Blanz, Judith
Northwestern University
4 papers on CoChatORCID 0000-0002-0150-4732
Most cited papers
- Verified
Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficient mice
Tanaka, Y., Guhde, G., Suter, A., Eskelinen, E.-L., Hartmann, D., Lüllmann-Rauch, R., Janssen, P. M. L., Blanz, J., von Figura, K., & Saftig, P. (2000) · Nature
Autophagy in Disease and TherapyGlycogen Storage Diseases and Myoclonus
Cited by 925
- Verified
Dopamine oxidation mediates mitochondrial and lysosomal dysfunction in Parkinson’s disease
Burbulla, L. F., Song, P., Mazzulli, J. R., Zampese, E., Wong, Y. C., Jeon, S., Santos, D. P., Blanz, J., Obermaier, C. D., Strojny, C., et al. (2017) · Science
Parkinson's Disease Mechanisms and TreatmentsAutophagy in Disease and Therapy
Cited by 874
- Verified
Genetic LAMP2 deficiency accelerates the age-associated formation of basal laminar deposits in the retina
Notomi, S., Ishihara, K., Efstathiou, N. E., Lee, J.-J., Hisatomi, T., Tachibana, T., Konstantinou, E. K., Ueta, T., Murakami, Y., Maidana, D. E., et al. (2019) · Proceedings of the National Academy of Sciences
Retinal Diseases and TreatmentsAutophagy in Disease and Therapy
Cited by 92
- Verified
Peroxisomal dysfunctions cause lysosomal storage and axonal Kv1 channel redistribution in peripheral neuropathy
Kleinecke, S., Richert, S., de Hoz, L., Brügger, B., Kungl, T., Asadollahi, E., Quintes, S., Blanz, J., McGonigal, R., Naseri, K., et al. (2017) · eLife
Hereditary Neurological DisordersLysosomal Storage Disorders Research
Cited by 46
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