يعرض 1 - 4 نتائج من 4 نتيجة بحث عن '"mitochondrial ATP synthase F0 sub-complex subunit C"', وقت الاستعلام: 0.37s تنقيح النتائج
  1. 1
    Academic Journal
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    Academic Journal

    المصدر: Ophthalmology and Visual Science Faculty Publications

    وصف الملف: application/pdf

    Relation: Supplementary material associated with this article can be found in the online version at doi: 10.1016/j.dib.2020.106076 . It is also available for download as the additional file listed at the end of this record. This article refers to: Zhong, Y., Mohan, K., Liu, J., Al-Attar, A., Lin, P., Flight, R. M., Sun, Q., Warmoes, M. O., Deshpande, R. R., Liu, H., Jung, K. S., Mitov, M. I., Lin, N., Butterfield, D. A., Lu, S., Liu, J., Moseley, H. N. B., Fan, T. W. M., Kleinman, M. E., & Wang, Q. J. (2020). Loss of CLN3 , the gene mutated in juvenile neuronal ceroid lipofuscinosis, leads to metabolic impairment and autophagy induction in retinal pigment epithelium. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease , 1866 (10), 165883. https://doi.org/10.1016/j.bbadis.2020.165883; https://uknowledge.uky.edu/ophthalmology_facpub/15; https://uknowledge.uky.edu/cgi/viewcontent.cgi?article=1014&context=ophthalmology_facpub

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    Dissertation/ Thesis