Publications by authors named "Sandra Passmann"

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Phosphorylation-dependent signaling controls degradation of DNA mismatch repair protein PMS2.
Inga Hinrichsen, Isabel M Weßbecher, Meik Huhn, Sandra Passmann, Stefan Zeuzem

Mol Carcinog· December 2017

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Origin, prevalence and response to therapy of hepatitis C virus genotype 2k/1b chimeras.
Simone Susser, Julia Dietz, Bernhard Schlevogt, Eli Zuckerman, Mira Barak, Sandra Passmann

J Hepatol· October 2017

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Promoter methylation of MLH1, PMS2, MSH2 and p16 is a phenomenon of advanced-stage HCCs.
Inga Hinrichsen, Matthias Kemp, Jan Peveling-Oberhag, Sandra Passmann, Guido Plotz

PLoS One· September 2014

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Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1.
Inga Hinrichsen, Benjamin Philipp Ernst, Franziska Nuber, Sandra Passmann, Dieter Schäfer

Mol Cancer· January 2014

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C-terminal fluorescent labeling impairs functionality of DNA mismatch repair proteins.
Angela Brieger, Guido Plotz, Inga Hinrichsen, Sandra Passmann, Ronja Adam

PLoS One· July 2012

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A CRM1-dependent nuclear export pathway is involved in the regulation of MutLα subcellular localization.
Angela Brieger, Ronja Adam, Sandra Passmann, Guido Plotz, Stefan Zeuzem

Genes Chromosomes Cancer· February 2011

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Cytoskeletal scaffolding proteins interact with Lynch-Syndrome associated mismatch repair protein MLH1.
Angela Brieger, Boris Adryan, Fabian Wolpert, Sandra Passmann, Stefan Zeuzem

Proteomics· September 2010

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An interstitial deletion at 3p21.3 results in the genetic fusion of MLH1 and ITGA9 in a Lynch syndrome family.
Claus Meyer, Angela Brieger, Guido Plotz, Nicole Weber, Sandra Passmann

Clin Cancer Res· February 2009

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