PubMed (cited) for id: 516000

Year	Number of Results
1956	1
1974	1
1979	1
1980	1
1981	5
1982	4
1983	2
1984	2
1985	2
1986	4
1990	2
1991	5
1992	10
1993	2
1998	1
1999	3
2000	1
2002	4
2003	1
2004	3
2006	2
2007	3
2012	1
2024	0

1

Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss.

Gutiérrez Cortés N, Pertuiset C, Dumon E, Börlin M, Hebert-Chatelain E, Pierron D, Feldmann D, Jonard L, Marlin S, Letellier T, Rocher C. Gutiérrez Cortés N, et al. Hum Mutat. 2012 Apr;33(4):681-9. doi: 10.1002/humu.22023. Epub 2012 Feb 14. Hum Mutat. 2012. PMID: 22241583

2

Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.

Lévêque M, Marlin S, Jonard L, Procaccio V, Reynier P, Amati-Bonneau P, Baulande S, Pierron D, Lacombe D, Duriez F, Francannet C, Mom T, Journel H, Catros H, Drouin-Garraud V, Obstoy MF, Dollfus H, Eliot MM, Faivre L, Duvillard C, Couderc R, Garabedian EN, Petit C, Feldmann D, Denoyelle F. Lévêque M, et al. Eur J Hum Genet. 2007 Nov;15(11):1145-55. doi: 10.1038/sj.ejhg.5201891. Epub 2007 Jul 18. Eur J Hum Genet. 2007. PMID: 17637808

3

Primary spinal cord neurodegeneration in Leber hereditary optic neuropathy.

Jaros E, Mahad DJ, Hudson G, Birchall D, Sawcer SJ, Griffiths PG, Sunter J, Compston DA, Perry RH, Chinnery PF. Jaros E, et al. Neurology. 2007 Jul 10;69(2):214-6. doi: 10.1212/01.wnl.0000265598.76172.59. Neurology. 2007. PMID: 17620555 No abstract available.

4

A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystonia.

Spruijt L, Smeets HJ, Hendrickx A, Bettink-Remeijer MW, Maat-Kievit A, Schoonderwoerd KC, Sluiter W, de Coo IF, Hintzen RQ. Spruijt L, et al. Arch Neurol. 2007 Jun;64(6):890-3. doi: 10.1001/archneur.64.6.890. Arch Neurol. 2007. PMID: 17562939

5

Analysis of mitochondrial DNA sequences in patients with isolated or combined oxidative phosphorylation system deficiency.

Hinttala R, Smeets R, Moilanen JS, Ugalde C, Uusimaa J, Smeitink JA, Majamaa K. Hinttala R, et al. J Med Genet. 2006 Nov;43(11):881-6. doi: 10.1136/jmg.2006.042168. Epub 2006 May 31. J Med Genet. 2006. PMID: 16738010 Free PMC article.

6

Sporadic intragenic inversion of the mitochondrial DNA MTND1 gene causing fatal infantile lactic acidosis.

Blakely EL, Rennie KJ, Jones L, Elstner M, Chrzanowska-Lightowlers ZM, White CB, Shield JP, Pilz DT, Turnbull DM, Poulton J, Taylor RW. Blakely EL, et al. Pediatr Res. 2006 Mar;59(3):440-4. doi: 10.1203/01.pdr.0000198771.78290.c4. Pediatr Res. 2006. PMID: 16492986

7

Mitochondrial DNA 3644T-->C mutation associated with bipolar disorder.

Munakata K, Tanaka M, Mori K, Washizuka S, Yoneda M, Tajima O, Akiyama T, Nanko S, Kunugi H, Tadokoro K, Ozaki N, Inada T, Sakamoto K, Fukunaga T, Iijima Y, Iwata N, Tatsumi M, Yamada K, Yoshikawa T, Kato T. Munakata K, et al. Genomics. 2004 Dec;84(6):1041-50. doi: 10.1016/j.ygeno.2004.08.015. Genomics. 2004. PMID: 15533721

8

The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy.

Valentino ML, Barboni P, Ghelli A, Bucchi L, Rengo C, Achilli A, Torroni A, Lugaresi A, Lodi R, Barbiroli B, Dotti M, Federico A, Baruzzi A, Carelli V. Valentino ML, et al. Ann Neurol. 2004 Nov;56(5):631-41. doi: 10.1002/ana.20236. Ann Neurol. 2004. PMID: 15505787

9

Mutations of the mitochondrial ND1 gene as a cause of MELAS.

Kirby DM, McFarland R, Ohtake A, Dunning C, Ryan MT, Wilson C, Ketteridge D, Turnbull DM, Thorburn DR, Taylor RW. Kirby DM, et al. J Med Genet. 2004 Oct;41(10):784-9. doi: 10.1136/jmg.2004.020537. J Med Genet. 2004. PMID: 15466014 Free PMC article. No abstract available.

10

On the origin of cancer cells.

WARBURG O. WARBURG O. Science. 1956 Feb 24;123(3191):309-14. doi: 10.1126/science.123.3191.309. Science. 1956. PMID: 13298683 No abstract available.

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