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First, what is the mechanistic basis for the defect observed in Pol II CTD phosphorylation cycling and is this the direct cause of increased transcription observed in the RNF20 depleted cell line?
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The subtle differences that have been uncovered between Sar1A and Sar1B in these studies might also provide an explanation for the molecular basis of the defect in CMRD.
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Both the experimental and the numerical results were in good agreement with predictions according to the R6 method and provided a basis for the engineering defect assessment of brazed components based on failure assessment diagrams.
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Without excluding the involvement of secondary histological alterations, the data presented in this work provide a cellular basis for the neuropsychiatric defects induced by prenatal inflammation.
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