Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss von Budde, Birgit S., Aly, Maha Abdelgaber, Mohamed, Mostafa R., Breß, Andreas, Altmüller, Janine, Motameny, Susanne, Kawalia, Amit, Thiele, Holger, Konrad, Kathryn, Becker, Christian, Toliat, Mohammad R., Nürnberg, Gudrun, Sayed, Eman Abdel Fattah, Mohamed, Enass Sayed, Pfister, Markus, Nürnberg, Peter

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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 von Kammerer, Robert, Rüttiger, Lukas, Riesenberg, Rainer, Schäuble, Constanze, Krupar, Rosemarie, Kamp, Annegret, Sunami, Kishiko, Eisenried, Andreas, Hennenberg, Martin, Grunert, Fritz, Bress, Andreas, Battaglia, Sebastiano, Schrewe, Heinrich, Knipper, Marlies, Schneider, Marlon R., Zimmermann, Wolfgang

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Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness form von Heidrych, Paulina, Zimmermann, Ulrike, Breß, Andreas, Pusch, Carsten M., Ruth, Peter, Pfister, Markus, Knipper, Marlies, Blin, Nikolaus

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

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Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation von Xia, Anping, Gao, Simon S, Yuan, Tao, Osborn, Alexander, Bress, Andreas, Pfister, Markus, Maricich, Stephen M, Pereira, Fred A, Oghalai, John S

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Ergic2, a Brain Specific Interacting Partner of Otoferlin von Zak, Magdalena, Breß, Andreas, Brandt, Niels, Franz, Christoph, Ruth, Peter, Pfister, Markus, Knipper, Marlies, Blin, Nikolaus

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Frequency of c.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients with Nonsyndromic Hearing Impairment von Kaheel, Hazem, Breß, Andreas, Hassan, Mohamed A., Shah, Aftab Ali, Amin, Mutaz, Bakhit, Yousuf H. Y., Kniper, Marlies

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113. Reliability of Nasopharyngeal PCR for the Detection of Otopathogens in Children with Uncomplicated Acute Otitis Media von Frost, Holly M, Sebastian, Thresia, Keith, Amy, Kurtz, Melanie, Bress, Andreas, Egan, Richard, Dominguez, Samuel R, Parker, Sarah, Jenkins, Timothy C

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Autonomous functions of murine thyroid hormone receptor TRα and TRβ in cochlear hair cells von Dettling, Juliane, Franz, Christoph, Zimmermann, Ulrike, Lee, Sze Chim, Bress, Andreas, Brandt, Niels, Feil, Robert, Pfister, Markus, Engel, Jutta, Flamant, Frédéric, Rüttiger, Lukas, Knipper, Marlies

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Temporal Expression Pattern of Fkbp8 in Rodent Cochlea von Zak, Magdalena, Bress, Andreas, Pfister, Markus, Blin, Nikolaus

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Rare Variants in BMP2 and BMP4 Found in Otosclerosis Patients Reduce Smad Signaling von Ealy, Megan, Meyer, Nicole C, Corchado, Johnny Cruz, Schrauwen, Isabelle, Bress, Andreas, Pfister, Markus, Van Camp, Guy, Smith, Richard J H

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

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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 von Cimerman, Jelka, Waldhaus, Jörg, Harasztosi, Csaba, Duncker, Susanne V., Dettling, Juliane, Heidrych, Paulina, Bress, Andreas, Gampe-Braig, Claudia, Frank, Gerhard, Gummer, Anthony W., Oliver, Dominik, Knipper, Marlies, Zimmermann, Ulrike

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Deafness in TRβ Mutants Is Caused by Malformation of the Tectorial Membrane von Winter, Harald, Rüttiger, Lukas, Müller, Marcus, Kuhn, Stephanie, Brandt, Niels, Zimmermann, Ulrike, Hirt, Bernhard, Bress, Andreas, Sausbier, Matthias, Conscience, Aude, Flamant, Frederic, Tian, Yong, Zuo, Jian, Pfister, Markus, Ruth, Peter, Löwenheim, Hubert, Samarut, Jacques, Engel, Jutta, Knipper, Marlies

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Functional Analysis of a Novel I71N Mutation in the GJB2 Gene Among Southern Egyptians Causing Autosomal Recessive Hearing Loss von Mohamed, Mostafa R., Alesutan, Ioana, FÖller, Michael, Sopjani, Mentor, Bress, Andreas, Baur, Manuela, Salama, Ragaa H.M., Bakr, Mohamed S., Mohamed, Mohamed A., Blin, Nikolaus, Lang, Florian, Pfister, Markus

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Deafness in TRbeta mutants is caused by malformation of the tectorial membrane von Winter, Harald, Rüttiger, Lukas, Müller, Marcus, Kuhn, Stephanie, Brandt, Niels, Zimmermann, Ulrike, Hirt, Bernhard, Bress, Andreas, Sausbier, Matthias, Conscience, Aude, Flamant, Frederic, Tian, Yong, Zuo, Jian, Pfister, Markus, Ruth, Peter, Löwenheim, Hubert, Samarut, Jacques, Engel, Jutta, Knipper, Marlies

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Deafness in TR{beta} Mutants Is Caused by Malformation of the Tectorial Membrane von Winter, Harald, Ruttiger, Lukas, Muller, Marcus, Kuhn, Stephanie, Brandt, Niels, Zimmermann, Ulrike, Hirt, Bernhard, Bress, Andreas, Sausbier, Matthias, Conscience, Aude, Flamant, Frederic, Tian, Yong, Zuo, Jian, Pfister, Markus, Ruth, Peter, Lowenheim, Hubert, Samarut, Jacques, Engel, Jutta, Knipper, Marlies

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An intermediate representation for optimizing machine learning pipelines von Kunft, Andreas, Katsifodimos, Asterios, Schelter, Sebastian, Breß, Sebastian, Rabl, Tilmann, Markl, Volker

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Toward GPU-accelerated Database Optimization von Meister, Andreas, Breß, Sebastian, Saake, Gunter

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Digitalisierung: Begriff, Ziele und Steuerung von Heuermann, Roland, Engel, Andreas, von Lucke, Jörn

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