Sentence examples for share considerable overlap from inspiring English sources

Schizophrenia (SCZ) and psychotic bipolar disorder (PBD) share considerable overlap in clinical features, genetic risk factors and co-occurrence among relatives.

The pathological bases of various fibrotic diseases share considerable overlap with each other.

Although the VEGF receptors share considerable overlap in ligand binding, downstream effector interaction and biologic function, predominant actions have been identified.

Although in this paper, we have presented the various ethical challenges raised by the creation of cell lines as disconnected, they share considerable overlap.

Those enzyme activities expressed in aspen but not L. bicolor that map to biosynthesis of steroids (map00100), share considerable overlap with the pathway for synthesis of plant hormones (map01070) suggesting this observation is generally consistent with the category of plant-specific metabolism.

Unlike the heritable disorders of connective tissue with which it shares considerable overlap in manifestations, most subjects with hypermobility remain asymptomatic.

Although these two STAT proteins share considerable functional overlap, gene-disruption experiments have revealed that STAT5a and STAT5b are functionally not redundant [ 48, 49].

These findings indicate that Wolbachia two-component signaling pairs share considerable functional overlap with other α-proteobacterial systems, whereas their divergence suggests the potential for regulatory differences and cross-talk.

In addition, the phenotypic defects seen in the neurological, cardiovascular and musculoskeletal systems of ctbp2−/− embryos are worsened if they are also ctbp1−/−, indicating that the two proteins, despite having distinct roles, may share considerable functional overlap.

Dopamine and adenosine receptors are known to share a considerable overlap in their regional distribution, being especially rich in the basal ganglia.

Early onset sarcoidosis shares considerable phenotypic overlap with Blau syndrome and has also been associated with the R334W mutation in NOD2 [ 116, 146].