Publications by authors named "Britta Keyser"

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Burst-Like Transcription of Mutant and Wildtype -Alleles as Possible Origin of Cell-to-Cell Contractile Imbalance in Hypertrophic Cardiomyopathy.
Judith Montag, Kathrin Kowalski, Mirza Makul, Pia Ernstberger, Ante Radocaj, Britta Keyser

Front Physiol· April 2018

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Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathy.
Judith Montag, Mandy Syring, Julia Rose, Anna-Lena Weber, Pia Ernstberger, Britta Keyser

J Muscle Res Cell Motil· August 2017

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Mitral valve prolapse syndrome and MASS phenotype: Stability of aortic dilatation but progression of mitral valve prolapse.
Moritz Rippe, Julie De Backer, Kerstin Kutsche, Laura Muiño Mosquera, Helke Schüler, Britta Keyser

Int J Cardiol Heart Vasc· March 2016

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Overexpression of Gremlin-1 in patients with Loeys-Dietz syndrome: implications on pathophysiology and early disease detection.
Jasmin Wellbrock, Sara Sheikhzadeh, Leticia Oliveira-Ferrer, Hauke Stamm, Mathias Hillebrand, Britta Keyser

PLoS One· February 2016

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Clinical utility gene card for: Hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches.
Mine Arslan-Kirchner, Eloisa Arbustini, Catherine Boileau, Philippe Charron, Anne H Child, Britta Keyser

Eur J Hum Genet· January 2016

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Blood-based microRNA signatures differentiate various forms of cardiac hypertrophy.
Anselm A Derda, Sabrina Thum, Johan M Lorenzen, Udo Bavendiek, Joerg Heineke, Britta Keyser

Int J Cardiol· October 2015

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The main pulmonary artery in adults: a controlled multicenter study with assessment of echocardiographic reference values, and the frequency of dilatation and aneurysm in Marfan syndrome.
Sara Sheikhzadeh, Julie De Backer, Neda Rahimian Gorgan, Meike Rybczynski, Mathias Hillebrand, Britta Keyser

Orphanet J Rare Dis· December 2014

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Total serum transforming growth factor-β1 is elevated in the entire spectrum of genetic aortic syndromes.
Mathias Hillebrand, Nathalie Millot, Sara Sheikhzadeh, Meike Rybczynski, Sabine Gerth, Britta Keyser

Clin Cardiol· November 2014

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Observational cohort study of ventricular arrhythmia in adults with Marfan syndrome caused by FBN1 mutations.
Ali Aydin, Baran A Adsay, Sara Sheikhzadeh, Britta Keyser, Meike Rybczynski

PLoS One· September 2014

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FBN1 gene mutation characteristics and clinical features for the prediction of mitral valve disease progression.
Kristin Kühne, Britta Keyser, Eike F Groene, Sara Sheikhzadeh, Christian Detter

Int J Cardiol· September 2013

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High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissections.
Ushanthine Kathiravel, Britta Keyser, Sabine Hoffjan, Judith Kötting, Melanie Müller

Mol Cell Probes· April 2013

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A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?
Cengiz Yalcinkaya, Ozdem Erturk, Beyhan Tuysuz, Gozde Yesil, Jonathan I M L Verbeke, Britta Keyser

Neuropediatrics· June 2012

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TGFBR3 variation is not a common cause of Marfan-like syndrome and Loeys-Dietz-like syndrome.
Krishna K Singh, Joerg Schmidtke, Britta Keyser, Mine Arslan-Kirchner

J Negat Results Biomed· February 2012

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Herpes simplex virus immediate-early protein ICP0 is targeted by SIAH-1 for proteasomal degradation.
Claus-Henning Nagel, Nina Albrecht, Kristijana Milovic-Holm, Lakshmikanth Mariyanna, Britta Keyser

J Virol· August 2011

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Glutaric aciduria type 1 metabolites impair the succinate transport from astrocytic to neuronal cells.
Jessica Lamp, Britta Keyser, David M Koeller, Kurt Ullrich, Thomas Braulke

J Biol Chem· May 2011

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Disease-causing missense mutations affect enzymatic activity, stability and oligomerization of glutaryl-CoA dehydrogenase (GCDH).
Britta Keyser, Chris Mühlhausen, Achim Dickmanns, Ernst Christensen, Nicole Muschol

Hum Mol Genet· December 2008

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Transport and distribution of 3-hydroxyglutaric acid before and during induced encephalopathic crises in a mouse model of glutaric aciduria type 1.
Britta Keyser, Markus Glatzel, Franziska Stellmer, Bastian Kortmann, Zoltan Lukacs

Biochim Biophys Acta· June 2008

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3-Hydroxyglutaric acid is transported via the sodium-dependent dicarboxylate transporter NaDC3.
Franziska Stellmer, Britta Keyser, Birgitta C Burckhardt, Hermann Koepsell, Thomas Streichert

J Mol Med (Berl)· July 2007

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