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Markus Pfister, M.D.

Affiliations: 
Faculty of Medicine Eberhard Karls Universität Tübingen, Tübingen, Baden-Württemberg, Germany 
Area:
hearing
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"Markus Pfister"
Mean distance: 20.67 (cluster 29)
 
Cross-listing: CSD Tree

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Anthony W. Gummer grad student 1993-1995 Universität Tübingen

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Publications

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Budde BS, Aly MA, Mohamed MR, et al. (2020) Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss. Clinical Genetics
Neuhaus C, Eisenberger T, Decker C, et al. (2017) Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome. Molecular Genetics & Genomic Medicine. 5: 531-552
Hassan MA, Shah AA, Szmida E, et al. (2015) A TMC1 (transmembrane channel-like 1) mutation (p.S320R) in a Polish family with hearing impairment. Journal of Applied Genetics
Dettling J, Franz C, Zimmermann U, et al. (2014) Autonomous functions of murine thyroid hormone receptor TRα and TRβ in cochlear hair cells. Molecular and Cellular Endocrinology. 382: 26-37
Lubka-Pathak M, Shah AA, Gallozzi M, et al. (2011) Altered expression of securin (Pttg1) and serpina3n in the auditory system of hearing-impaired Tff3-deficient mice. Cellular and Molecular Life Sciences : Cmls. 68: 2739-49
Mohamed MR, Alesutan I, Föller M, et al. (2010) Functional analysis of a novel I71N mutation in the GJB2 gene among Southern Egyptians causing autosomal recessive hearing loss. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 26: 959-66
Xia A, Gao SS, Yuan T, et al. (2010) Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation. Disease Models & Mechanisms. 3: 209-23
Mallur PS, Weisstuch A, Pfister M, et al. (2010) Aquaporin-2 and -4: Single nucleotide polymorphisms in Ménire's disease patients Audiological Medicine. 8: 18-23
Zak M, Bress A, Pfister M, et al. (2010) ERGIC2, a new member of the OTOF interactome connected with the DFNB9 form of hearing impairment New Biotechnology. 27
Baur M, Fransen E, Tropitzsch A, et al. (2009) [Influence of exogenic factors on age-related hearing impairment]. Hno. 57: 1023-8
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