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Items: 1 to 20 of 33

1.
High CpG island methylator phenotype is associated with lymph node metastasis and prognosis in gastric cancer
Hua‐Yun Chen, Bao‐He Zhu, Chang‐Hua Zhang, Dong‐Jie Yang, Jian‐Jun Peng, Jian‐Hui Chen, Fa‐Keng Liu, Yu‐Long He
Cancer Sci. 2012 Jan; 103(1): 73–79. Published online 2011 Nov 24. doi: 10.1111/j.1349-7006.2011.02129.x
PMCID:
PMC11164149
AbstractArticlePDF–305K
2.
Multi-OMICS study of a CHCHD10 variant causing ALS demonstrates metabolic rewiring and activation of endoplasmic reticulum and mitochondrial unfolded protein responses
Isabella R Straub, Woranontee Weraarpachai, Eric A Shoubridge
Hum Mol Genet. 2021 Apr 15; 30(8): 687–705. Published online 2021 Mar 22. doi: 10.1093/hmg/ddab078
PMCID:
PMC8127406
AbstractArticlePDF–1.9M
3.
CHCHD10 variants in Amyotrophic Lateral Sclerosis: where is the evidence?
Project MinE ALS Sequencing Consortium
Ann Neurol. Author manuscript; available in PMC 2019 Jul 1.
Published in final edited form as: Ann Neurol. 2018 Jul; 84(1): 110–116. doi: 10.1002/ana.25273
PMCID:
PMC6553489
AbstractArticlePDF–485K
4.
Identification of CHCHD10 variants in Chinese patients with Parkinson’s disease
Xiaoxia Zhou, Zhenhua Liu, Jifeng Guo, Qiying Sun, Qian Xu, Xinxiang Yan, Beisha Tang, Lifang Lei
Parkinsonism Relat Disord. Author manuscript; available in PMC 2018 Jun 11.
Published in final edited form as: Parkinsonism Relat Disord. 2018 Feb; 47: 96–97. Published online 2017 Dec 8. doi: 10.1016/j.parkreldis.2017.12.002
PMCID:
PMC5995111
ArticlePDF–290K
5.
A novel CHCHD10 mutation implicates a Mia40‐dependent mitochondrial import deficit in ALS
Carina Lehmer, Martin H Schludi, Linnea Ransom, Johanna Greiling, Michaela Junghänel, Nicole Exner, Henrick Riemenschneider, Julie van der Zee, Christine Van Broeckhoven, Patrick Weydt, Michael T Heneka, Dieter Edbauer
EMBO Mol Med. 2018 Jun; 10(6): e8558. Published online 2018 May 22. doi: 10.15252/emmm.201708558
PMCID:
PMC5991575
AbstractArticlePDF–2.2M
6.
CHCHD10 Pro34Ser is not a highly penetrant pathogenic variant for amyotrophic lateral sclerosis and frontotemporal dementia
Samir Abdelkarim, Sarah Morgan, Vincent Plagnol, Ching-Hua Lu, Gary Adamson, Robin Howard, Andrea Malaspina, Richard Orrell, Nikhil Sharma, Katie Sidle, Jan Clarke, Nick C. Fox, Martin N. Rossor, Jason D. Warren, Camilla N. Clark, Jonathan D. Rohrer, Elizabeth M. C. Fisher, Simon Mead, Alan Pittman, Pietro Fratta
Brain. 2016 Feb; 139(2): e9. Published online 2015 Sep 11. doi: 10.1093/brain/awv223
PMCID:
PMC5963427
ArticlePDF–161K
7.
Mutation in the Novel Nuclear-Encoded Mitochondrial Protein CHCHD10 in a Family with Autosomal Dominant Mitochondrial Myopathy
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
Neurogenetics. Author manuscript; available in PMC 2016 Mar 18.
Published in final edited form as: Neurogenetics. 2015 Jan; 16(1): 1–9. Published online 2014 Sep 6. doi: 10.1007/s10048-014-0421-1
PMCID:
PMC4796476
AbstractArticlePDF–484K
8.
CHCH10 mutations in an Italian cohort of familial and sporadic ALS patients
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, ITALSGEN consortium, Maura Brunetti, Marco Barberis, Gabriella Restagno, Silvana Penco, Christian Lunetta
Neurobiol Aging. Author manuscript; available in PMC 2016 Apr 1.
Published in final edited form as: Neurobiol Aging. 2015 Apr; 36(4): 1767.e3–1767.e6. Published online 2015 Jan 28. doi: 10.1016/j.neurobiolaging.2015.01.017
PMCID:
PMC4380794
AbstractArticlePDF–150K
9.
Disruption of Mitophagy Flux through the PARL-PINK1 Pathway by CHCHD10 Mutations or CHCHD10 Depletion
Tian Liu, Liam Wetzel, Zexi Zhu, Pavan Kumaraguru, Viraj Gorthi, Yan Yan, Mohammed Zaheen Bukhari, Aizara Ermekbaeva, Hanna Jeon, Teresa R. Kee, Jung-A Alexa Woo, David E. Kang
Cells. 2023 Dec; 12(24): 2781. Published online 2023 Dec 7. doi: 10.3390/cells12242781
PMCID:
PMC10741529
AbstractArticlePDF–3.5M
10.
Modulation of synaptic plasticity, motor unit physiology, and TDP-43 pathology by CHCHD10
Tian Liu, Jung-A. A. Woo, Mohammed Zaheen Bukhari, Xinming Wang, Yan Yan, Sara Cazzaro Buosi, Aizara Ermekbaeva, Apoorva Sista, Peter Kotsiviras, Patrick LePochat, Ann Chacko, Xingyu Zhao, David E. Kang
Acta Neuropathol Commun. 2022; 10: 95. Published online 2022 Jul 4. doi: 10.1186/s40478-022-01386-9
PMCID:
PMC9254494
AbstractArticlePDF–7.5M
11.
CHCHD2 and CHCHD10 regulate mitochondrial dynamics and integrated stress response
Yu Ruan, Jiaqiao Hu, Yaping Che, Yanyan Liu, Zhenhuan Luo, Jin Cheng, Qi Han, He He, Qinghua Zhou
Cell Death Dis. 2022 Feb; 13(2): 156. Published online 2022 Feb 16. doi: 10.1038/s41419-022-04602-5
PMCID:
PMC8850591
AbstractArticlePDF–11M
12.
CHCHD10 is involved in the development of Parkinson’s disease caused by CHCHD2 loss-of-function mutation p.T61I
Chengyuan Mao, Herui Wang, Haiyang Luo, Shuyu Zhang, Huisha Xu, Shuo Zhang, Jared Rosenblum, Zhilei Wang, Qi Zhang, Mibo Tang, Matthew J. Shepard, Xiang Wang, Yaohe Wang, Zhengping Zhuang, Changhe Shi, Yuming Xu
Neurobiol Aging. Author manuscript; available in PMC 2021 Jul 29.
Published in final edited form as: Neurobiol Aging. 2019 Mar; 75: 38–41. Published online 2018 Oct 23. doi: 10.1016/j.neurobiolaging.2018.10.020
PMCID:
PMC8320701
AbstractArticlePDF–917K
13.
PD-linked CHCHD2 mutations impair CHCHD10 and MICOS complex leading to mitochondria dysfunction
Wei Zhou, Dongrui Ma, Alfred Xuyang Sun, Hoang-Dai Tran, Dong-liang Ma, Brijesh K Singh, Jin Zhou, Jinyan Zhang, Danlei Wang, Yi Zhao, Paul M Yen, Eyleen Goh, Eng-King Tan
Hum Mol Genet. 2019 Apr 1; 28(7): 1100–1116. Published online 2018 Nov 29. doi: 10.1093/hmg/ddy413
PMCID:
PMC6423417
AbstractArticlePDF–58M
14.
The cellular stress proteins CHCHD10 and MNRR1 (CHCHD2): Partners in mitochondrial and nuclear function and dysfunction
Neeraja Purandare, Mallika Somayajulu, Maik Hüttemann, Lawrence I. Grossman, Siddhesh Aras
J Biol Chem. 2018 Apr 27; 293(17): 6517–6529. Published online 2018 Mar 14. doi: 10.1074/jbc.RA117.001073
PMCID:
PMC5925800
AbstractArticlePDF–2.1M
15.
In vitro and in vivo studies of the ALS-FTLD protein CHCHD10 reveal novel mitochondrial topology and protein interactions
S R Burstein, F Valsecchi, H Kawamata, M Bourens, R Zeng, A Zuberi, T A Milner, S M Cloonan, C Lutz, A Barrientos, G Manfredi
Hum Mol Genet. 2018 Jan 1; 27(1): 160–177. Published online 2017 Nov 3. doi: 10.1093/hmg/ddx397
PMCID:
PMC5886281
AbstractArticlePDF–1.9M
16.
Loss of CHCHD10–CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALS
Isabella R Straub, Alexandre Janer, Woranontee Weraarpachai, Lorne Zinman, Janice Robertson, Ekaterina Rogaeva, Eric A Shoubridge
Hum Mol Genet. 2018 Jan 1; 27(1): 178–189. Published online 2017 Nov 7. doi: 10.1093/hmg/ddx393
PMCID:
PMC5886208
AbstractArticlePDF–1.1M
17.
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement
Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, Emmanuelle C. Genin, Sandra Lacas-Gervais, Konstantina Fragaki, Laetitia Berg-Alonso, Yusuke Kageyama, Valérie Serre, David G. Moore, Annie Verschueren, Cécile Rouzier, Isabelle Le Ber, Gaëlle Augé, Charlotte Cochaud, Françoise Lespinasse, Karine N’Guyen, Anne de Septenville, Alexis Brice, Patrick Yu-Wai-Man, Hiromi Sesaki, Jean Pouget, Véronique Paquis-Flucklinger
Brain. 2014 Aug; 137(8): 2329–2345. Published online 2014 Jun 13. doi: 10.1093/brain/awu138
PMCID:
PMC4107737
AbstractArticlePDF–1.8M
18.
Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseases
Emmanuelle C. Genin, Sylvie Bannwarth, Françoise Lespinasse, Bernardo Ortega-Vila, Konstantina Fragaki, Kie Itoh, Elodie Villa, Sandra Lacas-Gervais, Manu Jokela, Mari Auranen, Emil Ylikallio, Alessandra Mauri-Crouzet, Henna Tyynismaa, Anna Vihola, Gaelle Augé, Charlotte Cochaud, Hiromi Sesaki, Jean-Ehrland Ricci, Bjarne Udd, Cristofol Vives-Bauza, Véronique Paquis-Flucklinger
Neurobiol Dis. Author manuscript; available in PMC 2020 Feb 12.
Published in final edited form as: Neurobiol Dis. 2018 Nov; 119: 159–171. Published online 2018 Aug 6. doi: 10.1016/j.nbd.2018.07.027
PMCID:
PMC7015038
AbstractArticlePDF–2.1M
19.
CHCHD10-regulated OPA1-mitofilin complex mediates TDP-43-induced mitochondrial phenotypes associated with Frontotemporal dementia
Tian Liu, Jung-A A. Woo, Mohammed Zaheen Bukhari, Patrick LePochat, Ann Chacko, Maj-Linda B. Selenica, Yan Yan, Peter Kotsiviras, Sara Cazzaro Buosi, Xingyu Zhao, David E. Kang
FASEB J. Author manuscript; available in PMC 2021 Jun 1.
Published in final edited form as: FASEB J. 2020 Jun; 34(6): 8493–8509. Published online 2020 May 5. doi: 10.1096/fj.201903133RR
PMCID:
PMC7482311
AbstractArticlePDF–1.3M
20.
CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis
Emmanuelle C Genin, Morgane Plutino, Sylvie Bannwarth, Elodie Villa, Eugenia Cisneros‐Barroso, Madhuparna Roy, Bernardo Ortega‐Vila, Konstantina Fragaki, Françoise Lespinasse, Estefania Pinero‐Martos, Gaëlle Augé, David Moore, Florence Burté, Sandra Lacas‐Gervais, Yusuke Kageyama, Kie Itoh, Patrick Yu‐Wai‐Man, Hiromi Sesaki, Jean‐Ehrland Ricci, Cristofol Vives‐Bauza, Véronique Paquis‐Flucklinger
EMBO Mol Med. 2016 Jan; 8(1): 58–72. Published online 2015 Dec 14. doi: 10.15252/emmm.201505496
PMCID:
PMC4718158
AbstractArticlePDF–2.2M

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