Sentence examples for both phenotypes were age from inspiring English sources

We observed two principle phenotypic differences between triple knockout males and their heterozygous siblings, and both phenotypes were age dependent.

The eight principal components described earlier were used as covariates in our bivariate GCTA analyses; as mentioned in the previous section, all phenotypes were age- and sex-regressed prior to analysis.

Continuous phenotypes were age at birth of first and last child (females only), age at menarche, age at natural menopause, length of menstrual cycle, number of live births and number of children fathered (included to test the association with male fertility).

In contrast, the dj-1β mutation produces no negative effect on development or fecundity, its only known phenotypes being age-associated loss of locomotor function and a hypersensitivity to paraquat.

Despite the appeal of the structure-led hypothesis for age-related thymic involution, our results here demonstrate that the epithelial void formation and other stromal-dependent phenotypes are aging epiphenomena, which are neither necessary nor sufficient for thymic involution to take place.

Both phenotypes were adjusted by age and sex.

Similar as in the case of mortality hazard this deleterious phenotype is age dependent occurring in middle aged and old flies but not young per mutants.

In contrast, the pulmonary fibrosis phenotype is age-dependent.

The selected phenotype variables were age, triple negative (TN) status, estrogen receptor (ER) status, progesterone receptor (PR) status, and human epidermal growth factor receptor 2 (HER2) status.

Another factor possibly influencing the endophenotypic construct – phenotype relation is age.

All ATPalpha CJ mutants exhibited 100% penetrance of this phenotype once they were aged 15 30 days post-eclosion.