Sentence examples for variations that seem from inspiring English sources

Exact(5)

He can take apart Poussin's The Triumph of Pan, reconfiguring the elements of its composition over and again in semi-abstract variations that seem to unleash the intensely structured violence of the original.

When both members of a pair had taken cannabis, which was true for 445 of them, their average score jumped to +0.12.Together, these findings suggest that people born with a lot of the genetic variations that seem to predispose to schizophrenia are more likely to take cannabis than those born with few of them.

LEMS may also be associated with autoimmune diseases, such as hypothyroidism (an underactive thyroid gland) or diabetes mellitus type 1. Myasthenia gravis, too, may happen in the presence of tumors (thymoma, a tumor of the thymus in the chest); people with MG without a tumor and people with LEMS without a tumor have similar genetic variations that seem to predispose them to these diseases.

In the study we found a significant effect of allelic predisposition for the disease as well as variations that seem to have a protective effect against the disease.

One approach to identifying the causes of alcoholism, particularly without crossing ethical boundaries in human subjects, is to look at the person's genome (and particularly at the variations that naturally arise in the DNA) to identify those variations that seem to be found more commonly in people with the disease.

Similar(55)

Yet some of the dishes, especially the salads, offered variations that seemed so subtle they hardly merited separate recipes.

Standard cultural evolution models, from the very beginning, have contained transformative processes such as guided variation, that seem to us to be identical to narrow cultural attraction.

While using the same data and econometric specifications, our findings vary greatly across these subgroups, and it is this variation that seems to explain the heterogeneity of results in the literature.

Partial CNDI in the Swedish family is caused by an AQP2 variation that seems to disable the encoded AQP2-R254W protoin to reach the subapical vesicle population as well as impairing its phosphorylation at S256.

In contrast, the more consistent divergence time estimate inferred from the Y-chromosome data (t~2000 years; Table 4) may be related to the erasure of previous ancestral variation that seems to have caused the current predominance of haplogroup E3a-M2, leading to a better fitting of the Y-chromosome data to the model.

Scientists from the University of British Columbia have identified a genetic variation, called the ADRA2b-deletion variant, that seems to be linked with focusing on the negative.

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