Publications by authors named "Eva Brauers"

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Biochemical and pathological changes result from mutated Caveolin-3 in muscle.
José Andrés González Coraspe, Joachim Weis, Mary E Anderson, Ute Münchberg, Kristina Lorenz, Eva Brauers

Skelet Muscle· August 2018

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The Caveolin-3 G56S sequence variant of unknown significance: Muscle biopsy findings and functional cell biological analysis.
Eva Brauers, Andreas Roos, Laxmikanth Kollipara, René P Zahedi, Alf Beckmann

Proteomics Clin Appl· January 2017

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Cellular Signature of SIL1 Depletion: Disease Pathogenesis due to Alterations in Protein Composition Beyond the ER Machinery.
Andreas Roos, Laxmikanth Kollipara, Stephan Buchkremer, Thomas Labisch, Eva Brauers

Mol Neurobiol· October 2016

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Proteome Profiling and Ultrastructural Characterization of the Human RCMH Cell Line: Myoblastic Properties and Suitability for Myopathological Studies.
Laxmikanth Kollipara, Stephan Buchkremer, Joachim Weis, Eva Brauers, Mareike Hoss

J Proteome Res· March 2016

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Myopathy in Marinesco-Sjögren syndrome links endoplasmic reticulum chaperone dysfunction to nuclear envelope pathology.
Andreas Roos, Stephan Buchkremer, Laxmikanth Kollipara, Thomas Labisch, Christian Gatz, Eva Brauers

Acta Neuropathol· May 2014

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Differential effects of myopathy-associated caveolin-3 mutants on growth factor signaling.
Eva Brauers, Agnes Dreier, Andreas Roos, Berthold Wormland, Joachim Weis

Am J Pathol· July 2010

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Identification of novel cystinuria mutations in pediatric patients.
Eva Brauers, Kamil Hozyasz, Bozena Golabek, Malgorzata Slowik, Christa Schmidt

J Pediatr Urol· December 2006

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Gene symbol: SLC7A9. Disease: Cystinuria. Accession #Hm0545.
Eva Brauers, Thomas Eggermann

Hum Genet· February 2006

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Gene symbol: SLC3A1. Disease: Cystinuria. Accession #Hm0546.
Eva Brauers, Thomas Eggermann

Hum Genet· February 2006

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Gene symbol: SLC3A1. Disease: Cystinuria. Accession #Hm0547.
Eva Brauers, Thomas Eggermann

Hum Genet· February 2006

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