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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: cisneros b. 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
Regulation of Ca v 3.1 channels by glucocorticoids.
Avila T, Hernández-Hernández O, Almanza A, de León MB, Urban M, Soto E, Cisneros B, Felix R. Avila T, et al. Among authors: cisneros b. Cell Mol Neurobiol. 2009 Dec;29(8):1265-73. doi: 10.1007/s10571-009-9422-2. Cell Mol Neurobiol. 2009. PMID: 19533336
[Pathogenesis of myotonic dystrophy type 1].
Magaña JJ, Leyva-García N, Cisneros B. Magaña JJ, et al. Among authors: cisneros b. Gac Med Mex. 2009 Jul-Aug;145(4):331-7. Gac Med Mex. 2009. PMID: 20073433 Review. Spanish.
145 results