HLA


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HLA

References in periodicals archive ?
HLA alleles and HLA-B27 haplotypes associated with susceptibility and severity of ankylosing spon-dylitis in a Portuguese population.
Assessment of the strength of association between HLA gene variants and disease and significant differences were determined using 95% confidence interval.
A number of HLA alleles have been investigated for its correlation among asthma, rhinitis, conjunctivitis and immunoglobulin E (IgE) levels with varying findings.
Thus, we advocate that HLA typing could be indicated at first-line to exclude CD in specific, at-risk populations such as those presenting with the autoimmune Hashimoto's disease.
HLA typing was performed using polymerase chain reaction sequence specific primer method for low resolution of HLA-A, -B, and -DR loci.
Numerous studies in the past few years have demonstrated the feasibility of HLA typing by NGS and have led to the development and availability of commercially available products on different platforms.
It would be undesirable to transmit the high loads associated with opening an exhaust valve against the high pressure of a compression release event through the HLA.
Given the need for routine HLA genotyping for histocompatibility testing, the Immunogenetics community has characterized over 14000 named HLA alleles using a variety of techniques including traditional serological approaches and more recent DNA-based methodologies including restriction fragment length polymorphism (RFLP) analysis, PCR-sequence specific oligonucleotide probes (PCR-SSOP), sequence specific primer PCR (SSP-PCR), Sanger sequence based typing (SBT) and most recently next generation sequencing (NGS) (8-19).
Pre-transplant workup done from the Apollo Main Hospitals, Chennai and their HLA typing status, pre-transplant DSA/PRA levels were collected from their serology/immunology section.
HLA genes are divided into class I (HLA-A, -C, and -B) or class ii (HLA-DR, -DQ, and -DP) genes depending on the structure and function (5).
HLA class I antigens expressed on the surface of peripheral blood lymphomononuclear cells were typed using a microlymphocytotoxity assay.
HLA typing was initially performed using serological techniques.