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Drug Development for Target Ribosomal Protein rpL35/uL29 for Repair of LAMB3R635X in Rare Skin Disease Epidermolysis Bullosa.
- Published in:
- Skin Pharmacology & Physiology, 2021, v. 34, n. 4, p. 167, doi. 10.1159/000513260
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- Article
Localization and possible function of the glutamate transporter, EAAC1, in the rat retina.
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- Cell & Tissue Research, 2002, v. 310, n. 1, p. 31, doi. 10.1007/s00441-002-0612-1
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- Article
Stop codon readthrough as a treatment option for epidermolysis bullosa—Where we are and where we are going.
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- Experimental Dermatology, 2024, v. 33, n. 3, p. 1, doi. 10.1111/exd.15042
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- Article
Cloning, transport properties, and differential localization of two splice variants of GLT-1 in the rat CNS: Implications for CNS glutamate homeostasis.
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- Glia, 2004, v. 45, n. 2, p. 155, doi. 10.1002/glia.10317
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- Article
Emerging Personalized Opportunities for Enhancing Translational Readthrough in Rare Genetic Diseases and Beyond.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 7, p. 6101, doi. 10.3390/ijms24076101
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- Article