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Journal Abstract Search

180 related items for PubMed ID: 29317501

  • 1. Most mutations that cause spinocerebellar ataxia autosomal recessive type 16 (SCAR16) destabilize the protein quality-control E3 ligase CHIP.
    Kanack AJ, Newsom OJ, Scaglione KM.
    J Biol Chem; 2018 Feb 23; 293(8):2735-2743. PubMed ID: 29317501
    [Abstract] [Full Text] [Related]

  • 2. Disrupted structure and aberrant function of CHIP mediates the loss of motor and cognitive function in preclinical models of SCAR16.
    Shi CH, Rubel C, Soss SE, Sanchez-Hodge R, Zhang S, Madrigal SC, Ravi S, McDonough H, Page RC, Chazin WJ, Patterson C, Mao CY, Willis MS, Luo HY, Li YS, Stevens DA, Tang MB, Du P, Wang YH, Hu ZW, Xu YM, Schisler JC.
    PLoS Genet; 2018 Sep 23; 14(9):e1007664. PubMed ID: 30222779
    [Abstract] [Full Text] [Related]

  • 3. In vitro characterization of six STUB1 variants in spinocerebellar ataxia 16 reveals altered structural properties for the encoded CHIP proteins.
    Pakdaman Y, Sanchez-Guixé M, Kleppe R, Erdal S, Bustad HJ, Bjørkhaug L, Haugarvoll K, Tzoulis C, Heimdal K, Knappskog PM, Johansson S, Aukrust I.
    Biosci Rep; 2017 Apr 30; 37(2):. PubMed ID: 28396517
    [Abstract] [Full Text] [Related]

  • 4. The molecular basis of spinocerebellar ataxia type 48 caused by a de novo mutation in the ubiquitin ligase CHIP.
    Umano A, Fang K, Qu Z, Scaglione JB, Altinok S, Treadway CJ, Wick ET, Paulakonis E, Karunanayake C, Chou S, Bardakjian TM, Gonzalez-Alegre P, Page RC, Schisler JC, Brown NG, Yan D, Scaglione KM.
    J Biol Chem; 2022 May 30; 298(5):101899. PubMed ID: 35398354
    [Abstract] [Full Text] [Related]

  • 5. Genetic Dominant Variants in STUB1, Segregating in Families with SCA48, Display In Vitro Functional Impairments Indistinctive from Recessive Variants Associated with SCAR16.
    Pakdaman Y, Berland S, Bustad HJ, Erdal S, Thompson BA, James PA, Power KN, Ellingsen S, Krooni M, Berge LI, Sexton A, Bindoff LA, Knappskog PM, Johansson S, Aukrust I.
    Int J Mol Sci; 2021 May 30; 22(11):. PubMed ID: 34070858
    [Abstract] [Full Text] [Related]

  • 6. Changes in protein function underlie the disease spectrum in patients with CHIP mutations.
    Madrigal SC, McNeil Z, Sanchez-Hodge R, Shi CH, Patterson C, Scaglione KM, Schisler JC.
    J Biol Chem; 2019 Dec 13; 294(50):19236-19245. PubMed ID: 31619515
    [Abstract] [Full Text] [Related]

  • 7. Clinical and Genetic Characterization of Autosomal Recessive Spinocerebellar Ataxia Type 16 (SCAR16) in Taiwan.
    Chiu HH, Hsaio CT, Tsai YS, Liao YC, Lee YC, Soong BW.
    Cerebellum; 2020 Aug 13; 19(4):544-549. PubMed ID: 32367277
    [Abstract] [Full Text] [Related]

  • 8. CHIP mutations affect the heat shock response differently in human fibroblasts and iPSC-derived neurons.
    Schuster S, Heuten E, Velic A, Admard J, Synofzik M, Ossowski S, Macek B, Hauser S, Schöls L.
    Dis Model Mech; 2020 Oct 12; 13(10):. PubMed ID: 33097556
    [Abstract] [Full Text] [Related]

  • 9. Spinocerebellar ataxia type 48: last but not least.
    De Michele G, Galatolo D, Barghigiani M, Dello Iacovo D, Trovato R, Tessa A, Salvatore E, Filla A, De Michele G, Santorelli FM.
    Neurol Sci; 2020 Sep 12; 41(9):2423-2432. PubMed ID: 32342324
    [Abstract] [Full Text] [Related]

  • 10. Biochemical and Proteomic Analysis of Ubiquitination of Hsc70 and Hsp70 by the E3 Ligase CHIP.
    Soss SE, Rose KL, Hill S, Jouan S, Chazin WJ.
    PLoS One; 2015 Sep 12; 10(5):e0128240. PubMed ID: 26010904
    [Abstract] [Full Text] [Related]

  • 11. Ataxia and hypogonadism caused by the loss of ubiquitin ligase activity of the U box protein CHIP.
    Shi CH, Schisler JC, Rubel CE, Tan S, Song B, McDonough H, Xu L, Portbury AL, Mao CY, True C, Wang RH, Wang QZ, Sun SL, Seminara SB, Patterson C, Xu YM.
    Hum Mol Genet; 2014 Feb 15; 23(4):1013-24. PubMed ID: 24113144
    [Abstract] [Full Text] [Related]

  • 12. Endoplasmic reticulum protein quality control is determined by cooperative interactions between Hsp/c70 protein and the CHIP E3 ligase.
    Matsumura Y, Sakai J, Skach WR.
    J Biol Chem; 2013 Oct 25; 288(43):31069-79. PubMed ID: 23990462
    [Abstract] [Full Text] [Related]

  • 13. Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48).
    Chen HY, Hsu CL, Lin HY, Lin YF, Tsai SF, Ho YJ, Li YR, Tsai JW, Teng SC, Lin CH.
    J Biomed Sci; 2021 Sep 26; 28(1):65. PubMed ID: 34565360
    [Abstract] [Full Text] [Related]

  • 14. CHIP protects from the neurotoxicity of expanded and wild-type ataxin-1 and promotes their ubiquitination and degradation.
    Al-Ramahi I, Lam YC, Chen HK, de Gouyon B, Zhang M, Pérez AM, Branco J, de Haro M, Patterson C, Zoghbi HY, Botas J.
    J Biol Chem; 2006 Sep 08; 281(36):26714-24. PubMed ID: 16831871
    [Abstract] [Full Text] [Related]

  • 15. Disease-associated mutations in C-terminus of HSP70 interacting protein (CHIP) impair its ability to negatively regulate mitophagy.
    Earnshaw R, Zhang YT, Heymann G, Fujisawa K, Hui S, Kapadia M, Kalia LV, Kalia SK.
    Neurobiol Dis; 2024 Oct 01; 200():106625. PubMed ID: 39117117
    [Abstract] [Full Text] [Related]

  • 16. Chip Protein U-Box Domain Truncation Affects Purkinje Neuron Morphology and Leads to Behavioral Changes in Zebrafish.
    Pakdaman Y, Denker E, Austad E, Norton WHJ, Rolfsnes HO, Bindoff LA, Tzoulis C, Aukrust I, Knappskog PM, Johansson S, Ellingsen S.
    Front Mol Neurosci; 2021 Oct 01; 14():723912. PubMed ID: 34630034
    [Abstract] [Full Text] [Related]

  • 17. Spinocerebellar ataxia type 17-digenic TBP/STUB1 disease: neuropathologic features of an autopsied patient.
    Saito R, Tada Y, Oikawa D, Sato Y, Seto M, Satoh A, Kume K, Ueki N, Nakashima M, Hayashi S, Toyoshima Y, Tokunaga F, Kawakami H, Kakita A.
    Acta Neuropathol Commun; 2022 Dec 07; 10(1):177. PubMed ID: 36476347
    [Abstract] [Full Text] [Related]

  • 18. The E3 ubiquitin ligase CHIP selectively regulates mutant epidermal growth factor receptor by ubiquitination and degradation.
    Chung C, Yoo G, Kim T, Lee D, Lee CS, Cha HR, Park YH, Moon JY, Jung SS, Kim JO, Lee JC, Kim SY, Park HS, Park M, Park DI, Lim DS, Jang KW, Lee JE.
    Biochem Biophys Res Commun; 2016 Oct 14; 479(2):152-158. PubMed ID: 27475501
    [Abstract] [Full Text] [Related]

  • 19. Feedback inhibition of cAMP effector signaling by a chaperone-assisted ubiquitin system.
    Rinaldi L, Delle Donne R, Catalanotti B, Torres-Quesada O, Enzler F, Moraca F, Nisticò R, Chiuso F, Piccinin S, Bachmann V, Lindner HH, Garbi C, Scorziello A, Russo NA, Synofzik M, Stelzl U, Annunziato L, Stefan E, Feliciello A.
    Nat Commun; 2019 Jun 12; 10(1):2572. PubMed ID: 31189917
    [Abstract] [Full Text] [Related]

  • 20. LRSAM1 E3 ubiquitin ligase: molecular neurobiological perspectives linked with brain diseases.
    Mishra R, Upadhyay A, Prajapati VK, Dhiman R, Poluri KM, Jana NR, Mishra A.
    Cell Mol Life Sci; 2019 Jun 12; 76(11):2093-2110. PubMed ID: 30826859
    [Abstract] [Full Text] [Related]

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