PMC Links for Gene (Select 4538) - PMC

Links from Gene

Items: 1 to 20 of 39

<< First< Prev

Page of 2

Next >Last >>

Select item 102962571.

Mitochondrial Diabetes Is Associated with the ND4 G11696A Mutation

Yu Ding, Shunrong Zhang, Qinxian Guo, Jianhang Leng

Biomolecules. 2023 Jun; 13(6): 907. Published online 2023 May 30. doi: 10.3390/biom13060907

PMCID:: PMC10296257

Abstract Article PDF–3.2M

Select item 101938092.

A small protein coded within the mitochondrial canonical gene nd4 regulates mitochondrial bioenergetics

Laura Kienzle, Stefano Bettinazzi, Thierry Choquette, Marie Brunet, Hajar Hosseini Khorami, Jean-François Jacques, Mathilde Moreau, Xavier Roucou, Christian R. Landry, Annie Angers, Sophie Breton

BMC Biol. 2023; 21: 111. Published online 2023 May 18. doi: 10.1186/s12915-023-01609-y

PMCID:: PMC10193809

Abstract Article PDF–2.0M

Select item 84171583.

Mitochondrial nicotinamide adenine dinucleotide hydride dehydrogenase (NADH) subunit 4 (MTND4) polymorphisms and their association with male infertility

Fatina W. Dahadhah, Mayyas Saleh Jaweesh, Mazhar Salim Al Zoubi, Manal Issam Abu Alarjah, Mohamad Eid Hammadeh, Houda Amor

J Assist Reprod Genet. 2021 Aug; 38(8): 2021–2029. Published online 2021 Apr 24. doi: 10.1007/s10815-021-02199-w

PMCID:: PMC8417158

Abstract Article PDF–345K

Select item 62961454.

Juvenile open-angle Glaucoma associated with Leber’s hereditary optic neuropathy: a case report and literature review

Yun-Hsuan Lin, Nan-Kai Wang, Ling Yeung, Chi-Chun Lai, Lan-Hsin Chuang

BMC Ophthalmol. 2018; 18: 323. Published online 2018 Dec 17. doi: 10.1186/s12886-018-0980-2

PMCID:: PMC6296145

Abstract Article PDF–5.5M

Select item 50484825.

Male-specific association between MT-ND4 11719 A/G polymorphism and ulcerative colitis: a mitochondria-wide genetic association study

Theresa Dankowski, Torsten Schröder, Steffen Möller, Xinhua Yu, David Ellinghaus, Florian Bär, Klaus Fellermann, Hendrik Lehnert, Stefan Schreiber, Andre Franke, Christian Sina, Saleh M. Ibrahim, Inke R. König

BMC Gastroenterol. 2016; 16: 118. Published online 2016 Oct 3. doi: 10.1186/s12876-016-0509-1

PMCID:: PMC5048482

Abstract Article PDF–462K

Select item 34317966.

Induction of Rapid and Highly Efficient Expression of the Human ND4 Complex I Subunit in the Mouse Visual System by Self-complementary Adeno-Associated Virus

Rajeshwari D. Koilkonda, Tsung-Han Chou, Vittorio Porciatti, William W. Hauswirth, John Guy

Arch Ophthalmol. Author manuscript; available in PMC 2012 Aug 31.

Published in final edited form as: Arch Ophthalmol. 2010 Jul; 128(7): 876–883. doi: 10.1001/archophthalmol.2010.135

PMCID:: PMC3431796

Abstract Article PDF–2.1M

Select item 33566437.

Gene delivery to mitochondria by targeting modified adenoassociated virus suppresses Leber’s hereditary optic neuropathy in a mouse model

Hong Yu, Rajeshwari D. Koilkonda, Tsung-Han Chou, Vittorio Porciatti, Sacide S. Ozdemir, Vince Chiodo, Sanford L. Boye, Shannon E. Boye, William W. Hauswirth, Alfred S. Lewin, John Guy

Proc Natl Acad Sci U S A. 2012 May 15; 109(20): E1238–E1247. Published online 2012 Apr 20. doi: 10.1073/pnas.1119577109

PMCID:: PMC3356643

Abstract Article PDF–2.7M

Select item 32200558.

Leber Hereditary Optic Neuropathy Gene Therapy Clinical Trial Recruitment: Year 1

Byron L. Lam, William J. Feuer, Fawzi Abukhalil, Vittorio Porciatti, William W. Hauswirth, John Guy

Arch Ophthalmol. Author manuscript; available in PMC 2011 Nov 18.

Published in final edited form as: Arch Ophthalmol. 2010 Sep; 128(9): 1129–1135. doi: 10.1001/archophthalmol.2010.201

PMCID:: PMC3220055

Abstract Article PDF–940K

Select item 29071619.

Extremely Low Penetrance of Leber’s Hereditary Optic Neuropathy in 8 Han Chinese Families Carrying the ND4 G11778A Mutation

Jia Qu, Xiangtian Zhou, Juanjuan Zhang, Fuxin Zhao, Yan-Hong Sun, Yi Tong, Qi-Ping Wei, Wansi Cai, Li Yang, Constance E. West, Min-Xin Guan

Ophthalmology. Author manuscript; available in PMC 2010 Jul 20.

Published in final edited form as: Ophthalmology. 2009 Mar; 116(3): 558–564.e3. Published online 2009 Jan 22. doi: 10.1016/j.ophtha.2008.10.022

PMCID:: PMC2907161

Abstract Article PDF–452K

Select item 290664110.

Very high penetrance and occurrence of Leber’s hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation

Xiangtian Zhou, Hongxing Zhang, Fuxin Zhao, Yanchun Ji, Yi Tong, Juanjuan Zhang, Yu Zhang, Li Yang, Yaping Qian, Fan Lu, Jia Qu, Min-Xin Guan

Mol Genet Metab. Author manuscript; available in PMC 2011 Aug 1.

Published in final edited form as: Mol Genet Metab. 2010 Aug; 100(4): 379–384. Published online 2010 Apr 29. doi: 10.1016/j.ymgme.2010.04.013

PMCID:: PMC2906641

Abstract Article PDF–174K

Select item 269693611.

The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family

Zhisu Liao, Jianyue Zhao, Yi Zhu, Li Yang, Aifen Yang, Dongmei Sun, Zhongnong Zhao, Xinjian Wang, Zhihua Tao, Xiaowen Tang, Jindan Wang, Minqiang Guan, Jiafu Chen, Zhiyuan Li, Jianxin Lu, Min-Xin Guan

Biochem Biophys Res Commun. Author manuscript; available in PMC 2009 Jun 16.

Published in final edited form as: Biochem Biophys Res Commun. 2007 Oct 26; 362(3): 670–676. Published online 2007 Aug 15. doi: 10.1016/j.bbrc.2007.08.034

PMCID:: PMC2696936

Abstract Article PDF–634K

Select item 255643312.

Optimized Allotopic Expression of the Human Mitochondrial ND4 Prevents Blindness in a Rat Model of Mitochondrial Dysfunction

Sami Ellouze, Sébastien Augustin, Aicha Bouaita, Crystel Bonnet, Manuel Simonutti, Valérie Forster, Serge Picaud, Jose-Alain Sahel, Marisol Corral-Debrinski

Am J Hum Genet. 2008 Sep 12; 83(3): 373–387. Published online 2008 Sep 5. doi: 10.1016/j.ajhg.2008.08.013

PMCID:: PMC2556433

Abstract Article PDF–1.2M

Select item 201472413.

Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family

Jia Qu, Ronghua Li, Xiangtian Zhou, Yi Tong, Li Yang, Jie Chen, Fuxing Zhao, Chunjie Lu, Yaping Qian, Fan Lu, Min-Xin Guan

Mitochondrion. Author manuscript; available in PMC 2008 Feb 1.

Published in final edited form as: Mitochondrion. 2007; 7(1-2): 140–146. Published online 2006 Dec 8. doi: 10.1016/j.mito.2006.11.015

PMCID:: PMC2014724

Abstract Article PDF–324K

Select item 41356914.

Lack of assembly of mitochondrial DNA-encoded subunits of respiratory NADH dehydrogenase and loss of enzyme activity in a human cell mutant lacking the mitochondrial ND4 gene product.

G Hofhaus, G Attardi

EMBO J. 1993 Aug; 12(8): 3043–3048. doi: 10.1002/j.1460-2075.1993.tb05973.x

Correction in:: EMBO J. 1994 Dec 1; 13(23): 5794.

PMCID:: PMC413569

Summary Page Browse PDF–1.2M

Select item 968068815.

Diagnostic value of circulating cell-free mtDNA in patients with suspected thyroid cancer: ND4/ND1 ratio as a new potential plasma marker

Zhiying Jiang, Tyler Bahr, Chen Zhou, Tao Jin, Hao Chen, Shujie Song, Yuji Ikeno, Hengli Tian, Yidong Bai

Mitochondrion. Author manuscript; available in PMC 2022 Nov 22.

Published in final edited form as: Mitochondrion. 2020 Nov; 55: 145–153. Published online 2020 Oct 7. doi: 10.1016/j.mito.2020.09.007

PMCID:: PMC9680688

Abstract Article PDF–2.0M

Select item 809260916.

Optic atrophy–associated TMEM126A is an assembly factor for the ND4-module of mitochondrial complex I

Luke E. Formosa, Boris Reljic, Alice J. Sharpe, Daniella H. Hock, Linden Muellner-Wong, David A. Stroud, Michael T. Ryan

Proc Natl Acad Sci U S A. 2021 Apr 27; 118(17): e2019665118. Published online 2021 Apr 20. doi: 10.1073/pnas.2019665118

PMCID:: PMC8092609

Abstract Article PDF–1.1M

Select item 750491817.

Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy

Yanchun Ji, Juanjuan Zhang, Yuanyuan Lu, Qiuzi Yi, Mengquan Chen, Shipeng Xie, Xiaoting Mao, Yun Xiao, Feilong Meng, Minglian Zhang, Rulai Yang, Min-Xin Guan

J Biol Chem. 2020 Sep 18; 295(38): 13224–13238. Published online 2020 Jul 28. doi: 10.1074/jbc.RA120.014603

PMCID:: PMC7504918

Abstract Article PDF–5.3M

Select item 191469218.

Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.

D. D. De Vries, L. N. Went, G. W. Bruyn, H. R. Scholte, R. M. Hofstra, P. A. Bolhuis, B. A. van Oost

Am J Hum Genet. 1996 Apr; 58(4): 703–711.

PMCID:: PMC1914692

Summary Page Browse PDF–1.5M

Select item 595322719.

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 570058420.

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

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 39

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity