Similar articles for PMID: 18276892

Year	Number of Results
1994	5
1995	5
1996	2
1997	2
1998	4
1999	3
2000	7
2001	4
2002	3
2003	2
2004	5
2005	3
2006	4
2007	1
2008	9
2009	3
2010	2
2011	1
2012	5
2013	5
2014	8
2015	7
2016	2
2018	6
2019	3
2020	4
2021	4
2023	1
2024	0

1

A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations.

Fan W, Waymire KG, Narula N, Li P, Rocher C, Coskun PE, Vannan MA, Narula J, Macgregor GR, Wallace DC. Fan W, et al. Science. 2008 Feb 15;319(5865):958-62. doi: 10.1126/science.1147786. Science. 2008. PMID: 18276892 Free PMC article.

2

Medicine. Sidestepping mutational meltdown.

Shoubridge EA, Wai T. Shoubridge EA, et al. Science. 2008 Feb 15;319(5865):914-5. doi: 10.1126/science.1154515. Science. 2008. PMID: 18276880 No abstract available.

3

The pattern of natural selection in somatic cancer mutations of human mtDNA.

Stafford P, Chen-Quin EB. Stafford P, et al. J Hum Genet. 2010 Sep;55(9):605-12. doi: 10.1038/jhg.2010.76. Epub 2010 Jul 8. J Hum Genet. 2010. PMID: 20613764

4

Novel heteroplasmic frameshift and missense somatic mitochondrial DNA mutations in oral cancer of betel quid chewers.

Tan DJ, Chang J, Chen WL, Agress LJ, Yeh KT, Wang B, Wong LJ. Tan DJ, et al. Genes Chromosomes Cancer. 2003 Jun;37(2):186-94. doi: 10.1002/gcc.10217. Genes Chromosomes Cancer. 2003. PMID: 12696067

5

The mtDNA-encoded ND6 subunit of mitochondrial NADH dehydrogenase is essential for the assembly of the membrane arm and the respiratory function of the enzyme.

Bai Y, Attardi G. Bai Y, et al. EMBO J. 1998 Aug 17;17(16):4848-58. doi: 10.1093/emboj/17.16.4848. EMBO J. 1998. PMID: 9707444 Free PMC article.

6

Mutation-specific effects in germline transmission of pathogenic mtDNA variants.

Otten ABC, Sallevelt SCEH, Carling PJ, Dreesen JCFM, Drüsedau M, Spierts S, Paulussen ADC, de Die-Smulders CEM, Herbert M, Chinnery PF, Samuels DC, Lindsey P, Smeets HJM. Otten ABC, et al. Hum Reprod. 2018 Jul 1;33(7):1331-1341. doi: 10.1093/humrep/dey114. Hum Reprod. 2018. PMID: 29850888 Free PMC article.

7

Inherited pathogenic mitochondrial DNA mutations and gastrointestinal stem cell populations.

Su T, Grady JP, Afshar S, McDonald SA, Taylor RW, Turnbull DM, Greaves LC. Su T, et al. J Pathol. 2018 Dec;246(4):427-432. doi: 10.1002/path.5156. Epub 2018 Nov 5. J Pathol. 2018. PMID: 30146801 Free PMC article.

8

Deleterious mtDNA mutations are common in mature oocytes.

Ma H, Hayama T, Van Dyken C, Darby H, Koski A, Lee Y, Gutierrez NM, Yamada S, Li Y, Andrews M, Ahmed R, Liang D, Gonmanee T, Kang E, Nasser M, Kempton B, Brigande J, McGill TJ, Terzic A, Amato P, Mitalipov S. Ma H, et al. Biol Reprod. 2020 Mar 13;102(3):607-619. doi: 10.1093/biolre/ioz202. Biol Reprod. 2020. PMID: 31621839 Free PMC article.

9

Nuclear suppression of mitochondrial defects in cells without the ND6 subunit.

Deng JH, Li Y, Park JS, Wu J, Hu P, Lechleiter J, Bai Y. Deng JH, et al. Mol Cell Biol. 2006 Feb;26(3):1077-86. doi: 10.1128/MCB.26.3.1077-1086.2006. Mol Cell Biol. 2006. PMID: 16428459 Free PMC article.

10

A patient with two mitochondrial DNA mutations causing PEO and LHON.

Melberg A, Moslemi AR, Palm O, Raininko R, Stålberg E, Oldfors A. Melberg A, et al. Eur J Med Genet. 2009 Jan-Feb;52(1):47-8. doi: 10.1016/j.ejmg.2008.10.004. Epub 2008 Nov 5. Eur J Med Genet. 2009. PMID: 19015050

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