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Molecular Neurobiology|September 22, 2012
Spinocerebellar ataxia type 2: clinical presentation, molecular mechanisms, and therapeutic perspectivesJ J Magaña, L Velázquez-Pérez, B Cisneros
International Journal of Oral and Maxillofacial Surgery|February 20, 2026
SRY-box transcription factor 9 and insulin-like growth factor 1 as potential regulators in the pathogenesis of unilateral condylar hyperplasia: a pilot studyJ Chaurand, P Mondragón-Terán, J J Magaña-Quiñones, et al.
Molecular Biology Reports|July 17, 2010
Distribution of CTG repeats at the DMPK gene in myotonic dystrophy patients and healthy individuals from the Mexican populationJ J Magaña, P Cortés-Reynosa, R Escobar-Cedillo, et al.
Molecular Biology Reports|October 14, 2014
Altered nuclear structure in myotonic dystrophy type 1-derived fibroblastsR Rodríguez, O Hernández-Hernández, J J Magaña, et al.
Clinical Genetics|October 10, 2006
Association of the CT gene (CA) polymorphism with BMD in osteoporotic Mexican womenJ J Magaña, R Gómez, B Cisneros, et al.
Clinical Genetics|October 24, 2007
Association of the estrogen receptor alpha gene polymorphisms with osteoporosis in the Mexican populationR Gómez, J J Magaña, B Cisneros, et al.
Cerebellum (London, England)|July 6, 2013
Origin of the spinocerebellar ataxia type 7 gene mutation in Mexican populationJ J Magaña, R Gómez, M Maldonado-Rodríguez, et al.
The Knee|September 9, 2009
Association of the calcitonin gene (CA) polymorphism with osteoarthritis of the knee in a Mexican mestizo populationJ J Magaña, A Gálvez-Rosas, C González-Huerta, et al.
Genetics and Molecular Research : GMR|April 14, 2015
Interethnic variation of the MMP-9 microsatellite in Amerindian and Mexican Mestizo populations: considerations for genetic association studiesR Camacho-Mejorado, G Noris, C Santana, et al.
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