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Page 1
The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1.
Ballester-Lopez A, Linares-Pardo I, Koehorst E, Núñez-Manchón J, Pintos-Morell G, Coll-Cantí J, Almendrote M, Lucente G, Arbex A, Magaña JJ, Murillo-Melo NM, Lucia A, Monckton DG, Cumming SA, Ramos-Fransi A, Martínez-Piñeiro A, Nogales-Gadea G. Ballester-Lopez A, et al. Among authors: magana jj. Genes (Basel). 2020 Jul 7;11(7):757. doi: 10.3390/genes11070757. Genes (Basel). 2020. PMID: 32645888 Free PMC article.
Metabolic Reprogramming in SARS-CoV-2 Infection Impacts the Outcome of COVID-19 Patients.
Martínez-Gómez LE, Ibarra-González I, Fernández-Lainez C, Tusie T, Moreno-Macías H, Martinez-Armenta C, Jimenez-Gutierrez GE, Vázquez-Cárdenas P, Vidal-Vázquez P, Ramírez-Hinojosa JP, Rodríguez-Zulueta AP, Vargas-Alarcón G, Rojas-Velasco G, Sánchez-Muñoz F, Posadas-Sanchez R, Martínez-Ruiz FJ, Zayago-Angeles DM, Moreno ML, Barajas-Galicia E, Lopez-Cisneros G, Gonzalez-Fernández NC, Ortega-Peña S, Herrera-López B, Olea-Torres J, Juárez-Arias M, Rosas-Vásquez M, Cabrera-Nieto SA, Magaña JJ, Camacho-Rea MDC, Suarez-Ahedo C, Coronado-Zarco I, Valdespino-Vázquez MY, Martínez-Nava GA, Pineda C, Vela-Amieva M, López-Reyes A; Mex-Gen-COVID Initiative Group. Martínez-Gómez LE, et al. Among authors: magana jj. Front Immunol. 2022 Jul 11;13:936106. doi: 10.3389/fimmu.2022.936106. eCollection 2022. Front Immunol. 2022. PMID: 36341434 Free PMC article.
RNA Foci Formation in a Retinal Glial Model for Spinocerebellar Ataxia Type 7.
Suárez-Sánchez R, Ávila-Avilés RD, Hernández-Hernández JM, Sánchez-Celis D, Azotla-Vilchis CN, Gómez-Macías ER, Leyva-García N, Ortega A, Magaña JJ, Cisneros B, Hernández-Hernández O. Suárez-Sánchez R, et al. Among authors: magana jj. Life (Basel). 2022 Dec 22;13(1):23. doi: 10.3390/life13010023. Life (Basel). 2022. PMID: 36675972 Free PMC article.
Altered nuclear structure in myotonic dystrophy type 1-derived fibroblasts.
Rodríguez R, Hernández-Hernández O, Magaña JJ, González-Ramírez R, García-López ES, Cisneros B. Rodríguez R, et al. Among authors: magana jj. Mol Biol Rep. 2015 Feb;42(2):479-88. doi: 10.1007/s11033-014-3791-4. Epub 2014 Oct 12. Mol Biol Rep. 2015. PMID: 25307018
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. 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 myotonic dystrophy type 1 mutation in Mexican population and influence of Amerindian ancestry on CTG repeat allelic distribution.
Murillo-Melo NM, Márquez-Quiróz LC, Gómez R, Orozco L, Mendoza-Caamal E, Tapia-Guerrero YS, Camacho-Mejorado R, Cortés H, López-Reyes A, Santana C, Noris G, Hernández-Hernández O, Cisneros B, Magaña JJ. Murillo-Melo NM, et al. Among authors: magana jj. Neuromuscul Disord. 2017 Dec;27(12):1106-1114. doi: 10.1016/j.nmd.2017.09.004. Epub 2017 Sep 21. Neuromuscul Disord. 2017. PMID: 29054426
Oropharyngeal dysphagia in early stages of myotonic dystrophy type 1.
Franco-Guerrero AA, Márquez-Quiroz LC, Valadéz-Jiménez VM, Cortés H, Murillo-Melo NM, Muñoz B, Cisneros B, Magaña JJ. Franco-Guerrero AA, et al. Among authors: magana jj. Muscle Nerve. 2019 Jul;60(1):90-95. doi: 10.1002/mus.26485. Epub 2019 May 6. Muscle Nerve. 2019. PMID: 30994189
86 results