TLS Online TPP Program

#Question id: 5726


Following diagram represents the sequence of genes in a normal chromosome of a plant species

CORRECT combination for chromosomal mutation using

#Unit 8. Inheritance Biology
  1. A: Duplication      B: Pericentric inversion  C: Translocation 

  2. A: Reciprocal translocation   B: Pericentric inversion  C: Tendem duplication

  3. A: Nonreciprocal translocation   B: paracentric inversion  C: Tendem duplication

  4. A: Nonreciprocal translocation   B: Pericentric inversion  C: Tendem duplication

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TLS Online TPP Program

#Question id: 12241

#Unit 10. Ecological Principles

The process of speciation can be prevented by

TLS Online TPP Program

#Question id: 6992

#Unit 5. Developmental Biology

Epimorphosis is regeneration through:

TLS Online TPP Program

#Question id: 12181

#Unit 2. Cellular Organization

Following statements are regarding to the CFTR.
A. cystic fibrosis transmembrane conductance regulator allows Cl− ions to flow out of the cell, following their concentration gradient.
B. ATP binding to CFTR’s two nucleotide-binding domains appears to close the Cl− channel, and the hydrolysis of one ATP opens it (the other ATP remains intact).
C. the CFTR channel can open only if its regulatory domain (which is unique among ABC transporters) has been phosphorylated, thus regulating the flow of ions across the membrane.
D. The maintenance of electrical neutrality requires that the Cl− ions transported by the CFTR be accompanied by positively charged ions, mainly Na+. The transported ions are osmotically accompanied by water, thus maintaining the proper level of fluidity in secretions of the airways, intestinal tract, and the ducts of the pancreas, testes, and sweat glands.
Which of the following combination is correct?

TLS Online TPP Program

#Question id: 15258

#Unit 2. Cellular Organization

Complex media contain components like 

TLS Online TPP Program

#Question id: 4110

#Unit 3. Fundamental Processes

Tay-Sachs disease belongs to the family of lysosomal storage diseases; it is an autosomal recessive neurodegenerative disorder caused by deficiency of the lysosomal enzyme hexosaminidase. The inability to degrade sphingolipids results in the deposition of these lipids in the cells that causes severe mental retardation and death in childhood. The most common mutation in Tay-Sachs disease patients is a 4-base pair insertion in exon 11 of the 14 exons of the hexosaminidase gene. What could be the most likely consequence of this mutation?