Literature DB >> 27718101

Erratum to: Mitochondrial CHCHD-Containing Proteins: Physiologic Functions and Link with Neurodegenerative Diseases.

Zhi-Dong Zhou1,2, Wuan-Ting Saw3, Eng-King Tan4,5,6.   

Abstract

Entities:  

Year:  2017        PMID： 27718101     DOI： 10.1007/s12035-016-0160-4

Source DB:  PubMed          Journal:  Mol Neurobiol        ISSN： 0893-7648            Impact factor:   5.590


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  12 in total

1.  High prevalence of CHCHD10 mutation in patients with frontotemporal dementia from China.

Authors:  Bin Jiao; Tingting Xiao; Lihua Hou; Xiaohua Gu; Yafang Zhou; Lin Zhou; Beisha Tang; Jun Xu; Lu Shen
Journal:  Brain       Date:  2015-12-30       Impact factor: 13.501

2.  Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients.

Authors:  Annabelle Chaussenot; Isabelle Le Ber; Samira Ait-El-Mkadem; Agnès Camuzat; Anne de Septenville; Sylvie Bannwarth; Emmanuelle C Genin; Valérie Serre; Gaëlle Augé; Alexis Brice; Jean Pouget; Véronique Paquis-Flucklinger
Journal:  Neurobiol Aging       Date:  2014-07-24       Impact factor: 4.673

3.  CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients.

Authors:  Adriano Chiò; Gabriele Mora; Mario Sabatelli; Claudia Caponnetto; Bryan J Traynor; Janel O Johnson; Mike A Nalls; Andrea Calvo; Cristina Moglia; Giuseppe Borghero; Maria Rosaria Monsurrò; Vincenzo La Bella; Paolo Volanti; Isabella Simone; Fabrizio Salvi; Francesco O Logullo; Riva Nilo; Stefania Battistini; Jessica Mandrioli; Raffaella Tanel; Maria Rita Murru; Paola Mandich; Marcella Zollino; Francesca L Conforti; Maura Brunetti; Marco Barberis; Gabriella Restagno; Silvana Penco; Christian Lunetta
Journal:  Neurobiol Aging       Date:  2015-01-28       Impact factor: 4.673

4.  CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.

Authors:  Dario Ronchi; Giulietta Riboldi; Roberto Del Bo; Nicola Ticozzi; Marina Scarlato; Daniela Galimberti; Stefania Corti; Vincenzo Silani; Nereo Bresolin; Giacomo Pietro Comi
Journal:  Brain       Date:  2015-01-08       Impact factor: 13.501

5.  Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease.

Authors:  Kathrin Müller; Peter M Andersen; Annemarie Hübers; Nicolai Marroquin; Alexander E Volk; Karin M Danzer; Thomas Meitinger; Albert C Ludolph; Tim M Strom; Jochen H Weishaupt
Journal:  Brain       Date:  2014-08-11       Impact factor: 13.501

6.  Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.

Authors:  Janel O Johnson; Shannon M Glynn; J Raphael Gibbs; Mike A Nalls; Mario Sabatelli; Gabriella Restagno; Vivian E Drory; Adriano Chiò; Ekaterina Rogaeva; Bryan J Traynor
Journal:  Brain       Date:  2014-09-26       Impact factor: 13.501

7.  Late onset spinal motor neuronopathy is caused by mutation in CHCHD10.

Authors:  Sini Penttilä; Manu Jokela; Heidi Bouquin; Anna Maija Saukkonen; Jari Toivanen; Bjarne Udd
Journal:  Ann Neurol       Date:  2014-12-12       Impact factor: 10.422

8.  Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy.

Authors:  Senda Ajroud-Driss; Faisal Fecto; Kaouther Ajroud; Irfan Lalani; Sarah E Calvo; Vamsi K Mootha; Han-Xiang Deng; Nailah Siddique; Albert J Tahmoush; Terry D Heiman-Patterson; Teepu Siddique
Journal:  Neurogenetics       Date:  2014-09-06       Impact factor: 2.660

9.  Mutation analysis of CHCHD10 in different neurodegenerative diseases.

Authors:  Ming Zhang; Zhengrui Xi; Lorne Zinman; Amalia C Bruni; Raffaele G Maletta; Sabrina A M Curcio; Innocenzo Rainero; Elisa Rubino; Lorenzo Pinessi; Benedetta Nacmias; Sandro Sorbi; Daniela Galimberti; Anthony E Lang; Susan Fox; Ezequiel I Surace; Mahdi Ghani; Jing Guo; Christine Sato; Danielle Moreno; Yan Liang; Julia Keith; Bryan J Traynor; Peter St George-Hyslop; Ekaterina Rogaeva
Journal:  Brain       Date:  2015-03-31       Impact factor: 13.501

10.  Cloning and functional analysis of FLJ20420: a novel transcription factor for the BAG-1 promoter.

Authors:  Hongyu Liu; Ying Li; Yongwen Li; Baoxin Liu; Heng Wu; Jing Wang; Yuli Wang; Min Wang; Shou-Ching Tang; Qinghua Zhou; Jun Chen
Journal:  PLoS One       Date:  2012-05-02       Impact factor: 3.240
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