Freyer C - Search Results

1

TWINKLE is an essential mitochondrial helicase required for synthesis of nascent D-loop strands and complete mtDNA replication.

Milenkovic D, Matic S, Kühl I, Ruzzenente B, Freyer C, Jemt E, Park CB, Falkenberg M, Larsson NG. Milenkovic D, et al. Among authors: freyer c. Hum Mol Genet. 2013 May 15;22(10):1983-93. doi: 10.1093/hmg/ddt051. Epub 2013 Feb 7. Hum Mol Genet. 2013. PMID: 23393161 Free PMC article.

2

The influence of intravenous L-tryptophan on plasma melatonin and sleep in men.

Hajak G, Huether G, Blanke J, Blömer M, Freyer C, Poeggeler B, Reimer A, Rodenbeck A, Schulz-Varszegi M, Rüther E. Hajak G, et al. Among authors: freyer c. Pharmacopsychiatry. 1991 Jan;24(1):17-20. doi: 10.1055/s-2007-1014427. Pharmacopsychiatry. 1991. PMID: 2011617 Clinical Trial.

3

Respiratory chain dysfunction in skeletal muscle does not cause insulin resistance.

Wredenberg A, Freyer C, Sandström ME, Katz A, Wibom R, Westerblad H, Larsson NG. Wredenberg A, et al. Among authors: freyer c. Biochem Biophys Res Commun. 2006 Nov 10;350(1):202-7. doi: 10.1016/j.bbrc.2006.09.029. Epub 2006 Sep 18. Biochem Biophys Res Commun. 2006. PMID: 16996481

4

Is energy deficiency good in moderation?

Freyer C, Larsson NG. Freyer C, et al. Cell. 2007 Nov 2;131(3):448-50. doi: 10.1016/j.cell.2007.10.027. Cell. 2007. PMID: 17981112 Free article.

5

Strong purifying selection in transmission of mammalian mitochondrial DNA.

Stewart JB, Freyer C, Elson JL, Wredenberg A, Cansu Z, Trifunovic A, Larsson NG. Stewart JB, et al. Among authors: freyer c. PLoS Biol. 2008 Jan;6(1):e10. doi: 10.1371/journal.pbio.0060010. PLoS Biol. 2008. PMID: 18232733 Free PMC article.

6

Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease.

Stewart JB, Freyer C, Elson JL, Larsson NG. Stewart JB, et al. Among authors: freyer c. Nat Rev Genet. 2008 Sep;9(9):657-62. doi: 10.1038/nrg2396. Nat Rev Genet. 2008. PMID: 18695671 Review.

7

MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome.

Naess K, Freyer C, Bruhn H, Wibom R, Malm G, Nennesmo I, von Döbeln U, Larsson NG. Naess K, et al. Among authors: freyer c. Biochim Biophys Acta. 2009 May;1787(5):484-90. doi: 10.1016/j.bbabio.2008.11.014. Epub 2008 Dec 6. Biochim Biophys Acta. 2009. PMID: 19103152 Free article.

8

Maintenance of respiratory chain function in mouse hearts with severely impaired mtDNA transcription.

Freyer C, Park CB, Ekstrand MI, Shi Y, Khvorostova J, Wibom R, Falkenberg M, Gustafsson CM, Larsson NG. Freyer C, et al. Nucleic Acids Res. 2010 Oct;38(19):6577-88. doi: 10.1093/nar/gkq527. Epub 2010 Jun 20. Nucleic Acids Res. 2010. PMID: 20566479 Free PMC article.

9

Ultra-deep sequencing of mouse mitochondrial DNA: mutational patterns and their origins.

Ameur A, Stewart JB, Freyer C, Hagström E, Ingman M, Larsson NG, Gyllensten U. Ameur A, et al. Among authors: freyer c. PLoS Genet. 2011 Mar;7(3):e1002028. doi: 10.1371/journal.pgen.1002028. Epub 2011 Mar 24. PLoS Genet. 2011. PMID: 21455489 Free PMC article.

10

Variation in germline mtDNA heteroplasmy is determined prenatally but modified during subsequent transmission.

Freyer C, Cree LM, Mourier A, Stewart JB, Koolmeister C, Milenkovic D, Wai T, Floros VI, Hagström E, Chatzidaki EE, Wiesner RJ, Samuels DC, Larsson NG, Chinnery PF. Freyer C, et al. Nat Genet. 2012 Nov;44(11):1282-5. doi: 10.1038/ng.2427. Epub 2012 Oct 7. Nat Genet. 2012. PMID: 23042113 Free PMC article.

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