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Roger M. Perlmutter

Researcher at University of Washington

Publications -  81
Citations -  10244

Roger M. Perlmutter is an academic researcher from University of Washington. The author has contributed to research in topics: T-cell receptor & T cell. The author has an hindex of 47, co-authored 80 publications receiving 10125 citations. Previous affiliations of Roger M. Perlmutter include Merck & Co. & Howard Hughes Medical Institute.

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A Syndrome of Multiorgan Hyperplasia with Features of Gigantism, Tumorigenesis, and Female Sterility in p27Kip1-Deficient Mice

TL;DR: P27 deficiency may cause a cell-autonomous defect resulting in enhanced proliferation in response to mitogens, and in the spleen, the absence of p27 selectively enhanced proliferation of hematopoietic progenitor cells.
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Interaction of the unique N-terminal region of tyrosine kinase p56lck with cytoplasmic domains of CD4 and CD8 is mediated by cysteine motifs

TL;DR: The results suggest a novel role for cysteine-mediated interactions between unrelated proteins and provide a model for the association of other src-like cytoplasmic kinases with transmembrane proteins.
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Defective T cell receptor signaling in mice lacking the thymic isoform of p59fyn

TL;DR: Data confirm that p59fynT plays a pivotal role in TCR signal transduction and demonstrate that additional developmentally regulated signaling components also contribute to TCR-induced lymphocyte activation.
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A lymphocyte-specific protein-tyrosine kinase gene is rearranged and overexpressed in the murine T cell lymphoma LSTRA

TL;DR: It is inferred that the lskT-encoded protein-tyrosine kinase may aid in transducing proliferative or differentiative signals unique to lymphocytes in order to mediate neoplastic transformation in lymphocytes.
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Selective requirement for MAP kinase activation in thymocyte differentiation.

TL;DR: The results indicate that the intracellular signals regulating lineage commitment in T cells parallel those in photo-receptor cell specification in Drosophila and vulval cell differentiation in Caenorhabditis elegans suggesting that general rules for cell-type specification could apply among all metazoans.