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

My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1997 1
1998 2
2000 1
2002 2
2003 2
2004 3
2005 1
2006 3
2007 5
2008 3
2009 4
2010 1
2011 1
2012 3
2013 2
2014 2
2015 1
2016 1
2017 2
2018 1
2020 1
2021 1
2023 0
Text availability
Article attribute
Article type
Publication date

Search Results

35 results
Results by year
Filters applied: . Clear all
Page 1
Mitochondrial involvement in temporal lobe epilepsy.
Kudin AP, Zsurka G, Elger CE, Kunz WS. Kudin AP, et al. Exp Neurol. 2009 Aug;218(2):326-32. doi: 10.1016/j.expneurol.2009.02.014. Epub 2009 Mar 5. Exp Neurol. 2009. PMID: 19268667 Review.
Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy.
Kudin AP, Baron G, Zsurka G, Hampel KG, Elger CE, Grote A, Weber Y, Lerche H, Thiele H, Nürnberg P, Schulz H, Ruppert AK, Sander T, Cheng Q, Arnér ES, Schomburg L, Seeher S, Fradejas-Villar N, Schweizer U, Kunz WS. Kudin AP, et al. Free Radic Biol Med. 2017 May;106:270-277. doi: 10.1016/j.freeradbiomed.2017.02.040. Epub 2017 Feb 21. Free Radic Biol Med. 2017. PMID: 28232204
Heart failure after pressure overload in autosomal-dominant desminopathies: Lessons from heterozygous DES-p.R349P knock-in mice.
Stöckigt F, Eichhorn L, Beiert T, Knappe V, Radecke T, Steinmetz M, Nickenig G, Peeva V, Kudin AP, Kunz WS, Berwanger C, Kamm L, Schultheis D, Schlötzer-Schrehardt U, Clemen CS, Schröder R, Schrickel JW. Stöckigt F, et al. Among authors: kudin ap. PLoS One. 2020 Mar 3;15(3):e0228913. doi: 10.1371/journal.pone.0228913. eCollection 2020. PLoS One. 2020. PMID: 32126091 Free PMC article.
Loss of UCP2 attenuates mitochondrial dysfunction without altering ROS production and uncoupling activity.
Kukat A, Dogan SA, Edgar D, Mourier A, Jacoby C, Maiti P, Mauer J, Becker C, Senft K, Wibom R, Kudin AP, Hultenby K, Flögel U, Rosenkranz S, Ricquier D, Kunz WS, Trifunovic A. Kukat A, et al. Among authors: kudin ap. PLoS Genet. 2014 Jun 19;10(6):e1004385. doi: 10.1371/journal.pgen.1004385. eCollection 2014 Jun. PLoS Genet. 2014. PMID: 24945157 Free PMC article.
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. Vielhaber S, et al. Among authors: kudin ap. Acta Neuropathol. 2013 Feb;125(2):245-56. doi: 10.1007/s00401-012-1036-y. Epub 2012 Aug 28. Acta Neuropathol. 2013. PMID: 22926664
35 results