Focus on Molecules: Prominin-1 (CD133)
Author:
Publisher
Elsevier BV
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Reference4 articles.
1. Prominin: a story of cholesterol, plasma membrane protrusions and human pathology;Corbeil;Traffic,2001
2. Fargeas, C.A., Fonseca, A.-V., Huttner, W.B., Corbeil, D., 2006. Prominin-1 (CD133) – from progenitor cells to human diseases. Future Lipidology 1, 213–225 (review).
3. A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration;Maw;Hum. Mol. Genet.,2000
4. The genetics of inherited macular dystrophies;Michaelides;J. Med. Genet.,2003
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1. The Impact of Glycosylation on the Functional Activity of CD133 and the Accuracy of Its Immunodetection;Biology;2024-06-18
2. Emerging roles of prominin-1 (CD133) in the dynamics of plasma membrane architecture and cell signaling pathways in health and disease;Cellular & Molecular Biology Letters;2024-03-26
3. Identification of a cryptic functional apolipophorin-III domain within the Prominin-1 gene of Litopenaeus vannamei;Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology;2024-02
4. Can CD133 Be Regarded as a Prognostic Biomarker in Oncology: Pros and Cons;International Journal of Molecular Sciences;2023-12-12
5. Genetic and clinical characteristics of PROM1-related retinal degeneration in Korean;Scientific Reports;2023-12-11
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