Following statements are regarding to the heat production by the activation of sympathetic nervous system.

A. Activation is stimulation of β receptors in brown fat, which increases metabolic rate and heat production.

B. Activation is stimulation of α2 receptors in brown fat, which increases metabolic rate and heat production.

C. Stimulation of α1 receptors in vascular smooth muscle of skin blood vessels, producing vasoconstriction. Vasoconstriction reduces blood flow to the surface of the skin.

D. Stimulation of α1 receptors in vascular smooth muscle of skin blood vessels, producing vasodilation. Vasodilation reduces blood flow to the surface of the skin.

Which of the following combination is correct?

TLS Online TPP Program

#Question id: 12499

#Unit 8. Inheritance Biology

On the basis of the linked marker genotypes II 3 can be told that:

TLS Online TPP Program

#Question id: 12500

#Unit 8. Inheritance Biology

In this pedigree II 1 is affected with an autosomal recessive disorder. The disease status for II 2, II 3 and II 4 is unknown. A and B represent alleles at a locus which is tightly linked to the disease locus with recombination fraction of 0. On the basis of the linked markers II 2 can be told that: 

TLS Online TPP Program

#Question id: 12501

#Unit 8. Inheritance Biology

In the pedigree shown, on the basis of the linked marker results II 3 can be told that:

TLS Online TPP Program

#Question id: 12502

#Unit 8. Inheritance Biology

In the pedigree shown, on the basis of the linked marker results II 4 can be told that:

TLS Online TPP Program

#Question id: 12503

#Unit 8. Inheritance Biology

In this pedigree II 1 is affected with an autosomal recessive disorder. The disease status for II 2 is unknown. A and B represent alleles at a locus which is tightly linked to the disease locus with recombination fraction of 0. Using the linked markers, II2 can be told that:

TLS Online TPP Program

#Question id: 12504

#Unit 8. Inheritance Biology

In this pedigree II 3 and III 1 are affected with an X-linked recessive disorder which is tightly linked to a marker locus with alleles A and B, with a recombination fraction of 0 between the disease and marker loci. Analysis of the linked marker results indicates that the disease must be segregating with: