Literature DB >> 26067114

CHCHD2 and Parkinson's disease.

Jia Nee Foo1, Jianjun Liu1, Eng-King Tan2.   

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Year:  2015        PMID： 26067114     DOI： 10.1016/S1474-4422(15)00098-8

Source DB:  PubMed          Journal:  Lancet Neurol        ISSN： 1474-4422            Impact factor:   44.182


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  8 in total

Review 1.  Mitochondrial CHCHD-Containing Proteins: Physiologic Functions and Link with Neurodegenerative Diseases.

Authors:  Zhi-Dong Zhou; Wuan-Ting Saw; Eng-King Tan
Journal:  Mol Neurobiol       Date:  2016-09-08       Impact factor: 5.590

Review 2.  Genetic predispositions of Parkinson's disease revealed in patient-derived brain cells.

Authors:  Jenne Tran; Helena Anastacio; Cedric Bardy
Journal:  NPJ Parkinsons Dis       Date:  2020-04-24

Review 3.  Mitochondrial CHCHD2: Disease-Associated Mutations, Physiological Functions, and Current Animal Models.

Authors:  Teresa R Kee; Pamela Espinoza Gonzalez; Jessica L Wehinger; Mohammed Zaheen Bukhari; Aizara Ermekbaeva; Apoorva Sista; Peter Kotsiviras; Tian Liu; David E Kang; Jung-A A Woo
Journal:  Front Aging Neurosci       Date:  2021-04-22       Impact factor: 5.750

Review 4.  New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

Authors:  Andreas Puschmann
Journal:  Curr Neurol Neurosci Rep       Date:  2017-09       Impact factor: 5.081

Review 5.  Genetic predispositions of Parkinson's disease revealed in patient-derived brain cells.

Authors:  Jenne Tran; Helena Anastacio; Cedric Bardy
Journal:  NPJ Parkinsons Dis       Date:  2020-04-24

Review 6.  CHCHD2 and CHCHD10: Future therapeutic targets in cognitive disorder and motor neuron disorder.

Authors:  Tianlin Jiang; Yanli Wang; Xiaohong Wang; Jun Xu
Journal:  Front Neurosci       Date:  2022-08-18       Impact factor: 5.152

Review 7.  Neurodegeneration-associated mitochondrial proteins, CHCHD2 and CHCHD10-what distinguishes the two?

Authors:  Aya Ikeda; Yuzuru Imai; Nobutaka Hattori
Journal:  Front Cell Dev Biol       Date:  2022-09-09

8.  Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction.

Authors:  Richard G Lee; Maryam Sedghi; Mehri Salari; Anne-Marie J Shearwood; Maike Stentenbach; Ariana Kariminejad; Hayley Goullee; Oliver Rackham; Nigel G Laing; Homa Tajsharghi; Aleksandra Filipovska
Journal:  Neurol Genet       Date:  2018-10-05
  8 in total

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