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This accordance is explained by the inherent involvement of the morphometric features in the growing process.
We conducted a case-control study to evaluate nuclear morphometric features in benign breast tissue in association with subsequent breast cancer risk.
Actually, the literature does not discuss the statistical aspects of the morphometric features in fibroblast evolution relative to this class organization.
To date, only one study has been published that assessed morphometric features in association with subsequent development of breast cancer among women with BBD [ 16].
Acta1 is developmentally regulated and associated with morphometric features in mouse [ 44] and the promoters associated with both Acta1 and ERα show tissue specific DNA methylation heterogeneity [ 45, 46].
Here we present a retrospective analysis of clinical, neuropsychological and neuroimaging (volumetric and voxel-based morphometric) features in a pathologically ascertained cohort of 95 cases of frontotemporal lobar degeneration classified according to contemporary neuropathological criteria.
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Certain nuclear morphometric features measured in breast tumor tissue have been shown to predict the prognosis of breast cancer patients.
Indeed, certain nuclear morphometric features measured in breast tumor tissue have been shown to predict the prognosis of breast cancer patients [ 11– 15].
Persistent differences in specific lung morphometric features were observed in respect to normoxia versus hyperoxia.
In the study reported here, we conducted a nested case-control study to evaluate whether nuclear morphometric features as evaluated in tissue sections of BBD may be related to the risk of subsequent breast cancer among patients with BBD.
In a case control-blinded case control-blinded et al. [22] studied the morphometricomparison of the Mehassebum in uteti from pre- ald postmenopausal women with and without uterine adenomyosis as the sole pathology.
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