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Study Design: Mutations were studied in the following 5 groups: 47 consecutive women with preeclampsia, 49 women with preeclampsia and with hyperhomocysteinemia, 36 women with preeclampsia but without hyperhomocysteinemia, 127 women with familial preeclampsia (typed for C677T mutations only), and 120 control subjects.
Nine missense mutations were studied altogether (Figure 5C; patient genotypes are listed in the figure legend).
Exonic mutations were studied as previously described.
Epidermal growth factor receptor mutations were studied by direct sequencing.
Patients Nine families with dominant KATP channel mutations were studied.
In a report published by Rebbeck et al., 483 women with BRCA1/2 mutations were studied.
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How can such mutations be studied and their evolutionary effects understood?
However, there occurs a significant change in the degree of evolvability if the effect of accumulated mutations is studied.
The impact of these mutations was studied by measuring their effect on TERT expression, telomerase activity, and telomere length in stem cells as well as in differentiated cell types.
To determine the role of conserved amino acids in the substrate binding pocket, five single mutations and one double mutation were studied for their effects on substrate specificity.
The structural and dynamic consequences of H46A mutation were studied using multiple computational methods such as docking, molecular dynamics simulation and residue interaction network analysis (RIN).
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variants were studied
variations were studied
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transfer were studied
mutations were selected
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mutations were detected
mutations were eliminated
mutations were verified
mutations were confirmed
mutations were identified
mutations were used
mutations were genotyped
mutations were analyzed
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