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Items: 1 to 20 of 105

1.

Xenogenic transfer of isolated murine mitochondria into human rho0 cells can improve respiratory function.

Katrangi E, D'Souza G, Boddapati SV, Kulawiec M, Singh KK, Bigger B, Weissig V.

Rejuvenation Res. 2007 Dec;10(4):561-70.

PMID:
18069915
2.

Internalization of isolated functional mitochondria: involvement of macropinocytosis.

Kitani T, Kami D, Matoba S, Gojo S.

J Cell Mol Med. 2014 Aug;18(8):1694-703. doi: 10.1111/jcmm.12316. Epub 2014 Jun 9.

3.
4.

Direct human mitochondrial transfer: a novel concept based on the endosymbiotic theory.

Kitani T, Kami D, Kawasaki T, Nakata M, Matoba S, Gojo S.

Transplant Proc. 2014 May;46(4):1233-6. doi: 10.1016/j.transproceed.2013.11.133.

PMID:
24815168
5.
6.

Functional and morphological abnormalities of mitochondria in human cells containing mitochondrial DNA with pathogenic point mutations in tRNA genes.

Hayashi J, Ohta S, Kagawa Y, Takai D, Miyabayashi S, Tada K, Fukushima H, Inui K, Okada S, Goto Y, et al.

J Biol Chem. 1994 Jul 22;269(29):19060-6.

7.

Inducible expression of a dominant negative DNA polymerase-gamma depletes mitochondrial DNA and produces a rho0 phenotype.

Jazayeri M, Andreyev A, Will Y, Ward M, Anderson CM, Clevenger W.

J Biol Chem. 2003 Mar 14;278(11):9823-30.

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9.

An update on the mitochondrial-DNA mutation hypothesis of cell aging.

Miquel J.

Mutat Res. 1992 Sep;275(3-6):209-16. Review.

PMID:
1383762
10.

Mitochondrial DNA mutations in mutator mice confer respiration defects and B-cell lymphoma development.

Mito T, Kikkawa Y, Shimizu A, Hashizume O, Katada S, Imanishi H, Ota A, Kato Y, Nakada K, Hayashi J.

PLoS One. 2013;8(2):e55789. doi: 10.1371/journal.pone.0055789. Epub 2013 Feb 13.

11.

Establishment of human cell lines lacking mitochondrial DNA.

Hashiguchi K, Zhang-Akiyama QM.

Methods Mol Biol. 2009;554:383-91. doi: 10.1007/978-1-59745-521-3_23.

PMID:
19513686
12.

Long-term postmortem survival of mitochondrial genomes in mouse synaptosomes and their rescue in a mitochondrial DNA-less mouse cell line.

Ito S, Inoue K, Yanagisawa N, Kaneko M, Hayashi J.

Biochem Biophys Res Commun. 1998 Jun 18;247(2):432-5.

PMID:
9642145
13.
14.

Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion.

Vielhaber S, Debska-Vielhaber G, Peeva V, Schoeler S, Kudin AP, Minin I, Schreiber S, Dengler R, Kollewe K, Zuschratter W, Kornblum C, Zsurka G, Kunz WS.

Acta Neuropathol. 2013 Feb;125(2):245-56. doi: 10.1007/s00401-012-1036-y. Epub 2012 Aug 28.

PMID:
22926664
15.

Presence of interaction but not complementation between human mtDNAs carrying different mutations within a tRNA(Leu(UUR)) gene.

Ono T, Kasahara Y, Nakada K, Hayashi JI.

Biochem Biophys Res Commun. 2004 Feb 20;314(4):1107-12.

PMID:
14751247
16.
17.

Cell and animal models of mtDNA biology: progress and prospects.

Khan SM, Smigrodzki RM, Swerdlow RH.

Am J Physiol Cell Physiol. 2007 Feb;292(2):C658-69. Epub 2006 Aug 9. Review.

18.

Cells depleted of mitochondrial DNA (rho0) yield insight into physiological mechanisms.

Chandel NS, Schumacker PT.

FEBS Lett. 1999 Jul 9;454(3):173-6. Review.

19.

Mitochondrial transfer between cells can rescue aerobic respiration.

Spees JL, Olson SD, Whitney MJ, Prockop DJ.

Proc Natl Acad Sci U S A. 2006 Jan 31;103(5):1283-8. Epub 2006 Jan 23.

20.

Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production.

Trifunovic A, Hansson A, Wredenberg A, Rovio AT, Dufour E, Khvorostov I, Spelbrink JN, Wibom R, Jacobs HT, Larsson NG.

Proc Natl Acad Sci U S A. 2005 Dec 13;102(50):17993-8. Epub 2005 Dec 6.

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