PubMed for id: 4537

Year	Number of Results
1981	1
1985	1
1999	1
2001	1
2003	2
2004	4
2005	5
2006	3
2007	9
2008	8
2009	5
2010	1
2011	1
2012	2
2013	2
2014	3
2015	3
2016	3
2017	3
2018	4
2020	1
2021	4
2024	0

1

Metabolic Signature of MELAS/Leigh Overlap Syndrome in Patient-specific Induced Pluripotent Stem Cells Model.

Hattori T, Hamazaki T, Kudo S, Shintaku H. Hattori T, et al. Osaka City Med J. 2016 Dec;62(2):69-76. Osaka City Med J. 2016. PMID: 30721581

2

Mitochondrial NADH Dehydrogenase Subunit 3 (MTND3) Polymorphisms are Associated with Gastric Cancer Susceptibility.

Jin EH, Sung JK, Lee SI, Hong JH. Jin EH, et al. Int J Med Sci. 2018 Aug 10;15(12):1329-1333. doi: 10.7150/ijms.26881. eCollection 2018. Int J Med Sci. 2018. PMID: 30275759 Free PMC article.

3

Mitochondrial ND3 G10398A mutation: a biomarker for breast cancer.

Yu Y, Lv F, Lin H, Qian G, Jiang YS, Pang LX, Wang YP, Wang XF, Kang YM, Li CB, Liu Q, Xu JZ, You W. Yu Y, et al. Genet Mol Res. 2015 Dec 21;14(4):17426-31. doi: 10.4238/2015.December.21.12. Genet Mol Res. 2015. PMID: 26782384 Free article.

4

Mitochondrial NADH Dehydrogenase Subunit 3 Polymorphism Associated with an Earlier Age at Onset in Male Machado-Joseph disease Patients.

Chen S, Gan SR, Cai PP, Ni W, Zhou Q, Dong Y, Wang N, Wu ZY. Chen S, et al. CNS Neurosci Ther. 2016 Jan;22(1):38-42. doi: 10.1111/cns.12443. Epub 2015 Sep 4. CNS Neurosci Ther. 2016. PMID: 26336829 Free PMC article.

5

Rapid identification of a novel complex I MT-ND3 m.10134C>A mutation in a Leigh syndrome patient.

Miller DK, Menezes MJ, Simons C, Riley LG, Cooper ST, Grimmond SM, Thorburn DR, Christodoulou J, Taft RJ. Miller DK, et al. PLoS One. 2014 Aug 12;9(8):e104879. doi: 10.1371/journal.pone.0104879. eCollection 2014. PLoS One. 2014. PMID: 25118196 Free PMC article.

6

Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy.

Li YJ, Minear MA, Qin X, Rimmler J, Hauser MA, Allingham RR, Igo RP, Lass JH, Iyengar SK, Klintworth GK, Afshari NA, Gregory SG; FECD Genetics Consortium. Li YJ, et al. Invest Ophthalmol Vis Sci. 2014 Jun 10;55(7):4577-84. doi: 10.1167/iovs.13-13517. Invest Ophthalmol Vis Sci. 2014. PMID: 24917144 Free PMC article.

7

Highly expressed MT-ND3 positively associated with histological severity of hepatic steatosis.

Wang HN, Chen HD, Chen KY, Xiao JF, He K, Xiang GA, Xie X. Wang HN, et al. APMIS. 2014 May;122(5):443-51. doi: 10.1111/apm.12166. Epub 2013 Sep 11. APMIS. 2014. PMID: 24020820

8

The clinical spectrum of the m.10191T>C mutation in complex I-deficient Leigh syndrome.

Nesbitt V, Morrison PJ, Crushell E, Donnelly DE, Alston CL, He L, McFarland R, Taylor RW. Nesbitt V, et al. Dev Med Child Neurol. 2012 Jun;54(6):500-6. doi: 10.1111/j.1469-8749.2012.04224.x. Epub 2012 Feb 27. Dev Med Child Neurol. 2012. PMID: 22364517 Free article. Review.

9

Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutations.

Werner KG, Morel CF, Kirton A, Benseler SM, Shoffner JM, Addis JB, Robinson BH, Burrowes DM, Blaser SI, Epstein LG, Feigenbaum AS. Werner KG, et al. Pediatr Neurol. 2009 Jul;41(1):27-33. doi: 10.1016/j.pediatrneurol.2009.02.010. Pediatr Neurol. 2009. PMID: 19520270

10

Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystonia.

Wang K, Takahashi Y, Gao ZL, Wang GX, Chen XW, Goto J, Lou JN, Tsuji S. Wang K, et al. Neurogenetics. 2009 Oct;10(4):337-45. doi: 10.1007/s10048-009-0194-0. Epub 2009 May 21. Neurogenetics. 2009. PMID: 19458970

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