Roos A - Search Results

1

Biochemical and pathological changes result from mutated Caveolin-3 in muscle.

González Coraspe JA, Weis J, Anderson ME, Münchberg U, Lorenz K, Buchkremer S, Carr S, Zahedi RP, Brauers E, Michels H, Sunada Y, Lochmüller H, Campbell KP, Freier E, Hathazi D, Roos A. González Coraspe JA, et al. Among authors: roos a. Skelet Muscle. 2018 Aug 28;8(1):28. doi: 10.1186/s13395-018-0173-y. Skelet Muscle. 2018. PMID: 30153853 Free PMC article.

2

Differential effects of myopathy-associated caveolin-3 mutants on growth factor signaling.

Brauers E, Dreier A, Roos A, Wormland B, Weis J, Krüttgen A. Brauers E, et al. Among authors: roos a. Am J Pathol. 2010 Jul;177(1):261-70. doi: 10.2353/ajpath.2010.090741. Epub 2010 May 14. Am J Pathol. 2010. PMID: 20472890 Free PMC article.

3

Novel FHL1 mutation in a family with reducing body myopathy.

Schreckenbach T, Henn W, Kress W, Roos A, Maschke M, Feiden W, Dillmann U, Schulz JB, Weis J, Claeys KG. Schreckenbach T, et al. Among authors: roos a. Muscle Nerve. 2013 Jan;47(1):127-34. doi: 10.1002/mus.23500. Epub 2012 Nov 21. Muscle Nerve. 2013. PMID: 23169582

4

Altered localization, abnormal modification and loss of function of Sigma receptor-1 in amyotrophic lateral sclerosis.

Prause J, Goswami A, Katona I, Roos A, Schnizler M, Bushuven E, Dreier A, Buchkremer S, Johann S, Beyer C, Deschauer M, Troost D, Weis J. Prause J, et al. Among authors: roos a. Hum Mol Genet. 2013 Apr 15;22(8):1581-600. doi: 10.1093/hmg/ddt008. Epub 2013 Jan 11. Hum Mol Genet. 2013. PMID: 23314020

5

Myopathy in Marinesco-Sjögren syndrome links endoplasmic reticulum chaperone dysfunction to nuclear envelope pathology.

Roos A, Buchkremer S, Kollipara L, Labisch T, Gatz C, Zitzelsberger M, Brauers E, Nolte K, Schröder JM, Kirschner J, Jesse CM, Goebel HH, Goswami A, Zimmermann R, Zahedi RP, Senderek J, Weis J. Roos A, et al. Acta Neuropathol. 2014 May;127(5):761-77. doi: 10.1007/s00401-013-1224-4. Epub 2013 Dec 21. Acta Neuropathol. 2014. PMID: 24362440

6

Marinesco-Sjögren syndrome protein SIL1 regulates motor neuron subtype-selective ER stress in ALS.

Filézac de L'Etang A, Maharjan N, Cordeiro Braña M, Ruegsegger C, Rehmann R, Goswami A, Roos A, Troost D, Schneider BL, Weis J, Saxena S. Filézac de L'Etang A, et al. Among authors: roos a. Nat Neurosci. 2015 Feb;18(2):227-38. doi: 10.1038/nn.3903. Epub 2015 Jan 5. Nat Neurosci. 2015. PMID: 25559081

7

Inverted formin 2-related Charcot-Marie-Tooth disease: extension of the mutational spectrum and pathological findings in Schwann cells and axons.

Roos A, Weis J, Korinthenberg R, Fehrenbach H, Häusler M, Züchner S, Mache C, Hubmann H, Auer-Grumbach M, Senderek J. Roos A, et al. J Peripher Nerv Syst. 2015 Mar;20(1):52-9. doi: 10.1111/jns.12106. J Peripher Nerv Syst. 2015. PMID: 25676889

8

Cellular Signature of SIL1 Depletion: Disease Pathogenesis due to Alterations in Protein Composition Beyond the ER Machinery.

Roos A, Kollipara L, Buchkremer S, Labisch T, Brauers E, Gatz C, Lentz C, Gerardo-Nava J, Weis J, Zahedi RP. Roos A, et al. Mol Neurobiol. 2016 Oct;53(8):5527-41. doi: 10.1007/s12035-015-9456-z. Epub 2015 Oct 14. Mol Neurobiol. 2016. PMID: 26468156

9

Proteome Profiling and Ultrastructural Characterization of the Human RCMH Cell Line: Myoblastic Properties and Suitability for Myopathological Studies.

Kollipara L, Buchkremer S, Weis J, Brauers E, Hoss M, Rütten S, Caviedes P, Zahedi RP, Roos A. Kollipara L, et al. Among authors: roos a. J Proteome Res. 2016 Mar 4;15(3):945-55. doi: 10.1021/acs.jproteome.5b00972. Epub 2016 Feb 15. J Proteome Res. 2016. PMID: 26781476

10

The Caveolin-3 G56S sequence variant of unknown significance: Muscle biopsy findings and functional cell biological analysis.

Brauers E, Roos A, Kollipara L, Zahedi RP, Beckmann A, Mohanadas N, Bauer H, Häusler M, Thoma S, Kress W, Senderek J, Weis J. Brauers E, et al. Among authors: roos a. Proteomics Clin Appl. 2017 Jan;11(1-2):1600007. doi: 10.1002/prca.201600007. Epub 2016 Nov 14. Proteomics Clin Appl. 2017. PMID: 27739254 Free PMC article.

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