Publications by authors named "Andreas BreSS"

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Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss.
Birgit S Budde, Maha Abdelgaber Aly, Mostafa R Mohamed, Andreas Breß, Janine Altmüller

Clin Genet· July 2020

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Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment.
Hazem Kaheel, Andreas Breß, Mohamed A Hassan, Aftab Ali Shah, Mutaz Amin

BMC Ear Nose Throat Disord· May 2018

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Frequency of c.35delG Mutation in Gene (Connexin 26) in Syrian Patients with Nonsyndromic Hearing Impairment.
Hazem Kaheel, Andreas Breß, Mohamed A Hassan, Aftab Ali Shah, Mutaz Amin

Genet Res Int· December 2017

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A TMC1 (transmembrane channel-like 1) mutation (p.S320R) in a Polish family with hearing impairment.
Mohamed Ahamed Hassan, Aftab Ali Shah, Elzbieta Szmida, Robert Smigiel, Maria M Sasiadek, Andreas Bress

J Appl Genet· August 2015

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Rare variants in BMP2 and BMP4 found in otosclerosis patients reduce Smad signaling.
Megan Ealy, Nicole C Meyer, Johnny Cruz Corchado, Isabelle Schrauwen, Andreas Bress

Otol Neurotol· March 2014

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Autonomous functions of murine thyroid hormone receptor TRα and TRβ in cochlear hair cells.
Juliane Dettling, Christoph Franz, Ulrike Zimmermann, Sze Chim Lee, Andreas Bress

Mol Cell Endocrinol· January 2014

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Generation of somatic electromechanical force by outer hair cells may be influenced by prestin-CASK interaction at the basal junction with the Deiter's cell.
Jelka Cimerman, Jörg Waldhaus, Csaba Harasztosi, Susanne V Duncker, Juliane Dettling, Andreas Bress

Histochem Cell Biol· August 2013

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Ergic2, a brain specific interacting partner of Otoferlin.
Magdalena Żak, Andreas Bress, Niels Brandt, Christoph Franz, Peter Ruth

Cell Physiol Biochem· November 2012

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Loss of mammal-specific tectorial membrane component carcinoembryonic antigen cell adhesion molecule 16 (CEACAM16) leads to hearing impairment at low and high frequencies.
Robert Kammerer, Lukas Rüttiger, Rainer Riesenberg, Constanze Schäuble, Rosemarie Krupar, Andreas Bress

J Biol Chem· June 2012

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Temporal expression pattern of Fkbp8 in rodent cochlea.
Magdalena Zak, Andreas Bress, Markus Pfister, Nikolaus Blin

Cell Physiol Biochem· April 2012

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Functional analysis of a novel I71N mutation in the GJB2 gene among Southern Egyptians causing autosomal recessive hearing loss.
Mostafa R Mohamed, Ioana Alesutan, Michael Föller, Mentor Sopjani, Andreas Bress

Cell Physiol Biochem· April 2011

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Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation.
Anping Xia, Simon S Gao, Tao Yuan, Alexander Osborn, Andreas Bress

Dis Model Mech· May 2010

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Deafness in TRbeta mutants is caused by malformation of the tectorial membrane.
Harald Winter, Lukas Rüttiger, Marcus Müller, Stephanie Kuhn, Niels Brandt, Andreas Bress

J Neurosci· February 2009

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Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness form.
Paulina Heidrych, Ulrike Zimmermann, Andreas Bress, Carsten M Pusch, Peter Ruth

Hum Mol Genet· December 2008

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