Rosales-Reynoso MA - Search Results

1

DNA repair/replication transcripts are down regulated in patients with Fragile X Syndrome.

Xu H, Rosales-Reynoso MA, Barros-Núñez P, Peprah E. Xu H, et al. BMC Res Notes. 2013 Mar 11;6:90. doi: 10.1186/1756-0500-6-90. BMC Res Notes. 2013. PMID: 23497562 Free PMC article.

2

[Usefulness of molecular biology techniques in the diagnosis of fragile X syndrome].

Rosales-Reynoso MA, Barros-Núñez P. Rosales-Reynoso MA, et al. Gac Med Mex. 2003 Jul-Aug;139(4):413-4. Gac Med Mex. 2003. PMID: 14574764 Spanish. No abstract available.

3

Genetic diversity at the FMR1 locus in Mexican population.

Rosales-Reynoso MA, Mendoza-Carrera F, Troyo-Sanromán R, Medina C, Barros-Núñez P. Rosales-Reynoso MA, et al. Arch Med Res. 2005 Jul-Aug;36(4):412-7. doi: 10.1016/j.arcmed.2004.05.005. Arch Med Res. 2005. PMID: 15950084

4

PCR approach for detection of Fragile X syndrome and Huntington disease based on modified DNA: limits and utility.

Rosales-Reynoso MA, Vilatela EA, Ojeda RM, Arce-Rivas A, Sandoval L, Troyo-Sanromán R, Barros-Núñez P. Rosales-Reynoso MA, et al. Genet Test. 2007 Summer;11(2):153-9. doi: 10.1089/gte.2006.0508. Genet Test. 2007. PMID: 17627386

5

Genetic variation of the FMR1 gene among four Mexican populations: Mestizo, Huichol, Purepecha, and Tarahumara.

Barros-Núñez P, Rosales-Reynoso MA, Sandoval L, Romero-Espinoza P, Troyo-Sanromán R, Ibarra B. Barros-Núñez P, et al. Am J Hum Biol. 2008 May-Jun;20(3):259-63. doi: 10.1002/ajhb.20705. Am J Hum Biol. 2008. PMID: 18172867

6

[Molecular diagnosis in Huntington's disease].

Rosales-Reynoso MA, Barros-Núñez P. Rosales-Reynoso MA, et al. Gac Med Mex. 2008 May-Jun;144(3):271-3. Gac Med Mex. 2008. PMID: 18714598 Spanish.

7

[Diseases caused by triplet expansion].

Rosales-Reynoso MA, Ochoa-Hernández AB, Barros-Núñez P. Rosales-Reynoso MA, et al. Rev Neurol. 2009 Jul 16-31;49(2):79-87. Rev Neurol. 2009. PMID: 19598137 Free article. Review. Spanish.

8

Gene expression profiling identifies WNT7A as a possible candidate gene for decreased cancer risk in fragile X syndrome patients.

Rosales-Reynoso MA, Ochoa-Hernández AB, Aguilar-Lemarroy A, Jave-Suárez LF, Troyo-Sanromán R, Barros-Núñez P. Rosales-Reynoso MA, et al. Arch Med Res. 2010 Feb;41(2):110-118.e2. doi: 10.1016/j.arcmed.2010.03.001. Arch Med Res. 2010. PMID: 20470940

9

FMR1 protein expression in blood smears for fragile X syndrome diagnosis in a Mexican population sample.

Romero-Espinoza P, Rosales-Reynoso MA, Willemsen R, Barros-Núñez P. Romero-Espinoza P, et al. Genet Test Mol Biomarkers. 2010 Aug;14(4):511-4. doi: 10.1089/gtmb.2009.0172. Genet Test Mol Biomarkers. 2010. PMID: 20642356

10

Peripheral T-lymphocytes express WNT7A and its restoration in leukemia-derived lymphoblasts inhibits cell proliferation.

Ochoa-Hernández AB, Ramos-Solano M, Meza-Canales ID, García-Castro B, Rosales-Reynoso MA, Rosales-Aviña JA, Barrera-Chairez E, Ortíz-Lazareno PC, Hernández-Flores G, Bravo-Cuellar A, Jave-Suarez LF, Barros-Núñez P, Aguilar-Lemarroy A. Ochoa-Hernández AB, et al. BMC Cancer. 2012 Feb 7;12:60. doi: 10.1186/1471-2407-12-60. BMC Cancer. 2012. PMID: 22313908 Free PMC article.

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