Multicellular organism’s homeostasis and growth mainly maintained by growth factors and also tyrosine kinase receptor activity (TK). They possess extensive role in the elucidation of human cancer growth also. Cancer drugs such as Gifitinib, ematinib are the monoclonal antibodies that acts on epidermal growth factor receptors (EGFR), tyrosine kinase receptors. Inhibition of ligand dependent signaling and ligand-independent signaling of these receptors can be potentially done by these drugs.
There are characteristic dissimilarities among these even though tyrosine kinase inhibitors are analogous in that they unite within the ATP-binding region of the kinase domain.
Generally epidermal growth factor receptors kinase domain subsists in an auto-inhibited inactive conformation. Later this inactive form may take on an active conformation by asymmetric contacts through receptor dimerization.
How would you test the hypothesis that the C-terminal domain of a newly identified growth factor...
14. You are studying a newly discovered growth factor. You find that this growth factor stimulates the proliferation of cells grown in the laboratory. You have also found that the receptor that binds the growth factor is a receptor kinase that activates Ras, which activates the MAP kinase pathway. Which mutations affecting this growth factor pathway would you expect to promote uncontrolled cell proliferation? Select all that apply. A. a mutation that inactivates the phosphatase that dephosphorylates the activated receptor...
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this question has 3 parts and I need help answering them
The Epidermal Growth Factor Receptor (EGFR) is a receptor tyrosine kinase that regulates cell growth. For each of the scenarios below, explain which steps of RTK signaling would act normally and which would change. Describe what effects you would expect to observe in each cell. a. An inhibitor binds to the EGFR ligand binding site but does not induce dimerization. b. The tyrosine residues on EGFR are replaced...
2. It has been established that the so-called ‘ ZZ domain’, a synthetic IgG binding protein derived from tandem repeats of the B domain of protein A, interacts with the Fc portion of IgG molecules. HOW would you confirm that this ‘ ZZ domain’ indeed binds to the Fc region of IgG and not to that of IgM or IgE a.What would you establish as criteria for physiologically relevant binding of this ZZ domain to IgG Fc portion? b.What would...
1. What are null hypothesis and alternative hypothesis? 2. Inastatisticaltest,wehavethechoiceofatwo-tailedtest,aleft- tailed test, or a right-tailed test. Which hypothesis is the determining factor for choosing the direction of the test? (In other words, how would you decide it) 3. Forthesamesampledataandnullhypothesis,howdoesthe P-value for a two-tailed test compare to that for a one-tailed test? 4. Using P-value method, how would you reject or fail to reject the null hypothesis? (what is the decision criteria?) How does level of significance matter to the hypothesis...
How would you interpret (1-a) in the hypothesis testing framework? A)the power of a test B) the probalilitybof a type I error C)The probalility of failing to reject the null hypothsis then it is true D) the probability of Type Ii error
How would you do hypothesis test “Advil is more effective than Aleve in reduction of pain level”
Generate a hypothesis and briefly describe how you would conduct an experiment to address your hypothesis. Provide specific details such as the type of research, population, and key aspects that you would need to collect your data to test your hypothesis
How could an early stop mutation lead to an N-terminal truncated protein? What experiments would you conduct to confirm this hypothesis? (This is in regard to an article on BRCA 1 mutations, but this question is in general)
Exercise 2.2. Type the following code in your terminal. v <- factor(c("2", "3", "5", "7", "11")) a. Convert v to character with as.character. Explain what just happened. b. Convert v to numeric with as. numeric. Explain what just happened. c. How would you convert the values of v to integers?
Exercise 2.2. Type the following code in your terminal. v <- factor(c("2", "3", "5", "7", "11")) a. Convert v to character with as.character. Explain what just happened. b. Convert v to numeric with as. numeric. Explain what just happened. c. How would you convert the values of v to integers?