Hübner, Christian A.

Regulation of endoplasmic reticulum turnover by selective autophagy

Khaminets, A., Heinrich, T., Mari, M., Grumati, P., Huebner, A. K., Akutsu, M., Liebmann, L., Stolz, A., Nietzsche, S., Koch, N., et al. (2015) · Nature

Autophagy in Disease and TherapyEndoplasmic Reticulum Stress and Disease

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Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy

Kurth, I., Pamminger, T., Hennings, J. C., Soehendra, D., Huebner, A. K., Rotthier, A., Baets, J., Senderek, J., Topaloglu, H., Farrell, S. A., et al. (2009) · Nature Genetics

Hereditary Neurological DisordersPain Mechanisms and Treatments

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Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy

Janecke, A. R., Thompson, D. A., Utermann, G., Becker, C., Hübner, C. A., Schmid, E., McHenry, C. L., Nair, A. R., Rüschendorf, F., Heckenlively, J., et al. (2004) · Nature Genetics

Retinal Development and DisordersRetinal Diseases and Treatments

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Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3

Kornak, U., Mademan, I., Schinke, M., Voigt, M., Krawitz, P., Hecht, J., Barvencik, F., Schinke, T., Gießelmann, S., Beil, F. T., et al. (2014) · Brain

Hereditary Neurological DisordersCellular transport and secretion

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Rdh12 activity and effects on retinoid processing in the murine retina

Chrispell, J. D., Feathers, K. L., Kane, M. A., Kim, C. Y., Brooks, M., Khanna, R., Kurth, I., Hübner, C. A., Gal, A., Mears, A. J., et al. (2009) · Journal of Biological Chemistry

Retinal Development and DisordersRetinoids in leukemia and cellular processes

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Molecular and functional characterization of Kv4.2 and KChIP2 expressed in the porcine left ventricle

Schultz, J.-H., Volk, T., Bassalaý, P., Hennings, J. C., Hübner, C. A., & Ehmke, H. (2007) · Pflügers Archiv - European Journal of Physiology

Ion channel regulation and functionCardiac electrophysiology and arrhythmias

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