NEET
Zoology

Gene Therapy

Low Priority
Consistency: 25%
Weightage: 5 / 20 Yrs

High-Yield Trend

1
2022
1
2021
1
2018
1
2016
1
2009

Questions
5 MCQs

01
PYQ 2009
easy
zoology ID: neet-200

The genetic defect-Adenosine Deaminase (ADA) deficiency may be cured permanently by:

1. periodic infusion of genetically engineered lymphocytes having functional ADA cDNA
2. administering adenosine deaminase activators
3. introducing bone marrow cells producing ADA into cells at early embryonic stages
4. invitro cell culture therapy
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02
PYQ 2016
easy
zoology ID: neet-201

Which kind of therapy was given in 1990 to a four-year-old girl with Adenosine Deaminase (ADA) deficiency?

1. Gene therapy

2. Chemotherapy

3. Immunotherapy

4. Radiation therapy

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03
PYQ 2018
easy
zoology ID: neet-201
Which of the following is commonly used as a vector for introducing a DNA fragment in human Lymphocytes?
1. Retrovirus
2. Ti plasmid
3. \lambda phage
4. pBR 322
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04
PYQ 2021
easy
zoology ID: neet-202

When gene targeting involving gene amplification is attempted in an individual's tissue to treat disease, it is known as:

1. Molecular diagnosis 2. Safety testing
3. Biopiracy 4. Gene therapy
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05
PYQ 2022
easy
zoology ID: neet-202
In gene therapy of Adenosine Deaminase (ADA) deficiency, the patient requires periodic infusion of genetically engineered lymphocytes because:
1. Genetically engineered lymphocytes are not immortal cells.
2. Retroviral vector is introduced into these lymphocytes.
3. Gene isolated from marrow cells producing ADA is introduced into cells at embryonic stages
4. Lymphocytes from patient's blood are grown in culture, outside the body.
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