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Dp71 Point Mutations Induce Protein Aggregation, Loss of Nuclear Lamina Integrity and Impaired Braf35 and Ibraf Function in Neuronal Cells.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 19, p. 11876, doi. 10.3390/ijms231911876
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- Article
Effects of Physical Rehabilitation in Patients with Spinocerebellar Ataxia Type 7.
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- Cerebellum, 2019, v. 18, n. 3, p. 397, doi. 10.1007/s12311-019-1006-1
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- Article
RNA Foci Formation in a Retinal Glial Model for Spinocerebellar Ataxia Type 7.
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- Life (2075-1729), 2023, v. 13, n. 1, p. 23, doi. 10.3390/life13010023
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- Article
Non-invasive methods for evaluation of skin manifestations in patients with ichthyosis.
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- Archives of Dermatological Research, 2020, v. 312, n. 4, p. 231, doi. 10.1007/s00403-019-01987-w
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- Article
Transcriptome Analysis Reveals Altered Inflammatory Pathway in an Inducible Glial Cell Model of Myotonic Dystrophy Type 1.
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- Biomolecules (2218-273X), 2021, v. 11, n. 2, p. 159, doi. 10.3390/biom11020159
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- Article
Severity of Dyskinesia and D3R Signaling Changes Induced by L-DOPA Treatment of Hemiparkinsonian Rats Are Features Inherent to the Treated Subjects.
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- Biomolecules (2218-273X), 2019, v. 9, n. 9, p. 431, doi. 10.3390/biom9090431
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- Article
High prevalence of autosomal recessive congenital ichthyosis in a Mexican population caused by a new mutation in the TGM1 gene: epidemiological evidence of a founder effect.
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- International Journal of Dermatology, 2020, v. 59, n. 8, p. 969, doi. 10.1111/ijd.14952
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- Article
Genetic Distribution of Five Spinocerebellar Ataxia Microsatellite Loci in Mexican Native American Populations and Its Impact on Contemporary Mestizo Populations.
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- Genes, 2022, v. 13, n. 1, p. 157, doi. 10.3390/genes13010157
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- Article
Current Overview of Spinocerebellar Ataxia Type 7 in Mexican Population: Challenges in Specialized Care for a Rare Disease.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 19, p. 10750, doi. 10.3390/ijms251910750
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- Article