Hsp70 promotes maturation of uromodulin mutants that cause familial juvenile hyperuricemic nephropathy and suppresses cellular damage

• 資料種別: 記事
• タイトル: Hsp70 promotes maturation of uromodulin mutants that cause familial juvenile hyperuricemic nephropathy and suppresses cellular damage
• 著者・編者: Sulistiyati Bayu Utami; Ryo Endo; Toshihiro Hamada
• 出版事項: 日本 : Japanese Society of Nephrology
• 出版年月日等: 2022-02-25
• 出版年（W3CDTF）: 2022-02-25
• タイトル（掲載誌）: Clinical and experimental nephrology : official publication of the Japanese Society of Nephrology
• 巻号年月日等（掲載誌）: 26(6)
• 掲載巻: 26(6)
• ISSN（掲載誌）: 1437-7799
• ISSN-L（掲載誌）: 1437-7799
• 本文の言語コード: eng
• DOI: 10.1007/s10157-022-02196-y; https://doi.org/10.1007/s10157-022-02196-y
• 国立国会図書館永続的識別子: info:ndljp/pid/12686239; https://dl.ndl.go.jp/pid/12686239
• コレクション（共通）: 障害者向け資料
• コレクション（障害者向け資料：レベル1）: テキストデータ
• コレクション（個別）: 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他; https://dl.ndl.go.jp/collections/B00035
• 収集根拠: オンライン資料収集制度
• 受理日（W3CDTF）: 2023-03-07T17:36:34+09:00
• 保存日（W3CDTF）: 2022-12-16
• 記録形式（IMT）: application/pdf
• オンライン閲覧公開範囲: 国立国会図書館内限定公開
• デジタル化資料送信: 図書館・個人送信対象外
• 遠隔複写可否（NDL）: 可
• 掲載誌（URI）: https://link.springer.com/article/10.1007/s10157-022-02196-y
• 掲載誌（国立国会図書館永続的識別子）: info:ndljp/pid/12686231; https://dl.ndl.go.jp/pid/12686231
• 連携機関・データベース: 国立国会図書館 : 国立国会図書館デジタルコレクション; https://dl.ndl.go.jp

• 要約等: コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他
• DOI: 10.1007/s10157-022-02196-y; https://doi.org/10.1007/s10157-022-02196-y
• 関連情報（URI）: http://id.ndl.go.jp/digimeta/12686239; https://dl.ndl.go.jp/pid/12686239; https://link.springer.com/content/pdf/10.1007/s10157-022-02196-y.pdf; https://link.springer.com/article/10.1007/s10157-022-02196-y/fulltext.html
• 参照: ER stress and the unfolded protein response; https://cir.nii.ac.jp/crid/1360011145585514112; Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome; https://cir.nii.ac.jp/crid/1360011146267339008; Novel missense mutation of uromodulin in mice causes renal dysfunction with alterations in urea handling, energy, and bone metabolism; https://cir.nii.ac.jp/crid/1360016869875447424; UROMODULIN Mutations Cause Familial Juvenile Hyperuricemic Nephropathy; https://cir.nii.ac.jp/crid/1360292619270503552; Endoplasmic Reticulum Stress and Oxidative Stress in Cell Fate Decision and Human Disease; https://cir.nii.ac.jp/crid/1360292621121304448; Functional stabilization of Kv1.5 protein by Hsp70 in mammalian cell lines; https://cir.nii.ac.jp/crid/1360292621257568256; Localization of the Tamm‐Horsfall glycoprotein (unomodulin) gene to chromosome 16p12.3‐16p13.11; https://cir.nii.ac.jp/crid/1360298344097811968; Uromodulin mutations causing familial juvenile hyperuricaemic nephropathy lead to protein maturation defects and retention in the endoplasmic reticulum; https://cir.nii.ac.jp/crid/1360574095915125760; Endoplasmic Reticulum Stress in UMOD-Related Kidney Disease: A Human Pathologic Study; https://cir.nii.ac.jp/crid/1360579815842001920; Activation of HSP70 impedes tert-butyl hydroperoxide (t-BHP)-induced apoptosis and senescence of human nucleus pulposus stem cells via inhibiting the JNK/c-Jun pathway; https://cir.nii.ac.jp/crid/1360579817462268928; Transcriptional activation of the anchoring protein SAP97 by heat shock factor (HSF)‐1 stabilizes K_v1.5 channels in HL‐1 cells; https://cir.nii.ac.jp/crid/1361137044397717632; Identification of Human Uromodulin as the Tamm-Horsfall Urinary Glycoprotein; https://cir.nii.ac.jp/crid/1361418519247301248; Intracellular transport, cell-surface exposure and release of recombinant Tamm-Horsfall glycoprotein; https://cir.nii.ac.jp/crid/1361699994683411328; Protein Oligomerization in the Endoplasmic Reticulum; https://cir.nii.ac.jp/crid/1361981468408394240; Mutant Tamm-Horsfall Glycoprotein Accumulation in Endoplasmic Reticulum Induces Apoptosis Reversed by Colchicine and Sodium 4-Phenylbutyrate; https://cir.nii.ac.jp/crid/1361981468459677952; Identification and characterization of D8C, a novel domain present in liver‐specific LZP, uromodulin and glycoprotein 2, mutated in familial juvenile hyperuricaemic nephropathy; https://cir.nii.ac.jp/crid/1361981469833932800; Defective Intracellular Trafficking of Uromodulin Mutant Isoforms; https://cir.nii.ac.jp/crid/1361981471078920192; Heat Shock Proteins 27 and 70: Anti-Apoptotic Proteins with Tumorigenic Properties; https://cir.nii.ac.jp/crid/1362262944880081024; Biochemical and Mechanical Dysfunction in a Mouse Model of Desmin-Related Myopathy; https://cir.nii.ac.jp/crid/1362262946288281728; Uromodulin storage disease; https://cir.nii.ac.jp/crid/1363107371356246016; Ubiquitin-Proteasome System Impairment Caused by a Missense Cardiac Myosin-binding Protein C Mutation and Associated with Cardiac Dysfunction in Hypertrophic Cardiomyopathy; https://cir.nii.ac.jp/crid/1363388845208220416; Molecular and Cellular Effects of Tamm-Horsfall Protein Mutations and Their Rescue by Chemical Chaperones; https://cir.nii.ac.jp/crid/1363388845234101504; Induction of HSP70 promotes ΔF508 CFTR trafficking; https://cir.nii.ac.jp/crid/1363670318607705088; Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics; https://cir.nii.ac.jp/crid/1363951794870951424; Tamm–Horsfall protein or uromodulin: new ideas about an old molecule; https://cir.nii.ac.jp/crid/1363951796011876352; Reciprocal Control of hERG Stability by Hsp70 and Hsc70 with Implication for Restoration of LQT2 Mutant Stability; https://cir.nii.ac.jp/crid/1390001205246172416; Apoptosis induced by an uromodulin mutant C112Y and its suppression by topiroxostat; https://cir.nii.ac.jp/crid/2051433317027809536
• 連携機関・データベース: 国立情報学研究所 : CiNii Research; https://cir.nii.ac.jp/
• 提供元機関・データベース: 雑誌記事索引データベース; https://ndlsearch.ndl.go.jp; Crossref; https://www.crossref.org; 科学研究費助成事業データベース; https://kaken.nii.ac.jp/ja
• 書誌ID（NDLBibID）: 12686239; http://id.ndl.go.jp/bib/12686239