Wredenberg A - Search Results

1

Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3.

Ben-Shabat I, Kvarnung M, Sperker W, Bruhn H, Wredenberg A, Wibom R, Nennesmo I, Engvall M, Paucar M. Ben-Shabat I, et al. Among authors: wredenberg a. Neurol Genet. 2023 Nov 28;9(6):e200100. doi: 10.1212/NXG.0000000000200100. eCollection 2023 Dec. Neurol Genet. 2023. PMID: 38035175 Free PMC article.

2

An international classification of inherited metabolic disorders (ICIMD).

Ferreira CR, Rahman S, Keller M, Zschocke J; ICIMD Advisory Group. Ferreira CR, et al. J Inherit Metab Dis. 2021 Jan;44(1):164-177. doi: 10.1002/jimd.12348. J Inherit Metab Dis. 2021. PMID: 33340416 Free PMC article.

3

Increased mitochondrial Ca2+ and decreased sarcoplasmic reticulum Ca2+ in mitochondrial myopathy.

Aydin J, Andersson DC, Hänninen SL, Wredenberg A, Tavi P, Park CB, Larsson NG, Bruton JD, Westerblad H. Aydin J, et al. Among authors: wredenberg a. Hum Mol Genet. 2009 Jan 15;18(2):278-88. doi: 10.1093/hmg/ddn355. Epub 2008 Oct 22. Hum Mol Genet. 2009. PMID: 18945718

4

Complementation between polymerase- and exonuclease-deficient mitochondrial DNA polymerase mutants in genomically engineered flies.

Bratic A, Kauppila TE, Macao B, Grönke S, Siibak T, Stewart JB, Baggio F, Dols J, Partridge L, Falkenberg M, Wredenberg A, Larsson NG. Bratic A, et al. Among authors: wredenberg a. Nat Commun. 2015 Nov 10;6:8808. doi: 10.1038/ncomms9808. Nat Commun. 2015. PMID: 26554610 Free PMC article.

5

Increased mitochondrial mass in mitochondrial myopathy mice.

Wredenberg A, Wibom R, Wilhelmsson H, Graff C, Wiener HH, Burden SJ, Oldfors A, Westerblad H, Larsson NG. Wredenberg A, et al. Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):15066-71. doi: 10.1073/pnas.232591499. Epub 2002 Nov 4. Proc Natl Acad Sci U S A. 2002. PMID: 12417746 Free PMC article.

6

Premature ageing in mice expressing defective mitochondrial DNA polymerase.

Trifunovic A, Wredenberg A, Falkenberg M, Spelbrink JN, Rovio AT, Bruder CE, Bohlooly-Y M, Gidlöf S, Oldfors A, Wibom R, Törnell J, Jacobs HT, Larsson NG. Trifunovic A, et al. Among authors: wredenberg a. Nature. 2004 May 27;429(6990):417-23. doi: 10.1038/nature02517. Nature. 2004. PMID: 15164064

7

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. Trifunovic A, et al. Among authors: wredenberg a. Proc Natl Acad Sci U S A. 2005 Dec 13;102(50):17993-8. doi: 10.1073/pnas.0508886102. Epub 2005 Dec 6. Proc Natl Acad Sci U S A. 2005. PMID: 16332961 Free PMC article.

8

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. 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

9

The bicoid stability factor controls polyadenylation and expression of specific mitochondrial mRNAs in Drosophila melanogaster.

Bratic A, Wredenberg A, Grönke S, Stewart JB, Mourier A, Ruzzenente B, Kukat C, Wibom R, Habermann B, Partridge L, Larsson NG. Bratic A, et al. Among authors: wredenberg a. PLoS Genet. 2011 Oct;7(10):e1002324. doi: 10.1371/journal.pgen.1002324. Epub 2011 Oct 13. PLoS Genet. 2011. PMID: 22022283 Free PMC article.

10

Rapid pulsed whole genome sequencing for comprehensive acute diagnostics of inborn errors of metabolism.

Stranneheim H, Engvall M, Naess K, Lesko N, Larsson P, Dahlberg M, Andeer R, Wredenberg A, Freyer C, Barbaro M, Bruhn H, Emahazion T, Magnusson M, Wibom R, Zetterström RH, Wirta V, von Döbeln U, Wedell A. Stranneheim H, et al. Among authors: wredenberg a. BMC Genomics. 2014 Dec 11;15(1):1090. doi: 10.1186/1471-2164-15-1090. BMC Genomics. 2014. PMID: 25495354 Free PMC article.

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