Thoms S - Search Results

1

Bulankina AV, Thoms S. Bulankina AV, et al. Among authors: thoms s. Cells. 2020 Feb 25;9(3):534. doi: 10.3390/cells9030534. Cells. 2020. PMID: 32106631 Free PMC article. Review.

2

Dysferlin mediates membrane tubulation and links T-tubule biogenesis to muscular dystrophy.

Hofhuis J, Bersch K, Büssenschütt R, Drzymalski M, Liebetanz D, Nikolaev VO, Wagner S, Maier LS, Gärtner J, Klinge L, Thoms S. Hofhuis J, et al. Among authors: thoms s. J Cell Sci. 2017 Mar 1;130(5):841-852. doi: 10.1242/jcs.198861. Epub 2017 Jan 19. J Cell Sci. 2017. PMID: 28104817

3

Dysferlin links excitation-contraction coupling to structure and maintenance of the cardiac transverse-axial tubule system.

Hofhuis J, Bersch K, Wagner S, Molina C, Fakuade FE, Iyer LM, Streckfuss-Bömeke K, Toischer K, Zelarayán LC, Voigt N, Nikolaev VO, Maier LS, Klinge L, Thoms S. Hofhuis J, et al. Among authors: thoms s. Europace. 2020 Jul 1;22(7):1119-1131. doi: 10.1093/europace/euaa093. Europace. 2020. PMID: 32572487

4

Functional Translational Readthrough: A Systems Biology Perspective.

Schueren F, Thoms S. Schueren F, et al. Among authors: thoms s. PLoS Genet. 2016 Aug 4;12(8):e1006196. doi: 10.1371/journal.pgen.1006196. eCollection 2016 Aug. PLoS Genet. 2016. PMID: 27490485 Free PMC article. Review.

5

RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection.

Henneke M, Diekmann S, Ohlenbusch A, Kaiser J, Engelbrecht V, Kohlschütter A, Krätzner R, Madruga-Garrido M, Mayer M, Opitz L, Rodriguez D, Rüschendorf F, Schumacher J, Thiele H, Thoms S, Steinfeld R, Nürnberg P, Gärtner J. Henneke M, et al. Among authors: thoms s. Nat Genet. 2009 Jul;41(7):773-5. doi: 10.1038/ng.398. Epub 2009 Jun 14. Nat Genet. 2009. PMID: 19525954

6

Organelle interplay in peroxisomal disorders.

Thoms S, Grønborg S, Gärtner J. Thoms S, et al. Trends Mol Med. 2009 Jul;15(7):293-302. doi: 10.1016/j.molmed.2009.05.002. Epub 2009 Jun 26. Trends Mol Med. 2009. PMID: 19560974 Review.

7

The unusual extended C-terminal helix of the peroxisomal α/β-hydrolase Lpx1 is involved in dimer contacts but dispensable for dimerization.

Thoms S, Hofhuis J, Thöing C, Gärtner J, Niemann HH. Thoms S, et al. J Struct Biol. 2011 Sep;175(3):362-71. doi: 10.1016/j.jsb.2011.06.008. Epub 2011 Jun 29. J Struct Biol. 2011. PMID: 21741480

8

Characterization of two common 5' polymorphisms in PEX1 and correlation to survival in PEX1 peroxisome biogenesis disorder patients.

Thoms S, Grønborg S, Rabenau J, Ohlenbusch A, Rosewich H, Gärtner J. Thoms S, et al. BMC Med Genet. 2011 Aug 16;12:109. doi: 10.1186/1471-2350-12-109. BMC Med Genet. 2011. PMID: 21846392 Free PMC article.

9

Peroxisome formation requires the endoplasmic reticulum channel protein Sec61.

Thoms S, Harms I, Kalies KU, Gärtner J. Thoms S, et al. Traffic. 2012 Apr;13(4):599-609. doi: 10.1111/j.1600-0854.2011.01324.x. Epub 2012 Jan 17. Traffic. 2012. PMID: 22212716 Free article.

10

First PEX11β patient extends spectrum of peroxisomal biogenesis disorder phenotypes.

Thoms S, Gärtner J. Thoms S, et al. J Med Genet. 2012 May;49(5):314-6. doi: 10.1136/jmedgenet-2012-100899. J Med Genet. 2012. PMID: 22581969

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

103 results

Search Page