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Positions, Beliefs and Values.indd
Positions, Beliefs and Values.indd

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... obstructive pulmonary disease. Patients with cystic fibrosis and homozygosity for the common phe508del mutation had an increased risk of severe pulmonary disease if they are also homozygous for C at nucleotide 29 of the TGFB1 gene, corresponding to a change in codon 10 (Drumm et al., 2005). High TGF ...
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Transcription
Transcription

... Brings proteins binding to the promoter into closer proximity In some complexes, TBP is present but does not bind DNA ...
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Point mutation



A point mutation, or single base modification, is a type of mutation that causes a single nucleotide base change, insertion, or deletion of the genetic material, DNA or RNA. The term frameshift mutation indicates the addition or deletion of a base pair. A point mutant is an individual that is affected by a point mutation.Repeat induced point mutations are recurring point mutations, discussed below.
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