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Yuko Yamanaka

Researcher at Yokohama City University

Publications -  11
Citations -  330

Yuko Yamanaka is an academic researcher from Yokohama City University. The author has contributed to research in topics: Signal transducing adaptor protein & Induced pluripotent stem cell. The author has an hindex of 9, co-authored 11 publications receiving 313 citations. Previous affiliations of Yuko Yamanaka include Kihara Institute for Biological Research.

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Contribution of lysine 11-linked ubiquitination to MIR2-mediated major histocompatibility complex class I internalization.

TL;DR: It is shown that the polyubiquitin chain generated by the viral E3 ubiquitin ligase of Kaposi sarcoma-associated herpesvirus, MIR2, is a Lys11 and Lys63 mixed-linkage chain that can function as an internalization signal for major histocompatibility complex class I (MHC I) membrane proteins in vivo.
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Characterization of receptor proteins using affinity cross-linking with biotinylated ligands

TL;DR: This work successfully applied the use of affinity cross-linking of biotinylated ligands for a ligand-based survey of the corresponding receptor molecules and demonstrates the applicability of this method to the purification and identification of plant receptor proteins.
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Characterization of multiple alternative forms of heterogeneous nuclear ribonucleoprotein K by phosphate-affinity electrophoresis.

TL;DR: The results indicated that the multiple forms of hnRNP K were differentially modulated in response to external stimulation with bacterial lipopolysaccharide or serum, and the subcellular localization of these proteins revealed by the 2‐D gel correlated with their phosphorylation states and alternative splicing patterns.
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Proteomic analysis of membrane proteins expressed specifically in pluripotent murine embryonic stem cells.

TL;DR: To identify membrane proteins that are involved in the regulation of pluripotent stem cells, the membrane proteins of murine ESCs cultured with or without leukemia inhibitory factor (LIF) were purified and analyzed by quantitative proteomics.