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This is also consistent with previous studies (Ma et al., 2003) suggesting that a small amount of estrogen during the window of implantation is a critical determinant in specifying the duration of uterine receptivity

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Therefore, this innovative and important trial design feature has the potential to extend the use of this class of medication to those with normo- or microalbuminuriaa subgroup of patients who have yet to be included in prior key kidney protection trials

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is not readily absorbed via the GI tract, and does not affect digestion, particularly at the low levels in diet (2% or less) used in the food industry