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Genetic and molecular features have been recognized as useful tools to measure these risks, however, the instruments are still insufficient to design a personalized strategy for the patient.
To date, no pathological or molecular features have been found to predict for the development of invasive disease.
To date no other molecular features have been shown to differ between the bladder tumours of men and women.
As such, ecological, morphological, biochemical, and molecular features have been used over the years in attempts to classify them.
Due to challenges posed by the clonal nature of MAE, very little is known about its regulation; in particular, no molecular features have been specifically linked to MAE.
In contrast, for hundreds of other autosomal MAE genes, no molecular features have been associated with establishment and maintenance of allelic choice.
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Precise knowledge of NET biological and molecular features has opened the door to the identification of novel pharmacological targets.
Clozapine (CLZ), an antipsychotic drug currently used in the clinic but still being the object of basic studies designed to search for its unique molecular features, has been also shown to act via various heterodimers [4].
Nevertheless, to the best of our knowledge, the variable influence of PrPc expression levels according to the form of prion disease defined by its essential molecular features, has never been described and is here reported between different animals in a same transgenic mouse line.
The molecular background of the phenotypic variability in neurodegenerative dementia has been investigated and a spectrum of relations between clinical syndromes and molecular features has been identified.
The so-isolated molecular feature has been studied through its impact on adsorption extent and rate, chemical stability, calorimetric and rheological characteristics of cement paste.
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