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In the first analysis we studied A content in all genes in the genome.
In this current analysis, we studied a subset of these subjects for whom longitudinal data was available.
In our analysis we studied a total of 288 spectra (encompassing approximately 85% of total BV-BJ rearrangements), each exhibiting 8 to 10 peaks.
In the current analysis, we studied a panel of nine genetic polymorphisms within seven genes (TS, MTHFR, GSTP1, GSTT1, GSTM1, ERCC1, ERCC2) involved in the metabolism of cisplatin and 5-FU as well as genes of the NER.
However, the facility-based survey in India and case-control study in Nepal compared kala-azar patients to the general population, whereas in the current analysis we studied a relatively homogeneous, high-risk population.
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In a separate analysis, we studied whether the duration of a woman's first pregnancy was associated with breast cancer risk, stratified by whether PE/HIP occurred or not in the first pregnancy.
In a sensitivity analysis, we studied whether ethnic variation showed clustering at a hospital level, which may indicate influence of hospital-service characteristics.
Using survival analysis, we studied medical history data from a prospective cohort of HTLV-I– and HTLV-II infected and –uninfected blood donors, all HTLV-II infected.
To better document these issues and to demonstrate the utility of such an analysis, we studied the Wabash River Watershed located in the U.S. Midwest.
Hence, in a second analysis we studied each ecosystem independently.
Since these approaches do not allow a quantitative analysis we studied the seroreactivity of GLEA2 by ELISA.
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