PMC Links for GEO Profiles (Select 91688730) - PMC

Select item 103990631.

Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutation

Jing Wang, Yanchun Ji, Cheng Ai, Jia-Rong Chen, Dingyi Gan, Juanjuan Zhang, Jun Q. Mo, Min-Xin Guan

J Biomed Sci. 2023; 30: 63. Published online 2023 Aug 3. doi: 10.1186/s12929-023-00951-1

PMCID:: PMC10399063

Abstract Article PDF–10M

Select item 81881982.

Hypermethylation of Hepatic Mitochondrial ND6 Provokes Systemic Insulin Resistance

Ke Cao, Weiqiang Lv, Xueqiang Wang, Shanshan Dong, Xuyun Liu, Tielin Yang, Jie Xu, Mengqi Zeng, Xuan Zou, Daina Zhao, Qingqing Ma, Mu Lin, Jiangang Long, Weijin Zang, Feng Gao, Zhihui Feng, Jiankang Liu

Adv Sci (Weinh) 2021 Jun; 8(11): 2004507. Published online 2021 May 2. doi: 10.1002/advs.202004507

PMCID:: PMC8188198

Abstract Article PDF–4.4M

Select item 81650303.

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

Abstract Article PDF–2.2M

Select item 80924664.

Circulating mitochondrial N-formyl peptides contribute to secondary nosocomial infection in patients with septic shock

Woon Yong Kwon, Gil Joon Suh, Yoon Sun Jung, Seung Min Park, Subi Oh, Sung Hee Kim, A. Rum Lee, Jeong Yeon Kim, Hayoung Kim, Kyung Ah Kim, Young Kim, Byoung Choul Kim, Taegyun Kim, Kyung Su Kim, Kiyoshi Itagaki, Carl J. Hauser

Proc Natl Acad Sci U S A. 2021 Apr 27; 118(17): e2018538118. Published online 2021 Apr 22. doi: 10.1073/pnas.2018538118

PMCID:: PMC8092466

Abstract Article PDF–1.8M

Select item 80761525.

Impact of Mitochondrial Genetic Variants in ND1, ND2, ND5, and ND6 Genes on Sperm Motility and Intracytoplasmic Sperm Injection (ICSI) Outcomes

Mohammad A. Al Smadi, Mohamad Eid Hammadeh, Erich Solomayer, Osamah Batiha, Mohammad M. Altalib, Mohammad Y. Jahmani, Mohammad A. Shboul, Bassam Nusair, Houda Amor

Reprod Sci. 2021 May; 28(5): 1540–1555. Published online 2021 Jan 21. doi: 10.1007/s43032-020-00449-3

PMCID:: PMC8076152

Abstract Article PDF–2.1M

Select item 60567206.

Assembly of mammalian oxidative phosphorylation complexes I–V and supercomplexes

Alba Signes, Erika Fernandez-Vizarra

Essays Biochem. 2018 Jul 20; 62(3): 255–270. Published online 2018 Jul 20. doi: 10.1042/EBC20170098

PMCID:: PMC6056720

Abstract Article PDF–1.5M

Select item 59532277.

Leber’s hereditary optic neuropathy (LHON) in an Apulian cohort of subjects

ANGELICA BIANCO, LUIGI BISCEGLIA, PAOLO TREROTOLI, LUCIANA RUSSO, LEONARDO D’AGRUMA, SILVANA GUERRIERO, VITTORIA PETRUZZELLA

Acta Myol. 2017 Sep; 36(3): 163–177. Published online 2017 Sep 1.

PMCID:: PMC5953227

Abstract Article PDF–156K

Select item 57657378.

Next Generation Sequencing expression profiling of mitochondrial subunits in men with Klinefelter syndrome

Michele Salemi, Laura Cimino, Marika Marino, Rossella Cannarella, Rosita A. Condorelli, Corrado Romano, Sandro La Vignera, Aldo E. Calogero

Int J Med Sci. 2018; 15(1): 31–35. Published online 2018 Jan 1. doi: 10.7150/ijms.21075

PMCID:: PMC5765737

Abstract Article PDF–332K

Select item 57005849.

Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population

Anushree Mishra, Saranya Devi, Rohit Saxena, Neerja Gupta, Madhulika Kabra, Madhumita Roy Chowdhury

Indian J Ophthalmol. 2017 Nov; 65(11): 1156–1160. doi: 10.4103/ijo.IJO_380_17

PMCID:: PMC5700584

Abstract Article PDF–723K

Select item 570057310.

Mitochondrial genetics and therapeutic overview of Leber's hereditary optic neuropathy

Agaath Hedina Manickam, Minu Jenifer Michael, Sivasamy Ramasamy

Indian J Ophthalmol. 2017 Nov; 65(11): 1087–1092. doi: 10.4103/ijo.IJO_358_17

PMCID:: PMC5700573

Abstract Article PDF–431K

Select item 402382511.

TIMMDC1/C3orf1 Functions as a Membrane-Embedded Mitochondrial Complex I Assembly Factor through Association with the MCIA Complex

Virginia Guarani, Joao Paulo, Bo Zhai, Edward L. Huttlin, Steven P. Gygi, J. Wade Harper

Mol Cell Biol. 2014 Mar; 34(5): 847–861. doi: 10.1128/MCB.01551-13

PMCID:: PMC4023825

Abstract Article PDF–5.5M

Select item 330272912.

YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation

Lukas Stiburek, Jana Cesnekova, Olga Kostkova, Daniela Fornuskova, Kamila Vinsova, Laszlo Wenchich, Josef Houstek, Jiri Zeman

Mol Biol Cell. 2012 Mar 15; 23(6): 1010–1023. doi: 10.1091/mbc.E11-08-0674

PMCID:: PMC3302729

Abstract Article PDF–1.8M

Select item 316943213.

Protein interactome reveals converging molecular pathways among autism disorders

Yasunari Sakai, Chad A. Shaw, Brian C. Dawson, Diana V. Dugas, Zaina Al-Mohtaseb, David E. Hill, Huda Y. Zoghbi

Sci Transl Med. Author manuscript; available in PMC 2011 Dec 8.

Published in final edited form as: Sci Transl Med. 2011 Jun 8; 3(86): 86ra49. doi: 10.1126/scitranslmed.3002166

PMCID:: PMC3169432

Abstract Article PDF–6.0M

Select item 284039014.

Granzyme A Cleaves a Mitochondrial Complex I Protein to Initiate Caspase-Independent Cell Death

Denis Martinvalet, Derek M. Dykxhoorn, Roger Ferrini, Judy Lieberman

Cell. Author manuscript; available in PMC 2010 Mar 17.

Published in final edited form as: Cell. 2008 May 16; 133(4): 681–692. doi: 10.1016/j.cell.2008.03.032

PMCID:: PMC2840390

Abstract Article PDF–3.3M

Select item 280000915.

Pediatric-Onset Dystonia Associated with Bilateral Striatal Necrosis and G14459A Mutation in a Korean Family: A Case Report

In-Suk Kim, Chang-Seok Ki, Ki-Jong Park

J Korean Med Sci. 2010 Jan; 25(1): 180–184. Published online 2009 Dec 26. doi: 10.3346/jkms.2010.25.1.180

PMCID:: PMC2800009

Abstract Article PDF–211K

Select item 278500116.

Leber’s hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation

Fuxin Zhao, Minqiang Guan, Xiangtian Zhou, Meixia Yuan, Ming Liang, Qi Liu, Yan Liu, Yongmei Zhang, Li Yang, Yi Tong, Qi-Ping Wei, Yan-Hong Sun, Jia Qu, Min-Xin Guan

Biochem Biophys Res Commun. Author manuscript; available in PMC 2010 Nov 20.

Published in final edited form as: Biochem Biophys Res Commun. 2009 Nov 20; 389(3): 466–472. Published online 2009 Sep 2. doi: 10.1016/j.bbrc.2009.08.168