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Epigenetic Mechanisms in Hirschsprung Disease.
Torroglosa A, Villalba-Benito L, Luzón-Toro B, Fernández RM, Antiñolo G, Borrego S. Torroglosa A, et al. Int J Mol Sci. 2019 Jun 26;20(13):3123. doi: 10.3390/ijms20133123. Int J Mol Sci. 2019. PMID: 31247956 Free PMC article. Review.
Epigenetics in ENS development and Hirschsprung disease.
Torroglosa A, Alves MM, Fernández RM, Antiñolo G, Hofstra RM, Borrego S. Torroglosa A, et al. Dev Biol. 2016 Sep 15;417(2):209-16. doi: 10.1016/j.ydbio.2016.06.017. Epub 2016 Jun 16. Dev Biol. 2016. PMID: 27321561 Free article. Review.
Comprehensive analysis of NRG1 common and rare variants in Hirschsprung patients.
Luzón-Toro B, Torroglosa A, Núñez-Torres R, Enguix-Riego MV, Fernández RM, de Agustín JC, Antiñolo G, Borrego S. Luzón-Toro B, et al. Among authors: torroglosa a. PLoS One. 2012;7(5):e36524. doi: 10.1371/journal.pone.0036524. Epub 2012 May 4. PLoS One. 2012. PMID: 22574178 Free PMC article.
Four new loci associations discovered by pathway-based and network analyses of the genome-wide variability profile of Hirschsprung's disease.
Fernández RM, Bleda M, Núñez-Torres R, Medina I, Luzón-Toro B, García-Alonso L, Torroglosa A, Marbà M, Enguix-Riego MV, Montaner D, Antiñolo G, Dopazo J, Borrego S. Fernández RM, et al. Among authors: torroglosa a. Orphanet J Rare Dis. 2012 Dec 28;7:103. doi: 10.1186/1750-1172-7-103. Orphanet J Rare Dis. 2012. PMID: 23270508 Free PMC article.
Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.
Luzón-Toro B, Gui H, Ruiz-Ferrer M, Sze-Man Tang C, Fernández RM, Sham PC, Torroglosa A, Kwong-Hang Tam P, Espino-Paisán L, Cherny SS, Bleda M, Enguix-Riego Mdel V, Dopazo J, Antiñolo G, García-Barceló MM, Borrego S. Luzón-Toro B, et al. Among authors: torroglosa a. Sci Rep. 2015 Nov 12;5:16473. doi: 10.1038/srep16473. Sci Rep. 2015. PMID: 26559152 Free PMC article.
22 results