Drug discovery for spinal muscular atrophy
Author:
Publisher
Informa Healthcare
Subject
Drug Discovery
Link
http://www.tandfonline.com/doi/pdf/10.1517/17460441.2.4.437
Reference112 articles.
1. Identification and characterization of a spinal muscular atrophy-determining gene
2. Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy.
3. Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal Muscular Atrophy
4. International SMA Consortium Meeting (26–28 June 1992, Bonn, Germany)
5. Clinical Spectrum and Diagnostic Criteria of Infantile Spinal Muscular Atrophy: Further Delineation on the Basis of SMN Gene Deletion Findings
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1. The potential role of miRNA therapies in spinal muscle atrophy;Journal of the Neurological Sciences;2021-08
2. 2-Aminothiazoles;Privileged Structures in Drug Discovery;2018-03-09
3. Discovery, Synthesis, and Biological Evaluation of Novel SMN Protein Modulators;Journal of Medicinal Chemistry;2011-08-19
4. SAHA ameliorates the SMA phenotype in two mouse models for spinal muscular atrophy;Human Molecular Genetics;2010-01-22
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