Fellman V - Search Results

1

Mitochondrial respiration in human viable platelets--methodology and influence of gender, age and storage.

Sjövall F, Ehinger JK, Marelsson SE, Morota S, Frostner EA, Uchino H, Lundgren J, Arnbjörnsson E, Hansson MJ, Fellman V, Elmér E. Sjövall F, et al. Among authors: fellman v. Mitochondrion. 2013 Jan;13(1):7-14. doi: 10.1016/j.mito.2012.11.001. Epub 2012 Nov 16. Mitochondrion. 2013. PMID: 23164798 Free article.

2

Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation.

Kotarsky H, Karikoski R, Mörgelin M, Marjavaara S, Bergman P, Zhang DL, Smet J, van Coster R, Fellman V. Kotarsky H, et al. Among authors: fellman v. Mitochondrion. 2010 Aug;10(5):497-509. doi: 10.1016/j.mito.2010.05.009. Epub 2010 May 23. Mitochondrion. 2010. PMID: 20580947

3

The GRACILE mutation introduced into Bcs1l causes postnatal complex III deficiency: a viable mouse model for mitochondrial hepatopathy.

Levéen P, Kotarsky H, Mörgelin M, Karikoski R, Elmér E, Fellman V. Levéen P, et al. Among authors: fellman v. Hepatology. 2011 Feb;53(2):437-47. doi: 10.1002/hep.24031. Epub 2010 Dec 28. Hepatology. 2011. PMID: 21274865

4

Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model.

Tegelberg S, Tomašić N, Kallijärvi J, Purhonen J, Elmér E, Lindberg E, Nord DG, Soller M, Lesko N, Wedell A, Bruhn H, Freyer C, Stranneheim H, Wibom R, Nennesmo I, Wredenberg A, Eklund EA, Fellman V. Tegelberg S, et al. Among authors: fellman v. Orphanet J Rare Dis. 2017 Apr 20;12(1):73. doi: 10.1186/s13023-017-0624-2. Orphanet J Rare Dis. 2017. PMID: 28427446 Free PMC article.

5

Oxygen consumption in platelets as an adjunct diagnostic method for pediatric mitochondrial disease.

Westerlund E, Marelsson SE, Ehinger JK, Sjövall F, Morota S, Åsander Frostner E, Oldfors A, Darin N, Lundgren J, Hansson MJ, Fellman V, Elmér E. Westerlund E, et al. Among authors: fellman v. Pediatr Res. 2018 Feb;83(2):455-465. doi: 10.1038/pr.2017.250. Epub 2017 Nov 15. Pediatr Res. 2018. PMID: 28981487

6

Fasting reveals largely intact systemic lipid mobilization mechanisms in respiratory chain complex III deficient mice.

Tomašić N, Kotarsky H, de Oliveira Figueiredo R, Hansson E, Mörgelin M, Tomašić I, Kallijärvi J, Elmér E, Jauhiainen M, Eklund EA, Fellman V. Tomašić N, et al. Among authors: fellman v. Biochim Biophys Acta Mol Basis Dis. 2020 Jan 1;1866(1):165573. doi: 10.1016/j.bbadis.2019.165573. Epub 2019 Oct 29. Biochim Biophys Acta Mol Basis Dis. 2020. PMID: 31672551 Free article.

7

Mitochondrial hepatopathies in the newborn period.

Fellman V, Kotarsky H. Fellman V, et al. Semin Fetal Neonatal Med. 2011 Aug;16(4):222-8. doi: 10.1016/j.siny.2011.05.002. Epub 2011 Jun 15. Semin Fetal Neonatal Med. 2011. PMID: 21680270 Review.

8

The radical-binding lipocalin A1M binds to a Complex I subunit and protects mitochondrial structure and function.

Olsson MG, Rosenlöf LW, Kotarsky H, Olofsson T, Leanderson T, Mörgelin M, Fellman V, Åkerström B. Olsson MG, et al. Among authors: fellman v. Antioxid Redox Signal. 2013 Jun 1;18(16):2017-28. doi: 10.1089/ars.2012.4658. Epub 2013 Jan 4. Antioxid Redox Signal. 2013. PMID: 23157686

9

Complex I function and supercomplex formation are preserved in liver mitochondria despite progressive complex III deficiency.

Davoudi M, Kotarsky H, Hansson E, Fellman V. Davoudi M, et al. Among authors: fellman v. PLoS One. 2014 Jan 22;9(1):e86767. doi: 10.1371/journal.pone.0086767. eCollection 2014. PLoS One. 2014. PMID: 24466228 Free PMC article.

10

A mouse model of mitochondrial complex III dysfunction induced by myxothiazol.

Davoudi M, Kallijärvi J, Marjavaara S, Kotarsky H, Hansson E, Levéen P, Fellman V. Davoudi M, et al. Among authors: fellman v. Biochem Biophys Res Commun. 2014 Apr 18;446(4):1079-84. doi: 10.1016/j.bbrc.2014.03.058. Epub 2014 Mar 21. Biochem Biophys Res Commun. 2014. PMID: 24661880

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