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#Question id: 7176


The metamorphic changes of frog development are brought about by following events.

(A) the secretion of the hormone thyroxine (T4) into the blood by the thyroid gland

(B) the degradation of T3 in the target tissues

(C) the conversion of (T4) into the more active hormone, triiodothyronine (T3) by the target tissues

Which of the following series is correct?

#Unit 5. Developmental Biology
  1. AàBàC
  2. BàAàC
  3. AàCàB
  4. CàAàB
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TLS Online TPP Program

#Question id: 17269

#Unit 8. Inheritance Biology

In humans, albinism (unpigmented skin, hair, and eyes) is due to an enzymatic deficiency, and it is an autosomal recessive trait. Suppose that in a small country of one million people (“Generation 1”), there are 500 aa albinos and 9000 Aa heterozygous carriers. In the next generation of 1 million individuals (Generation 2), what are the expected numbers of aa albinos and Aa carriers? (Assume random mating and all other HardyWeinberg conditions.)

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#Question id: 17807

#Unit 8. Inheritance Biology

In humans, albinism (unpigmented skin, hair, and eyes) is due to an enzymatic deficiency, and it is an autosomal recessive trait. Suppose that in a small country of one million people (“Generation 1”), there are 500 aa albinos and 9000 Aa heterozygous carriers. What is the probability that a child will be albino if: Both parents are non-albino members of Generation 2?

TLS Online TPP Program

#Question id: 17808

#Unit 8. Inheritance Biology

In humans, albinism (unpigmented skin, hair, and eyes) is due to an enzymatic deficiency, and it is an autosomal recessive trait. Suppose that in a small country of one million people (“Generation 1”), there are 500 aa albinos and 9000 Aa heterozygous carriers. What is the probability that a child will be albino if: One parent is a non-albino member of Generation 2, and the other parent is a non-albino member of Generation 1.

TLS Online TPP Program

#Question id: 17809

#Unit 8. Inheritance Biology

In humans, albinism (unpigmented skin, hair, and eyes) is due to an enzymatic deficiency, and it is an autosomal recessive trait. Suppose that in a small country of one million people (“Generation 1”), there are 500 aa albinos and 9000 Aa heterozygous carriers. What is the probability that a child will be albino if: Both parents are members of Generation 2, and one parent is albino and the other is non-albino.

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#Question id: 4900

#Unit 8. Inheritance Biology

The chlorophyll-deficient types occur in a particular plant species due to a mutation in the DNA of the chloroplast itself, Female cytoplasm chlorophyll-deficient organisms crossed with male normal chlorophyll will produce progeny

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#Question id: 26787

#Unit 8. Inheritance Biology

In the S phase of meiotic interphase, each chromosome replicates, producing two copies of each allele, one on each chromatid, the homologous chromosomes segregation takes place in__

Which of the following statements is correct about the segregation of chromosomes?

a.If no crossing over has taken place, the two chromatids of each chromosome segregate in anaphase II and are identical

b. If crossing over has taken place, the two chromatids are no longer identical, and the different alleles segregate in anaphase II

c. If no crossing over has taken place, the two chromatids of each chromosome segregate in anaphase I and are identical