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Page 1
The Molecular Role of Polyamines in Age-Related Diseases: An Update.
Jimenez Gutierrez GE, Borbolla Jiménez FV, Muñoz LG, Tapia Guerrero YS, Murillo Melo NM, Cristóbal-Luna JM, Leyva Garcia N, Cordero-Martínez J, Magaña JJ. Jimenez Gutierrez GE, et al. Among authors: tapia guerrero ys. Int J Mol Sci. 2023 Nov 17;24(22):16469. doi: 10.3390/ijms242216469. Int J Mol Sci. 2023. PMID: 38003659 Free PMC article. Review.
Dp71 Point Mutations Induce Protein Aggregation, Loss of Nuclear Lamina Integrity and Impaired Braf35 and Ibraf Function in Neuronal Cells.
Rugerio-Martínez CI, Ramos D, Segura-Olvera A, Murillo-Melo NM, Tapia-Guerrero YS, Argüello-García R, Leyva-García N, Hernández-Hernández O, Cisneros B, Suárez-Sánchez R. Rugerio-Martínez CI, et al. Among authors: tapia guerrero ys. Int J Mol Sci. 2022 Oct 6;23(19):11876. doi: 10.3390/ijms231911876. Int J Mol Sci. 2022. PMID: 36233175 Free PMC article.
Wide Profiling of Circulating MicroRNAs in Spinocerebellar Ataxia Type 7.
Borgonio-Cuadra VM, Valdez-Vargas C, Romero-Córdoba S, Hidalgo-Miranda A, Tapia-Guerrero Y, Cerecedo-Zapata CM, Hernández-Hernández O, Cisneros B, Magaña JJ. Borgonio-Cuadra VM, et al. Mol Neurobiol. 2019 Sep;56(9):6106-6120. doi: 10.1007/s12035-019-1480-y. Epub 2019 Feb 5. Mol Neurobiol. 2019. PMID: 30721448
Coexistence of Fragile-X Syndrome, 8p23.1 Deletion, and Balanced Translocation t(7;10)(p10;q24) in a Single Family.
Cortés H, Reyes-Rosales M, Rojas-Velasco AJ, García-Juárez B, Tapia-Guerrero YS, Arenas-Diaz S, Leyva-García N, Macías-Gallardo JJ, Carrillo-Mora P, Magaña JJ. Cortés H, et al. Among authors: tapia guerrero ys. Genet Test Mol Biomarkers. 2020 Aug;24(8):527-531. doi: 10.1089/gtmb.2019.0276. Epub 2020 Jul 21. Genet Test Mol Biomarkers. 2020. PMID: 32716213
Genetic Distribution of Five Spinocerebellar Ataxia Microsatellite Loci in Mexican Native American Populations and Its Impact on Contemporary Mestizo Populations.
Gómez R, Tapia-Guerrero YS, Cisneros B, Orozco L, Cerecedo-Zapata C, Mendoza-Caamal E, Leyva-Gómez G, Leyva-García N, Velázquez-Pérez L, Magaña JJ. Gómez R, et al. Among authors: tapia guerrero ys. Genes (Basel). 2022 Jan 16;13(1):157. doi: 10.3390/genes13010157. Genes (Basel). 2022. PMID: 35052497 Free PMC article.
Clinical and molecular effect on offspring of a marriage of consanguineous spinocerebellar ataxia type 7 mutation carriers: a family case report.
Magaña JJ, Tapia-Guerrero YS, Velázquez-Pérez L, Cruz-Mariño T, Cerecedo-Zapata CM, Gómez R, Murillo-Melo NM, González-Piña R, Hernández-Hernández O, Cisneros B. Magaña JJ, et al. Among authors: tapia guerrero ys. Int J Clin Exp Med. 2014 Dec 15;7(12):5896-903. eCollection 2014. Int J Clin Exp Med. 2014. PMID: 25664129 Free PMC article.
Origin of the spinocerebellar ataxia type 7 gene mutation in Mexican population.
Magaña JJ, Gómez R, Maldonado-Rodríguez M, Velázquez-Pérez L, Tapia-Guerrero YS, Cortés H, Leyva-García N, Hernández-Hernández O, Cisneros B. Magaña JJ, et al. Among authors: tapia guerrero ys. Cerebellum. 2013 Dec;12(6):902-5. doi: 10.1007/s12311-013-0505-8. Cerebellum. 2013. PMID: 23828024
Analysis of CAG repeats in five SCA loci in Mexican population: epidemiological evidence of a SCA7 founder effect.
Magaña JJ, Tapia-Guerrero YS, Velázquez-Pérez L, Cerecedo-Zapata CM, Maldonado-Rodríguez M, Jano-Ito JS, Leyva-García N, González-Piña R, Martínez-Cruz E, Hernández-Hernández O, Cisneros B. Magaña JJ, et al. Among authors: tapia guerrero ys. Clin Genet. 2014 Feb;85(2):159-65. doi: 10.1111/cge.12114. Epub 2013 Mar 11. Clin Genet. 2014. PMID: 23368522
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