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One to two extra hormonal stimulation cycles were initiated to obtain an accumulated minimum of 6 oocytes (group A) or alternatively of 5 embryos (group B) for each patient.
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By the values of β = 0.3 ± 0.1 and α = 0.9 ± 0.1 previously derived, the value of the dynamic scaling exponent z = α/β = 2.9 ± 0.4 (or alternatively of 1/z = 0.3 ± 0.1) is predicted.
The Sec61 translocon in yeast is composed of Sec61p, Sbh1p and Sss1p, or alternatively of Ssh1p, Sbh2p and Sss1p [ 3].
Alternatively, suppose that instead of (2′) above, we use (2″) g → OBt.
Alternatively, reduction of HIF1α levels may elicit an increase in HIF2α levels, or the regulation of the levels of HIF1α and HIF2α may be independently regulated.
Alternatively, variations of 3H activities, stable isotopes and major ions can be explained by mixing between of young recent recharge and older water stored in the catchment.
Alternatively, loss of Hos2 may promote expression of genes that inhibit morphogenesis during nitrogen starvation.
Alternatively, synthesis of ICP0 alone might be sufficient to disperse cellular microtubules.
Alternatively, association of UNG2 with centromeres during G2 might coincide with the peak in CENP-A expression [44].
Alternatively, deletion of 435 amino acids might destabilize the protein, leading to reduced or absent Asx levels within mutant clones.
Alternatively, engagement of gC1qR by sequestered parasite ligands may reduce the local availability of gC1qR for normal physiological functions, such as inhibition of the complement cascade [40].
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