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Per A. Peterson

Researcher at Scripps Research Institute

Publications -  356
Citations -  36377

Per A. Peterson is an academic researcher from Scripps Research Institute. The author has contributed to research in topics: Antigen & Major histocompatibility complex. The author has an hindex of 102, co-authored 356 publications receiving 35788 citations. Previous affiliations of Per A. Peterson include General Atomics & University of Dundee.

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Independent expression of the two HL-A antigen polypeptide chains.

TL;DR: In this study support was obtained for the previous notion that the human lymphoma Daudi does not produce β2‐microglobulin (β2m), and it was apparent that these cells express the HL‐A alloantigenic polypeptide chain in amounts similar to those of other cell lines which production β2m.
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Binding of vitamin D to its human carrier plasma protein.

TL;DR: The findings suggest that vitamin D binding is associated with a conformational change in the environment of the protein bound fluorophore, and that the observed binding satisfied a mechanism of noncompetitive interaction between the protein and the two smaller molecules, TNS and vitamin D.
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Reactions and crossreactions of a rabbit anti-H2 antigen serum.

TL;DR: The F9 cell line, believed to represent cells at the morula stage, display H‐2 antigen‐like structures as revealed by the rabbit antiserum, demonstrating that there is an immunological crossreactivity between the classical alloantigenic H‐ 2 antigen chain and the alloantsigenic TL antigen chain.
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Crystallization of and preliminary X-ray data for the plasma retinol-binding protein.

TL;DR: Crystals of the human and rabbit plasma retinol-binding proteins have been grown from solutions of polyethylene glycol 6000 and CdCl2 and are in space group P212121 and have similar unit cell sizes.
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Antigen‐presenting Function of the TL Antigen and Mouse CD1 Molecules

TL;DR: The hypothesis that the TL antigen presents peptides is favored, while the data cited above do not constitute formal proof of any kind of antigen-presenting function, and it remains possible that theTL antigen does something else.