Found: 22
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Skeletal Muscle Pathogenesis in Polyglutamine Diseases.
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- Cells (2073-4409), 2022, v. 11, n. 13, p. N.PAG, doi. 10.3390/cells11132105
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- Article
Transplantation of clinical-grade human neural stem cells reduces neuroinflammation, prolongs survival and delays disease progression in the SOD1 rats.
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- Cell Death & Disease, 2019, v. 10, n. 5, p. N.PAG, doi. 10.1038/s41419-019-1582-5
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- Article
Establishment of stable iPS-derived human neural stem cell lines suitable for cell therapies.
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- Cell Death & Disease, 2018, v. 9, n. 10, p. 1, doi. 10.1038/s41419-018-0990-2
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- Article
Nitric oxide deficiency determines global chromatin changes in Duchenne muscular dystrophy.
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- FASEB Journal, 2009, v. 23, n. 7, p. 2131, doi. 10.1096/fj.08-115618
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- Article
Known Drugs Identified by Structure-Based Virtual Screening Are Able to Bind Sigma-1 Receptor and Increase Growth of Huntington Disease Patient-Derived Cells.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 3, p. 1293, doi. 10.3390/ijms22031293
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- Article
A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System—A Close Look at Chromosome 15.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 5, p. 1860, doi. 10.3390/ijms21051860
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- Article
A Multi-Layered Study on Harmonic Oscillations in Mammalian Genomics and Proteomics.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 18, p. 4585, doi. 10.3390/ijms20184585
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- Article
Parkin Mutation Affects Clock Gene-Dependent Energy Metabolism.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 11, p. 2772, doi. 10.3390/ijms20112772
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- Article
Reciprocal Interactions of Mitochondria and the Neuroimmunoendocrine System in Neurodegenerative Disorders: An Important Role for Melatonin Regulation.
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- Frontiers in Physiology, 2018, p. 1, doi. 10.3389/fphys.2018.00199
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- Article
Amniotic fluid stem cell‐derived extracellular vesicles educate type 2 conventional dendritic cells to rescue autoimmune disorders in a multiple sclerosis mouse model.
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- Journal of Extracellular Vesicles, 2024, v. 13, n. 6, p. 1, doi. 10.1002/jev2.12446
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- Article
Nitric Oxide Determines Mesodermic Differentiation of Mouse Embryonic Stem Cells by Activating Class lIa Histone Deacetylases: Potential Therapeutic Implications in a Mouse Model of Hindlimb Ischemia.
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- Stem Cells, 2010, v. 28, n. 3, p. 431, doi. 10.1002/stem.300
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- Article
DP71 and SERCA2 alteration in human neurons of a Duchenne muscular dystrophy patient.
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- Stem Cell Research & Therapy, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13287-018-1125-5
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- Article
Metabolic Profile of Patients with Smith-Magenis Syndrome: An Observational Study with Literature Review.
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- Children, 2023, v. 10, n. 9, p. 1451, doi. 10.3390/children10091451
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- Article
COVID-19 Specific Immune Markers Revealed by Single Cell Phenotypic Profiling.
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- Biomedicines, 2021, v. 9, n. 12, p. 1794, doi. 10.3390/biomedicines9121794
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- Article
NO points to epigenetics in vascular development.
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- Cardiovascular Research, 2011, v. 90, n. 3, p. 447, doi. 10.1093/cvr/cvr056
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- Article
The histone deacetylase inhibitor suberoylanilide hydroxamic acid reduces cardiac arrhythmias in dystrophic mice.
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- Cardiovascular Research, 2010, v. 87, n. 1, p. 73, doi. 10.1093/cvr/cvq035
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- Article
Stem cells from human amniotic fluid exert immunoregulatory function via secreted indoleamine 2,3-dioxygenase1.
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- Journal of Cellular & Molecular Medicine, 2015, v. 19, n. 7, p. 1593, doi. 10.1111/jcmm.12534
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- Article
Common atrium/atrioventricular canal defect and postaxial polydactyly: A mild clinical subtype of Ellis‐van Creveld syndrome caused by hypomorphic mutations in the EVC gene.
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- Human Mutation, 2020, v. 41, n. 12, p. 2087, doi. 10.1002/humu.24112
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- Article
Smith Magenis syndrome: First case of congenital heart defect in a patient with Rai1 mutation.
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- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 7, p. 2184, doi. 10.1002/ajmg.a.62740
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- Article
Glucose transportation in the brain and its impairment in Huntington disease: one more shade of the energetic metabolism failure?
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- Amino Acids, 2017, v. 49, n. 7, p. 1147, doi. 10.1007/s00726-017-2417-2
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- Article
Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients.
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- Antioxidants, 2022, v. 11, n. 5, p. 815, doi. 10.3390/antiox11050815
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- Article
Non coding RNA and brain.
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- BMC Neuroscience, 2006, v. 7, p. S5, doi. 10.1186/1471-2202-7-S1-S5
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- Article