C4BCanterbury 4 Business (Kent, England, UK)
C4BComputers for Business
C4BConsulting 4 Business
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References in periodicals archive ?
Subjects with heterozygous deletions of CYP21 and the neighboring C4B gene were identified by Southern analysis using TagI- and KpnI-restricted DNA probed with a 21-hydroxylase probe essentially as described previously (12).
Commonly, gene deletions are generated by unequal crossing over during meiosis, which produces a deletion of a 30-kb fragment, including the 3' end of CYP21P, the C4B gene, and the 5' end of CYP21 (8).
With its Unified Communications software XPhone Connect, C4B offers a solution that includes a central directory service and an app that gives employees flexible access to company contacts.
The regulators bind C3b (and C4b) and increase its decay or proteolysis from the C3 and C5 convertases of the classical and alternative pathways.
Boon et al., "Genomic copy number variations of the complement component C4B gene are associated with chronic central serous chorioretinopathy," Investigative Ophthalmology & Visual Science, vol.
No biomarkers are available for this pathology and, to the best of our knowledge, only a comparative proteomic study on plasma samples from 24 pooled MVP patients with moderate to severe MR revealed reduced levels of haptoglobin, platelet basic protein, and complement component C4b in the MVP/MR patients as compared to the 24 pooled matched control cases [16].
C4B: SI 2 sts to cable needle and hold in back, k2, k2 from cable needle.
Low levels of immunoglobulins found to correlate with more aberrant behaviors.13 A low level of IgA also has been observed in autistic patients which results in immunodeficiency.14 It is suggested that IgA deficiency has been associated with inheritance of C4B null allele (no C4B protein is produced).
They inhibit activation by binding to C3b and C4b in the complement system.