Tissue-specific Aberrations of Gene Expression in HPRT-deficient Mice: Functional Complexity in a Monogenic Disease?
Author:
Publisher
Elsevier BV
Subject
Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine
Reference49 articles.
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1. Lesch-Nyhan disease: I. Construction of expression vectors for hypoxanthine-guanine phosphoribosyltransferase (HGprt) enzyme and amyloid precursor protein (APP);Nucleosides, Nucleotides & Nucleic Acids;2020-04-20
2. Animal and cell models for Lesch-Nyhan syndrome;Drug Discovery Today: Disease Models;2020
3. Generation of hypoxanthine phosphoribosyltransferase gene knockout rabbits by homologous recombination and gene trapping through somatic cell nuclear transfer;Scientific Reports;2015-11-02
4. Alzheimer’s disease shares gene expression aberrations with purinergic dysregulation of HPRT deficiency (Lesch–Nyhan disease);Neuroscience Letters;2015-03
5. MicroRNAs;Advances in Genetics;2015
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