Sentence examples for more frequent subtypes from inspiring English sources

Kappa statistics were highest for the more frequent subtypes of SVO (0.97) and CH (0.97).

Genetic heterogeneity complicates genetic counseling, since information concerning the more frequent subtypes cannot be extrapolated to rarer forms of the disease.

This, together with the lack of phase III studies in the more frequent subtypes such as GIST, leaves us with the conclusion that sorafenib has not yet a clearly defined role in the treatment of sarcoma.

The more frequent subtypes (BVDV-1b and 1e) were distributed across the entire country, whereas the less frequent subtypes (BVDV-1a, d, g, h, and k) were present in two or three macroareas, except for BVDV-1f, which was limited to the North (Table 1 and Figure 2).

In contrast to what was observed in the mouse groups, human tumors on average demonstrated more frequent subtype-specific regions of copy number loss compared to copy number gains (Supplemental Table 5).

Of note, the thymidine analogue mutations M41L, L210W and the 3TC-associated mutation M184V/I, as well as the PI mutation L90M, were significantly more frequent in subtype B isolates (p<0.05, data not shown).

To evaluate whether p-alpha-synuclein deposits were more frequent in certain subtypes of nerve fibers, we performed double immunostaining of for p-alpha-synuclein with SP, CGRP, VIP and TH in all p-alpha-synuclein-positive cases (Fig.  2).

In a Ugandan study [ 6], the K103N mutation was relatively more frequent in C subtype- infected women failing NNRTI-based therapy than in both A and D subtypes.

I222V, H274Y and N294S were found in a higher number in the N1 subtype, while E119G/A/D was more frequent in the N2 subtype.

There was a greater percent of the Combined subtype (ADDC) (59.4%), than Inattentive subtype (ADDI) (31.0%) which also was more frequent than the Hyperactive subtype (ADDH) (9.1%).

Mutations in KIT are more frequent in specific melanoma subtypes, and response to KIT inhibition is likely to depend on the identified mutation.