Cookies help us deliver our services. By using our services, you agree to our use of cookies. More information

Difference between revisions of "Soller M"

From Bioblast
 
 
Line 1: Line 1:
{{Person}}
{{Person}}
{{Labelingperson}}

Latest revision as of 15:05, 30 November 2016

Name ,
Institution
Address ,
City
State/Province
Country
Email
Weblink
O2k-Network Lab


Labels:



Publications

 PublishedReference
Tegelberg 2017 Orphanet J Rare Dis2017Tegelberg 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 (2017) Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model. Orphanet J Rare Dis 12:73.
Soller 2007 Mol Pharmacol2007Soller M, Dröse S, Brandt U, Brüne B, von Knethen A (2007) Mechanism of Thiazolidinedione-dependent cell death in Jurkat T cells. Mol Pharmacol 71:1535-44.

Abstracts

Add abstract