Answer:

Weight: newtons, kilograms and changes when gravity changes

Mass: does not change when gravity changes, the amount of matter in something, and a gravitational force

Hope I get this right :)

3 0
3 years ago
Smooth muscle cells lack which protein(s)?
LuckyWell [14K]

The correct answer is C. troponin only.

The smooth muscle cells contain similar elements like the cardiac and skeletal muscle cells including actin, myosin and tropomyosin but they contain troponin.

Smooth muscle tissues are non striated and produce their own connective tissue called endomysium. Smooth muscle cells also lack sarcomeres but have other thin and thick filaments along with actin and myosin contractile proteins.

Due to lack of troponin the cross bridge formation is regulated by the regulatory protein calmodulin instead of the troponin- tropomyosin complex.


3 0
4 years ago
Diagram shows the transport of respiratory gases in the human body.
miss Akunina [59]

Answer:

ai) P= Red blood cell   Q= Alveoli

ii)1. It gives the lungs a large surface area to volume ratio.

2. It is moist and thin.

b) P has a disc or biconcave shape which allows the O2 to bind to it with the help of a protein called haemoglobin for it to be transferred to various parts of the body.

c) Carbon monoxide will bind to the haemoglobin to form carboxyhaemoglobin causing oxygen disruption

3 0
3 years ago
Other questions:
  • Hydrocarbons are which type of macromolecule and what elements make them up?
    7·1 answer
  • Why can't you prescribe antibiotics to treat a viral infection?
    14·1 answer
  • What is the function of the;
    12·1 answer
  • A change in a sequence of DNA bases in a bacterial cell has resulted in a mutation. This mutation has increased the ability of t
    13·1 answer
  • Which of the following genotypes is homozygous dominant?
    7·1 answer
  • HELP ASSAP PLEASE
    9·2 answers
  • Please help the test is due in 20 mins
    5·2 answers
  • Larger lions have 15,000 kcal on average to expend per day and need to gain more than that to survive. If lions can only hunt le
    5·1 answer
  • If an organism is 2n=54, how many chromosomes will be in each if it's gametes?
    5·1 answer
  • True or False? Don’t understand.
    5·2 answers
Add answer
Login
Not registered? Fast signup
Signup
Login Signup
Ask question!