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#Question id: 4767
#SCPH12 I Genetics
Neurofibromatosis is a condition in humans which is generally inherited in a dominant fashion. Assuming this disorder is 90% penetrant, what is the chance that a single child born to a father with neurofibromatosis and a mother known not to carry the mutation will have the disorder?
TLS Online TPP Program
#Question id: 14090
#SCPH05 I Biotechnology
Which of the following is an example of a primary protein sequence database?
TLS Online TPP Program
#Question id: 16125
#SCPH01 Biochemistry
You are studying regulation of the yeast enzyme glutamine synthetase (GS), which is encoded by the GLN1 gene. You have isolated two mutants, designated gln2– and gln3–, that give decreased GS activity. Mating of either gln2– or gln3– haploids to wild type produces heterozygous diploids that show normal amounts of GS expression. When you cross either a gln2– or gln3– haploid to a gln1– strain the resulting diploids show normal expression of GS.
From these experiments, Classify the gln2– and gln3– mutations in terms of their basic genetic properties explaining the rationale behind your conclusions. Based on these properties make a proposal for the types of regulatory functions affected by the gln2– and gln3– mutations.
TLS Online TPP Program
#Question id: 1103
#SCPH01 Biochemistry
An inhibitor of which of the following enzymes could be used to block the release of calcium from the endoplasmic reticulum?
TLS Online TPP Program
#Question id: 15478
#SCPH06 I Botany
Escherichia coli preferentially utilizes glucose by preventing the uptake of lactose and switching off transcription of the lac operon. This mechanism is known as