Literature DB >> 27191645

Proteostasis: Chaperoning for hearing loss.

Gergely L Lukacs1.   

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Year:  2016        PMID： 27191645     DOI： 10.1038/nchembio.2091

Source DB:  PubMed          Journal:  Nat Chem Biol        ISSN： 1552-4450            Impact factor:   15.040


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  10 in total

Review 1.  Structures of usher syndrome 1 proteins and their complexes.

Authors:  Lifeng Pan; Mingjie Zhang
Journal:  Physiology (Bethesda)       Date:  2012-02

Review 2.  Protein homeostasis at the plasma membrane.

Authors:  Pirjo M Apaja; Gergely L Lukacs
Journal:  Physiology (Bethesda)       Date:  2014-07

3.  A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.

Authors:  E Verpy; M Leibovici; I Zwaenepoel; X Z Liu; A Gal; N Salem; A Mansour; S Blanchard; I Kobayashi; B J Keats; R Slim; C Petit
Journal:  Nat Genet       Date:  2000-09       Impact factor: 38.330

4.  The mechanosensory structure of the hair cell requires clarin-1, a protein encoded by Usher syndrome III causative gene.

Authors:  Ruishuang Geng; Sami Melki; Daniel H-C Chen; Guilian Tian; David N Furness; Tomoko Oshima-Takago; Jakob Neef; Tobias Moser; Charles Askew; Geoff Horwitz; Jeffrey R Holt; Yoshikazu Imanishi; Kumar N Alagramam
Journal:  J Neurosci       Date:  2012-07-11       Impact factor: 6.167

Review 5.  The intrinsic and extrinsic effects of N-linked glycans on glycoproteostasis.

Authors:  Daniel N Hebert; Lydia Lamriben; Evan T Powers; Jeffery W Kelly
Journal:  Nat Chem Biol       Date:  2014-10-17       Impact factor: 15.040

Review 6.  Biological and chemical approaches to diseases of proteostasis deficiency.

Authors:  Evan T Powers; Richard I Morimoto; Andrew Dillin; Jeffery W Kelly; William E Balch
Journal:  Annu Rev Biochem       Date:  2009       Impact factor: 23.643

7.  Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton.

Authors:  Guilian Tian; Yun Zhou; Dagmar Hajkova; Masaru Miyagi; Astra Dinculescu; William W Hauswirth; Krzysztof Palczewski; Ruishuang Geng; Kumar N Alagramam; Juha Isosomppi; Eeva-Marja Sankila; John G Flannery; Yoshikazu Imanishi
Journal:  J Biol Chem       Date:  2009-05-07       Impact factor: 5.157

8.  Zebrafish Models for the Mechanosensory Hair Cell Dysfunction in Usher Syndrome 3 Reveal That Clarin-1 Is an Essential Hair Bundle Protein.

Authors:  Suhasini R Gopal; Daniel H-C Chen; Shih-Wei Chou; Jingjing Zang; Stephan C F Neuhauss; Ruben Stepanyan; Brian M McDermott; Kumar N Alagramam
Journal:  J Neurosci       Date:  2015-07-15       Impact factor: 6.167

9.  Complexes of Usher proteins preassemble at the endoplasmic reticulum and are required for trafficking and ER homeostasis.

Authors:  Bernardo Blanco-Sánchez; Aurélie Clément; Javier Fierro; Philip Washbourne; Monte Westerfield
Journal:  Dis Model Mech       Date:  2014-03-13       Impact factor: 5.758

10.  A small molecule mitigates hearing loss in a mouse model of Usher syndrome III.

Authors:  Kumar N Alagramam; Suhasini R Gopal; Ruishuang Geng; Daniel H-C Chen; Ina Nemet; Richard Lee; Guilian Tian; Masaru Miyagi; Karine F Malagu; Christopher J Lock; William R K Esmieu; Andrew P Owens; Nicola A Lindsay; Krista Ouwehand; Faywell Albertus; David F Fischer; Roland W Bürli; Angus M MacLeod; William E Harte; Krzysztof Palczewski; Yoshikazu Imanishi
Journal:  Nat Chem Biol       Date:  2016-04-25       Impact factor: 15.040
  10 in total
  2 in total

Review 1.  Usher syndrome IIIA: a review of the disorder and preclinical research advances in therapeutic approaches.

Authors:  Azmi Marouf; Benjamin Johnson; Kumar N Alagramam
Journal:  Hum Genet       Date:  2022-03-23       Impact factor: 4.132

2.  Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss.

Authors:  Safoura Zardadi; Ehsan Razmara; Golareh Asgaritarghi; Ehsan Jafarinia; Fatemeh Bitarafan; Sima Rayat; Navid Almadani; Saeid Morovvati; Masoud Garshasbi
Journal:  Mol Genet Genomic Med       Date:  2020-11-18       Impact factor: 2.183
  2 in total

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