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Items: 1 to 20 of 32

1.
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
2.
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
3.
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
4.
CFTR interactome mapping using the mammalian membrane two‐hybrid high‐throughput screening system
Sang Hyun Lim, Jamie Snider, Liron Birimberg‐Schwartz, Wan Ip, Joana C Serralha, Hugo M Botelho, Miquéias Lopes‐Pacheco, Madalena C Pinto, Mohamed Taha Moutaoufik, Mara Zilocchi, Onofrio Laselva, Mohsen Esmaeili, Max Kotlyar, Anna Lyakisheva, Priscilla Tang, Lucía López Vázquez, Indira Akula, Farzaneh Aboualizadeh, Victoria Wong, Ingrid Grozavu, Teuta Opacak‐Bernardi, Zhong Yao, Meg Mendoza, Mohan Babu, Igor Jurisica, Tanja Gonska, Christine E Bear, Margarida D Amaral, Igor Stagljar
Mol Syst Biol. 2022 Feb; 18(2): e10629. Published online 2022 Feb 14. doi: 10.15252/msb.202110629
PMCID:
PMC8842165
AbstractArticlePDF–3.0M
5.
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
6.
Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome
Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2022 May 27.
Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011
PMCID:
PMC8165030
AbstractArticlePDF–2.2M
7.
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
8.
Systematic mapping of genetic interactions for de novo fatty acid synthesis identifies C12orf49 as a regulator of lipid metabolism
Michael Aregger, Keith A. Lawson, Maximillian Billmann, Michael Costanzo, Amy H. Y. Tong, Katherine Chan, Mahfuzur Rahman, Kevin R. Brown, Catherine Ross, Matej Usaj, Lucy Nedyalkova, Olga Sizova, Andrea Habsid, Judy Pawling, Zhen-Yuan Lin, Hala Abdouni, Cassandra J. Wong, Alexander Weiss, Patricia Mero, James W. Dennis, Anne-Claude Gingras, Chad L. Myers, Brenda J. Andrews, Charles Boone, Jason Moffat
Nat Metab. Author manuscript; available in PMC 2020 Dec 1.
Published in final edited form as: Nat Metab. 2020 Jun; 2(6): 499–513. Published online 2020 Jun 1. doi: 10.1038/s42255-020-0211-z
PMCID:
PMC7566881
AbstractArticlePDF–4.8M
9.
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
10.
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
11.
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
12.
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
13.
CHCHD2 accumulates in distressed mitochondria and facilitates oligomerization of CHCHD10
Xiaoping Huang, Beverly P Wu, Diana Nguyen, Yi-Ting Liu, Melika Marani, Jürgen Hench, Paule Bénit, Vera Kozjak-Pavlovic, Pierre Rustin, Stephan Frank, Derek P Narendra
Hum Mol Genet. 2018 Nov 15; 27(22): 3881–3900. Published online 2018 Jul 31. doi: 10.1093/hmg/ddy270
Correction in:
Hum Mol Genet. 2019 Jan 15; 28(2): 349.
PMCID:
PMC6216204
AbstractArticlePDF–68M
14.
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
15.
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
16.
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
17.
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
18.
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
19.
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
20.
Architecture of the human interactome defines protein communities and disease networks
Edward L. Huttlin, Raphael J. Bruckner, Joao A. Paulo, Joe R. Cannon, Lily Ting, Kurt Baltier, Greg Colby, Fana Gebreab, Melanie P. Gygi, Hannah Parzen, John Szpyt, Stanley Tam, Gabriela Zarraga, Laura Pontano-Vaites, Sharan Swarup, Anne E. White, Devin K. Schweppe, Ramin Rad, Brian K. Erickson, Robert A. Obar, K.G. Guruharsha, Kejie Li, Spyros Artavanis-Tsakonas, Steven P. Gygi, J. Wade Harper
Nature. Author manuscript; available in PMC 2017 Nov 17.
Published in final edited form as: Nature. 2017 May 25; 545(7655): 505–509. Published online 2017 May 17. doi: 10.1038/nature22366
PMCID:
PMC5531611
AbstractArticlePDF–2.7M

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