PubMed (OMIM) for id: 333240

Year	Number of Results
1956	1
1969	1
1970	1
1974	1
1978	1
1979	1
1980	1
1981	5
1982	4
1983	3
1984	2
1985	3
1986	7
1988	2
1989	5
1990	9
1991	11
1992	16
1993	16
1994	2
1996	2
1997	2
1998	2
1999	4
2000	3
2001	4
2002	7
2003	8
2004	5
2005	2
2024	0

1

A "Fille du Roy" introduced the T14484C Leber hereditary optic neuropathy mutation in French Canadians.

Laberge AM, Jomphe M, Houde L, Vezina H, Tremblay M, Desjardins B, Labuda D, St-Hilaire M, Macmillan C, Shoubridge EA, Brais B. Laberge AM, et al. Am J Hum Genet. 2005 Aug;77(2):313-7. doi: 10.1086/432491. Epub 2005 Jun 13. Am J Hum Genet. 2005. PMID: 15954041 Free PMC article.

2

Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD.

Pyle A, Foltynie T, Tiangyou W, Lambert C, Keers SM, Allcock LM, Davison J, Lewis SJ, Perry RH, Barker R, Burn DJ, Chinnery PF. Pyle A, et al. Ann Neurol. 2005 Apr;57(4):564-7. doi: 10.1002/ana.20417. Ann Neurol. 2005. PMID: 15786469

3

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

4

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

5

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.

6

NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency.

Kirby DM, Salemi R, Sugiana C, Ohtake A, Parry L, Bell KM, Kirk EP, Boneh A, Taylor RW, Dahl HH, Ryan MT, Thorburn DR. Kirby DM, et al. J Clin Invest. 2004 Sep;114(6):837-45. doi: 10.1172/JCI20683. J Clin Invest. 2004. PMID: 15372108 Free PMC article.

7

De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency.

McFarland R, Kirby DM, Fowler KJ, Ohtake A, Ryan MT, Amor DJ, Fletcher JM, Dixon JW, Collins FA, Turnbull DM, Taylor RW, Thorburn DR. McFarland R, et al. Ann Neurol. 2004 Jan;55(1):58-64. doi: 10.1002/ana.10787. Ann Neurol. 2004. PMID: 14705112

8

Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene.

Ugalde C, Triepels RH, Coenen MJ, van den Heuvel LP, Smeets R, Uusimaa J, Briones P, Campistol J, Majamaa K, Smeitink JA, Nijtmans LG. Ugalde C, et al. Ann Neurol. 2003 Nov;54(5):665-9. doi: 10.1002/ana.10734. Ann Neurol. 2003. PMID: 14595656

9

Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene.

Solano A, Roig M, Vives-Bauza C, Hernandez-Peña J, Garcia-Arumi E, Playan A, Lopez-Perez MJ, Andreu AL, Montoya J. Solano A, et al. Ann Neurol. 2003 Oct;54(4):527-30. doi: 10.1002/ana.10682. Ann Neurol. 2003. PMID: 14520668

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

131 results

Results by year