Literature DB >> 18760363

Emerging roles of J proteins in neurodegenerative disorders.

Sarah J Gibbs1, Janice E A Braun.   

Abstract

Several families of proteins called molecular chaperones comprise the cellular machinery that has evolved to maintain protein structure and eliminate misfolded proteins in the cell. In experimental animal models, chaperones have been shown to be powerful inhibitors of neurodegeneration. As such, molecular chaperones represent exciting pharmaceutical targets that potentially eliminate aberrant cellular proteins and slow disease progression. Current evidence indicates that the J protein family is the basis of selective chaperone action in the cell. Hence, J proteins are currently attracting attention as novel therapeutic targets for a number of neurodegenerative disorders.

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Year:  2008        PMID: 18760363     DOI: 10.1016/j.nbd.2008.07.016

Source DB:  PubMed          Journal:  Neurobiol Dis        ISSN: 0969-9961            Impact factor:   5.996


  9 in total

1.  Association of HSP70 and its co-chaperones with Alzheimer's disease.

Authors:  Linda Broer; Mohammad Arfan Ikram; Maaike Schuur; Anita L DeStefano; Joshua C Bis; Fan Liu; Fernando Rivadeneira; Andre G Uitterlinden; Alexa S Beiser; William T Longstreth; Albert Hofman; Yurii Aulchenko; Sudha Seshadri; Annette L Fitzpatrick; Ben A Oostra; Monique M B Breteler; Cornelia M van Duijn
Journal:  J Alzheimers Dis       Date:  2011       Impact factor: 4.472

2.  XPORT-dependent transport of TRP and rhodopsin.

Authors:  Erica E Rosenbaum; Kimberley S Brehm; Eva Vasiljevic; Che-Hsiung Liu; Roger C Hardie; Nansi Jo Colley
Journal:  Neuron       Date:  2011-11-17       Impact factor: 17.173

3.  Quercetin targets cysteine string protein (CSPalpha) and impairs synaptic transmission.

Authors:  Fenglian Xu; Juliane Proft; Sarah Gibbs; Bob Winkfein; Jadah N Johnson; Naweed Syed; Janice E A Braun
Journal:  PLoS One       Date:  2010-06-10       Impact factor: 3.240

Review 4.  Molecular chaperones, α-synuclein, and neurodegeneration.

Authors:  Stephan N Witt
Journal:  Mol Neurobiol       Date:  2012-08-25       Impact factor: 5.590

5.  Swa2, the yeast homolog of mammalian auxilin, is specifically required for the propagation of the prion variant [URE3-1].

Authors:  Elizabeth M Troisi; Michael E Rockman; Phil P Nguyen; Emily E Oliver; Justin K Hines
Journal:  Mol Microbiol       Date:  2015-06-25       Impact factor: 3.501

6.  Control of RUNX-induced repression of Notch signaling by MLF and its partner DnaJ-1 during Drosophila hematopoiesis.

Authors:  Marion Miller; Aichun Chen; Vanessa Gobert; Benoit Augé; Mathilde Beau; Odile Burlet-Schiltz; Marc Haenlin; Lucas Waltzer
Journal:  PLoS Genet       Date:  2017-07-25       Impact factor: 5.917

7.  Evolution of an intricate J-protein network driving protein disaggregation in eukaryotes.

Authors:  Nadinath B Nillegoda; Antonia Stank; Duccio Malinverni; Niels Alberts; Anna Szlachcic; Alessandro Barducci; Paolo De Los Rios; Rebecca C Wade; Bernd Bukau
Journal:  Elife       Date:  2017-05-15       Impact factor: 8.140

8.  KNK437 restricts the growth and metastasis of colorectal cancer via targeting DNAJA1/CDC45 axis.

Authors:  Shaoshan Yang; Xiaoli Ren; Yunshi Liang; Yongrong Yan; Yangshu Zhou; Jinlong Hu; Zhizhi Wang; Fuyao Song; Feifei Wang; Wangjun Liao; Wenting Liao; Yanqing Ding; Li Liang
Journal:  Oncogene       Date:  2019-09-02       Impact factor: 9.867

Review 9.  Emerging novel concept of chaperone therapies for protein misfolding diseases.

Authors:  Yoshiyuki Suzuki
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2014       Impact factor: 3.493

  9 in total

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