Sentence examples for a deficient type from inspiring English sources

Exact(1)

Subjects with asthma have increased susceptibility to RV infections, and a deficient type 1 antiviral immune response has been suggested as one of the mechanisms involved in RV-induced asthma exacerbations.

Similar(59)

There are four subtypes of Sanfilippo disease: type A – sulfamidase deficient; type B – α-N-acetylglucosaminidase deficient; type C – acetyl-CoA: α-N-glucosaminide transferase deficient; type D – glucosamine-6-sulfatase deficient.

Table 1 (A) is for a wild-type injury and (B) is for an FVII deficient type injury.

There was no discernible difference detected in endothelial cell staining by FPL in α-Gal A deficient vs. wild-type mouse brain (indicated by green arrowheads in cerebellum, Figure  3b, f).

Table 1 compares the volume sizes of the clot components in two -stacks, one for a typical wild-type injury and the other for a typical FVII deficient type injury (here,, e.g., means the red channel value and green channel value of a voxel are both above their corresponding thresholds, and the blue channel value is below its threshold).

By continuous immersion in classical SBF for 7 days, the coating transformed into pure calcium deficient type B carbonate apatite with nano-crystallinity, which was similar to biological apatite.

Insulin deficient type 1 diabetes exhibits increased expression of NPY and hyperphagia [ 18].

These findings suggest that the dry eye present in this patient is typically of the aqueous deficient type.

Insulin deficient type 1 diabetes exhibits hyperphagia and is associated with increased expression of NPY in ARC [ 18].

RDEB is characterised by an extremely severe blistering due to poor adherence of epidermis to the dermis caused by deficient type VII collagen (COLVII), the major component of the anchoring fibrils (Bruckner-Tuderman et al, 1999; Fine et al, 2008).

Some mutations (type 1 mutations) are associated with quantitative deficiency in CFH (decreased plasma levels), but many are associated with normal plasma levels of CFH, the mutant CFH being functionally deficient (type 2 mutations) [ 2].

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