Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

28 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO.
Greaves LC, Yu-Wai-Man P, Blakely EL, Krishnan KJ, Beadle NE, Kerin J, Barron MJ, Griffiths PG, Dickinson AJ, Turnbull DM, Taylor RW. Greaves LC, et al. Among authors: krishnan kj. Invest Ophthalmol Vis Sci. 2010 Jul;51(7):3340-6. doi: 10.1167/iovs.09-4659. Epub 2010 Feb 17. Invest Ophthalmol Vis Sci. 2010. PMID: 20164463 Free PMC article.
Detection of mitochondrial DNA variation in human cells.
Krishnan KJ, Blackwood JK, Reeve AK, Turnbull DM, Taylor RW. Krishnan KJ, et al. Methods Mol Biol. 2010;628:227-57. doi: 10.1007/978-1-60327-367-1_13. Methods Mol Biol. 2010. PMID: 20238085
Mitochondrial DNA mutations and aging.
Krishnan KJ, Greaves LC, Reeve AK, Turnbull DM. Krishnan KJ, et al. Ann N Y Acad Sci. 2007 Apr;1100:227-40. doi: 10.1196/annals.1395.024. Ann N Y Acad Sci. 2007. PMID: 17460184 Review.
What causes mitochondrial DNA deletions in human cells?
Krishnan KJ, Reeve AK, Samuels DC, Chinnery PF, Blackwood JK, Taylor RW, Wanrooij S, Spelbrink JN, Lightowlers RN, Turnbull DM. Krishnan KJ, et al. Nat Genet. 2008 Mar;40(3):275-9. doi: 10.1038/ng.f.94. Nat Genet. 2008. PMID: 18305478 Review.
Late-onset respiratory failure due to TK2 mutations causing multiple mtDNA deletions.
Alston CL, Schaefer AM, Raman P, Solaroli N, Krishnan KJ, Blakely EL, He L, Craig K, Roberts M, Vyas A, Nixon J, Horvath R, Turnbull DM, Karlsson A, Gorman GS, Taylor RW. Alston CL, et al. Among authors: krishnan kj. Neurology. 2013 Dec 3;81(23):2051-3. doi: 10.1212/01.wnl.0000436931.94291.e6. Epub 2013 Nov 6. Neurology. 2013. PMID: 24198295 Free PMC article.
28 results