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American Journal of Ophthalmology|April 30, 2003
A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindnessFelix Karl Jacobi, Christian P Hamel, Bernard Arnaud, et al.Neuron|September 8, 2001
Munc18-1 promotes large dense-core vesicle dockingT Voets, R F Toonen, E C Brian, et al.Journal of Molecular Medicine (Berlin, Germany)|March 26, 2004
Refinement of the DFNA4 locus to a 1.44 Mb region in 19q13.33C M Pusch, B Meyer, S Kupka, et al.British Journal of Pharmacology|July 24, 2010
Identification of sites responsible for the potentiating effect of niflumic acid on ClC-Ka kidney chloride channelsG Zifarelli, A Liantonio, A Gradogna, et al.Scientific Reports|May 28, 2025
Wastewater sequencing from a rural community enables identification of widespread adaptive mutations in a SARS-CoV-2 alpha variantMichael J Conway, Michael P Novay, Carson M Pusch, et al.Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|May 6, 2008
Lack of Tff3 peptide results in hearing impairment and accelerated presbyacusisMaria Lubka, Marcus Müller, Mirela Baus-Loncar, et al.International Journal of Molecular Medicine|February 15, 2001
Complete form of X-linked congenital stationary night blindness: refined mapping and evidence of genetic homogeneityC M Pusch, J Maurer, J Ramser, et al.The Journal of Biological Chemistry|June 18, 2020
Dipeptidyl peptidase 3 modulates the renin-angiotensin system in miceShalinee Jha, Ulrike Taschler, Oliver Domenig, et al.Human Molecular Genetics|May 7, 2009
Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cellPaulina Heidrych, Ulrike Zimmermann, Stephanie Kuhn, et al.Journal of Lipid Research|May 1, 2020
Metabolic regulation of the lysosomal cofactor bis(monoacylglycero)phosphate in miceGernot F Grabner, Nermeen Fawzy, Renate Schreiber, et al.Pageof 25