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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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Biomagnetic isolation of antigen-specific CD8+ T cells usable in immunotherapy

TL;DR: Following isolation and expansion of antigen-specific CD8+ T lymphocytes from mixed T-cell populations, recovered cells specifically killed target cells in vitro and displayed antiviral effect in vivo.
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Quantitation of peptide anchor residue contributions to class I major histocompatibility complex molecule binding.

TL;DR: Compared the affinities of various octapeptides for purified, soluble H-2Kb molecules revealed that at least 2 anchor residues are necessary for high-affinity binding, and that high-Affinity binding occurs only when anchor side chains are optimally packed within the groove.
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Urinary Immunoglobulin Components in Normal, Tubular, and Glomerular Proteinuria: Quantities and Characteristics of Free Light Chains, IgG, IgA, and Fcγ Fragment.

TL;DR: The results indicate an excess normal production of light chains in the patients with tubular proteinuria, assuming that all or most of the free chains originate from de novo synthesis.
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Structural and functional studies of vitamin a-binding proteins*

TL;DR: Details of the transport system for vitamin A were elucidated in any detail, including the determination of the primary structure of prealbumin, the protein which forms a complex with RBP in plasma, and the elucidation of the tertiary structure ofPrealbumin.
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Plasma vitamin A transport and visual dark adaptation in diseases of the intestine and liver.

TL;DR: Only at RBP concentrations below half the normal was impairment of the dark adaptation observed, suggesting that serum RBP is a more sensitive indicator of vitamin A deficiency than measurement of dark adaptation.