The peptide-binding strategy of the MHC class II I-A molecules
Immunology Today, ISSN: 0167-5699, Vol: 19, Issue: 5, Page: 212-216
1998
- 41Citations
- 15Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations41
- Citation Indexes41
- 41
- CrossRef29
- Captures15
- Readers15
- 15
Article Description
Despite the importance of murine major histocompatibility complex (MHC) class II I-A molecules for immunological research, the overall peptide-binding specificities of I-A and the homologous human HLA-DQ molecules remain unresolved. Here, Boris Reizis and colleagues review current evidence suggesting that DQ/I-A molecules bind peptides with a different hierarchy of anchor positions than has been found in the well-characterized DR/I-E proteins.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0167569997012383; http://dx.doi.org/10.1016/s0167-5699(97)01238-3; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0031780202&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/9613038; http://linkinghub.elsevier.com/retrieve/pii/S0167569997012383; http://api.elsevier.com/content/article/PII:S0167569997012383?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:S0167569997012383?httpAccept=text/plain; https://linkinghub.elsevier.com/retrieve/pii/S0167569997012383
Elsevier BV
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