Sociedad Mexicana de Epigenética y Medicina Regenerativa A.C. 

2017

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The myogenic regulatory factors, determinants of muscle development, cell identity and regeneration. Hernández-Hernández JM, García-González EG, Brun CE, Rudnicki MA. Semin Cell Dev Biol. 2017 Dec;72:10-18. doi: 10.1016/j.semcdb.2017.11.010. Epub 2017 Nov 15.

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Harnessing BET Inhibitor Sensitivity Reveals AMIGO2 as a Melanoma Survival Gene. Fontanals-Cirera B, Hasson D,  ardabasso C, Di Micco R, Agrawal P, Chowdhury A, Gantz M, de Pablos-Aragoneses A, Morgenstern A, Wu P, Filipescu D, Valle-Garcia D, Darvishian F, Roe JS, Davies MA, Vakoc CR, Hernando E, Bernstein E. Mol Cell. 2017 Nov 16;68(4):731-744.e9. doi: 10.1016/j.molcel.2017.11.004

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ATRX and DAXX: Mechanisms and Mutations. Dyer MA, Qadeer ZA, Valle-Garcia D, Bernstein E. Cold Spring Harb Perspect Med. 2017 Mar 1;7(3). pii: a026567. doi: 10.1101/cshperspect.a026567. Review. 

 

MicroRNAs driving invasion and metastasis in ovarian cancer: Opportunities for translational medicine (Review).  Palma Flores C, García-Vázquez R, Gallardo Rincón D, Ruiz-García E, Astudillo de la Vega H, Marchat LA, Salinas Vera YM, López-Camarillo C.  Int J Oncol. 2017 May;50(5):1461-1476. doi: 10.3892/ijo.2017.3948. Epub 2017

Apr 4

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A Complete Association of an intronic SNP rs6798742 with Origin of Spinocerebellar Ataxia Type 7-CAG Expansion Loci in the Indian and Mexican Population. Faruq M, Magaña JJ, Suroliya V, Narang A, Murillo-Melo NM, Hernández-Hernández O, Srivastava AK, Mukerji M. Ann Hum Genet. 2017 Sep;81(5):197-204. doi: 10.1111/ahg.12200. Epub 2017 Jun 9.

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Voice Alterations in Patients With Spinocerebellar Ataxia Type 7 (SCA7): Clinical-Genetic Correlations. Gómez-Coello A, Valadez-Jiménez VM, Cisneros B, Carrillo-Mora P, Parra-Cárdenas M, Hernández-Hernández O, Magaña JJ. J Voice. 2017 Jan;31(1):123.e1-123.e5. doi: 10.1016/j.jvoice.2016.01.010. Epub 2016 Mar 15.

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(-)-Epicatechin induces physiological cardiac growth by activation of the PI3K/Akt pathway in mice. De Los Santos S, García-Pérez V, Hernández-Reséndiz S, Palma-Flores C, González-Gutiérrez CJ, Zazueta C, Canto P, Coral-Vázquez RM.

Mol Nutr Food Res. 2017 Feb;61(2). doi: 10.1002/mnfr.201600343. Epub 2016 Oct 10.

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Ataxia Type 7 (SCA7): Clinical-Genetic Correlations. Journal of voice : official journal of the Voice Foundation. Gómez-Coello A, Valadez-Jiménez VM, Cisneros B, Carrillo-Mora P, Parra-CárdenasM, Hernández-Hernández O, Magaña JJ. Voice Alterations in Patients WithSpinocerebellar 2017; 31(1):123.e1-123.e5.

 

2016

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Dysferlin quantification in monocytes for rapid screening fordysferlinopathies. Sánchez-Chapul L, Ángel-Muñoz MD, Ruano-Calderón L, Luna-Angulo A, Coral-Vázquez R, Hernández-Hernández Ó, Magaña JJ, León-Hernández SR, Escobar-Cedillo RE,Vargas S. Muscle & Nerve. 2016; 54(6):1064-1071.

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Dual targeting of ANGPT1 and TGFBR2 genes by miR-204 controls angiogenesis in breast cancer. -Pérez A, Marchat LA, Rodríguez-Cuevas S, Bautista-Piña V,Hidalgo-Miranda A, Ocampo EA, Martínez MS, Palma-Flores C, Fonseca-Sánchez MA, Astudillo-de la Vega H, Ruíz-García E, González-Barrios JA, Pérez-Plasencia C, Streber ML, López-Camarillo C. Sci Rep. 2016 Oct 5;6:34504. doi:10.1038/srep34504.

 

Chromatin remodeling effects on enhancer activity. García-González E, Escamilla-Del-Arenal M, Arzate-Mejía R, Recillas-Targa F. Cell Mol Life Sci. 2016 Aug;73(15):2897-910. doi: 10.1007/s00018-016-2184-3. 

 

(-)-Epicatechin induces physiological cardiac growth by activation of the pi3k/akt pathway inmice. De Los Santos S, García-Pérez V, Hernández-Reséndiz S, Palma-Flores C, González-Gutiérrez CJ, Zazueta C, Canto P, Coral-Vázquez RM. Mol Nutr Food Res. 2016 Sep 8. doi: 10.1002/mnfr.201600343.

 

The rs3857059 variant of the SNCA gene is associated with Parkinson's disease in MexicanMestizos.

García S, Chavira-Hernández G, Gallegos-Arreola MP, Dávila-Maldonado L, García Martínez F, Montes Almanza LA, Palma-Flores C, Mondragón-Terán P, Alcaraz Estrada SL, López-Hernández LB.

Arq Neuropsiquiatr. 2016 Jun;74(6):445-9. doi: 10.1590/0004-282X20160061.

 

ATRX binds to atypical chromatin domains at the 3' exons of zinc finger genes to preserve H3K9me3 enrichment. Valle-García D, Qadeer ZA, McHugh DS, Ghiraldini FG, Chowdhury AH, Hasson D, Dyer MA, Recillas-Targa F, Bernstein E. Epigenetics. 2016 Jun 2;11(6):398-414. doi: 10.1080/15592294.2016.1169351.

 

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2015

 

Functional Polymorphism rs13306560 of the MTHFR Gene Is Associated With Essential Hypertension in a Mexican-Mestizo Population. Pérez-Razo JC, Cano-Martínez LJ, Vargas Alarcón G, Canizales-Quinteros S, Martínez-Rodríguez N, Canto P, Roque-Ramírez B, Palma-Flores C, Esteban-Martínez R, López-Hernández LB, Rojano-Mejía D, Coral Vázquez RM. Circ Cardiovasc Genet. 2015 Aug;8(4):603-9. doi: 10.1161/CIRCGENETICS.114.000942.

 

Comparison of mutation profiles in the Duchenne muscular dystrophy gene among populations: implications for potential molecular therapies. López-Hernández LB, Gómez-Díaz B, Luna-Angulo AB, Anaya-Segura M, Bunyan DJ, Zúñiga-Guzman C, Escobar Cedillo RE, Roque-Ramírez B, Ruano-Calderón LA, Rangel-Villalobos H, López Hernández JA, Estrada-Mena FJ, García S, Coral-Vázquez RM. Int J Mol Sci. 2015 Mar 9;16(3):5334-46. doi: 10.3390/ijms16035334.

 

Contrasting roles for MyoD in organizing myogenic promoter structures during embryonic skeletal muscle development. Cho OH, Mallappa C, Hernández-Hernández JM, Rivera-Pérez JA, Imbalzano AN. Dev Dyn. 2015 Jan;244(1):43-55. doi: 10.1002/dvdy.24217.

 

Association of the rs1801133 variant in the MTHFR gene and sporadic Parkinson's disease.García S, Coral-Vázquez R, Gallegos-Arreola MP, Montes-Almanza LA, Canto P, García-Martínez FA, Chavira-Hernández G, Palma-Flores C, Dávila-Maldonado L, Cuevas-García CF, López Hernández LB.

Folia Neuropathol. 2015;53(1):24-8.

 

Reduction of no-reflow and reperfusion injury with the synthetic 17β-aminoestrogen compoundProlame is associated with PI3K/Akt/eNOS signaling cascade. Hernández-Reséndiz S, Palma-Flores C, De Los Santos S, Román-Anguiano NG, Flores M, de la Peña A, Flores PL, Fernández-G JM, Coral-Vázquez RM, Zazueta C. Basic Res Cardiol. 2015 Mar;110(2):1. doi: 10.1007/s00395-015-0464-y. 

 

Histone Variant H2A.Z.2 Mediates Proliferation and Drug Sensitivity of Malignant Melanoma. Vardabasso C, Gaspar-Maia A, Hasson D, Pünzeler S, Valle-Garcia D, Straub T, Keilhauer EC, Strub T, Dong J, Panda T, Chung CY, Yao JL, Singh R, Segura MF, Fontanals-Cirera B, Verma A, Mann M, Hernando E, Hake SB, Bernstein E. Mol Cell. 2015 Jul 2;59(1):75-88. doi: 10.1016/j.molcel.2015.05.009.

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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. A Molecular Biology Reports. 2015; 42(2):479-88.

 

Spinocerebellar ataxia type 7: a neurodegenerative disorder with peripheral neuropathy. Salas-Vargas J, Mancera-Gervacio J, Velázquez-Pérez L, Rodrígez-Labrada R, Martínez-Cruz E, Magaña JJ, Durand-Rivera A, Hernández-Hernández O, Cisneros B, Gonzalez-Piña R. European Neurology. 2015; 73(3-4):173-8.

 

Comprehensive clinical and genetic study of a large Mexican population with spinocerebellar ataxia type 7.  Velázquez-Pérez L, Cerecedo-Zapata CM, Hernández-Hernández O, Martínez-Cruz E, Tapia-Guerrero YS, González-Piña R, Salas-Vargas J, Rodríguez-Labrada R, Gurrola-Betancourth R, Leyva-García N, Cisneros B, Magaña JJ. A Neurogenetics. 2015; 16(1):11-21.

 

 

2014

 

A regulatory element affects the activity and chromatin structure of the chicken α-globin 3' enhancer. García-González E, Recillas-Targa F. Biochim Biophys Acta. 2014 Nov;1839(11):1233-41. doi: 10.1016/j.bbagrm.2014.09.009.

 

Expression pattern of mRNA A and mRNA B of alpha sarcoglycan gene during mouse embryonic development and regulation of their expression by myogenic and cardiogenic transcription factors. Roque-Ramírez B, Chimal-Monroy J, Canto P, Coral-Vázquez RM. Dev Dyn. 2014 Nov;243(11):1416-28. doi: 10.1002/dvdy.24175. Epub 2014 Aug 25.

 

(-)-Epicatechin improves mitochondrial-related protein levels and ameliorates oxidative stress in dystrophic δ-sarcoglycan null mouse striated muscle. Ramirez-Sanchez I, De los Santos S, Gonzalez-Basurto S, Canto P, Mendoza-Lorenzo P, Palma-Flores C, Ceballos-Reyes G, Villarreal F, Zentella-Dehesa A, Coral-Vazquez R. FEBS J. 2014 Dec;281(24):5567-80. doi: 10.1111/febs.13098. 

 

Description of a utrophin associated protein complex in lipid raft domains of human artery smooth muscle cells. Palma-Flores C, Ramírez-Sánchez I, Rosas-Vargas H, Canto P, Coral-Vázquez RM. Biochim Biophys Acta. 2014 Mar;1838(3):1047-54. doi: 10.1016/j.bbamem.2013.09.010. 

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Decreased expression of the chromatin remodeler ATRX associates with melanoma progression. Qadeer ZA, Harcharik S, Valle-Garcia D, Chen C, Birge MB, Vardabasso C, Duarte LF, Bernstein E. J Invest Dermatol. 2014 Jun;134(6):1768-72. doi: 10.1038/jid.2014.45.

 

The ATRX cDNA is prone to bacterial IS10 element insertions that alter its structure. Valle-García D, Griffiths LM, Dyer MA, Bernstein E, Recillas-Targa F. Springerplus. 2014 May 2;3:222. doi: 10.1186/2193-1801-3-222.

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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. International Journal of Clinical and Experimental Medicine. 2014; 7(12):5896-903.

 

Detection of the PMP22 gene duplication in peripheral neuropathy patients: a study in Mexican population. Cortés H, Hernández-Hernández Ó, Bautista-Tirado T, Escobar-Cedillo RE, Magaña JJ, Leyva-García N. . Revista de Neurologia. 2014; 59(3):111-7.

 

Nucleocytoplasmic shuttling of the Duchenne muscular dystrophy gene product dystrophin Dp71d is dependent on the importin α/β and CRM1 nuclear transporters and microtubule motor dynein. Suárez-Sánchez R, Aguilar A, Wagstaff KM, Velez G, Azuara-Medina PM, Gomez P, Vásquez-Limeta A, Hernández-Hernández O, Lieu KG, Jans DA, Cisneros B. Biochimica et Biophysica Acta. 2014;1843(5):985-1001.

 

Recessive spinocerebellar ataxia with paroxysmal cough attacks: a report of five cases. Velázquez-Pérez L, González-Piña R, Rodríguez-Labrada R, Aguilera-Rodríguez R, Galicia-Polo L, Vázquez-Mojena Y, Cortés-Rubio AM, Trujillo-Bracamontes MR, Cerecedo-Zapata CM, Hernández-Hernández O, Cisneros B, Magaña JJ.  Cerebellum (London, England). 2014; 13(2):215-21.

 

Analysis of CAG repeats in five SCA loci in Mexican population: epidemiological evidence of a SCA7 founder effect.

Magaña JJ, Tapia-Guerrero YS, Velázquez-Pérez L, Cerecedo-Zapata CM, Maldonado-Rodríguez M, Jano-Ito JS, Leyva-García N, González-Piña R, Martínez-Cruz E, Hernández-Hernández O, Cisneros B.  Clinical Genetics. 2014; 85(2):159-65.

 

 

2013

 

The Scaffold attachment factor b1 (Safb1) regulates myogenic differentiation by facilitating the transition of myogenic gene chromatin from a repressed to an activated state. Hernández-Hernández JM, Mallappa C, Nasipak BT, Oesterreich S, Imbalzano AN. Nucleic Acids Res. 2013 Jun;41(11):5704-16. doi: 10.1093/nar/gkt285. 

 

Wnt3 function in the epiblast is required for the maintenance but not the initiation of gastrulation in mice. Tortelote GG, Hernández-Hernández JM, Quaresma AJ, Nickerson JA, Imbalzano AN, Rivera-Pérez JA. Dev Biol. 2013 Feb 1;374(1):164-73. doi: 10.1016/j.ydbio.2012.10.013.

 

MacroH2A histone variants act as a barrier upon reprogramming towards pluripotency. Gaspar-Maia A, Qadeer ZA, Hasson D, Ratnakumar K, Leu NA, Leroy G, Liu S, Costanzi C, Valle-Garcia D, Schaniel C, Lemischka I, Garcia B, Pehrson JR, Bernstein E. Nat Commun. 2013;4:1565. doi: 10.1038/ncomms2582.

 

Origin of the spinocerebellar ataxia type 7 gene mutation in Mexican population. Magaña JJ, Gómez R, Maldonado-Rodríguez M, Velázquez-Pérez L, Tapia-Guerrero YS, Cortés H, Leyva-García N, Hernández-Hernández O, Cisneros B.Cerebellum (London, England). 2013; 12(6):902-5.

 

Synaptic protein dysregulation in myotonic dystrophy type 1: Disease neuropathogenesis beyond missplicing. Hernández-Hernández O, Sicot G, Dinca DM, Huguet A, Nicole A, Buée L, Munnich A, Sergeant N, Gourdon G, Gomes-Pereira M. S Rare Diseases (Austin, Tex.). 2013; 1:e25553.

 

Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour. Hernández-Hernández O, Guiraud-Dogan C, Sicot G, Huguet A, Luilier S, Steidl E, Saenger S, Marciniak E, Obriot H, Chevarin C, Nicole A, Revillod L, Charizanis K, Lee KY, Suzuki Y, Kimura T, Matsuura T, Cisneros B, Swanson MS, Trovero F, Buisson B, Bizot JC, Hamon M, Humez S, Bassez G, Metzger F, Buée L, Munnich A, Sergeant N, Gourdon G, Gomes-Pereira M. Brain : a Journal of Neurology. 2013; 136(Pt 3):957-70.

 

2012

 

Chronological and morphological study of heart development in the rat.

Marcela SG, Cristina RM, Angel PG, Manuel AM, Sofía DC, Patricia de LR, Bladimir RR, Concepción SG. Anat Rec (Hoboken). 2012 Aug;295(8):1267-90. doi: 10.1002/ar.22508. Epub 2012 Jun 19.

 

Immunodetection analysis of muscular dystrophies in Mexico. Gómez-Díaz B, Rosas-Vargas H, Roque-Ramírez B, Meza-Espinoza P, Ruano-Calderón LA, Fernández Valverde F, Escalante-Bautista D, Escobar-Cedillo RE, Sánchez-Chapul L, Vargas-Cañas S, López-Hernández LB, Bahena-Martínez E, Luna-Angulo AB, Canto P, Coral-Vázquez RM. Muscle Nerve. 2012 Mar;45(3):338-45. doi: 10.1002/mus.22314.

 

Caveolae and non-caveolae lipid raft microdomains of human umbilical vein endothelial cells contain utrophin-associated protein complexes. Ramírez-Sánchez I, Mendoza-Lorenzo P, Zentella-Dehesa A, Méndez-Bolaina E, Lara-Padilla E, Ceballos-Reyes G, Canto P, Palma-Flores C, Coral-Vázquez RM.  Biochimie. 2012 Sep;94(9):1884-90. doi: 10.1016/j.biochi.2012.05.001

 

Role of microRNAs in central nervous system development and pathology. Meza-Sosa KF, Valle-García D, Pedraza-Alva G, Pérez-Martínez L. J Neurosci Res. 2012 Jan;90(1):1-12. doi: 10.1002/jnr.22701.

 

Identification of a disulfide bridge essential for structure and function of the voltage-gated Ca(2+) channel α(2)δ-1 auxiliary subunit.Calderón-Rivera A, Andrade A, Hernández-Hernández O, González-Ramírez R, Sandoval A, Rivera M, Gomora JC, Felix R. Cell Calcium. 2012; 51(1):22-30.

 

Myotonic dystrophy type 1-associated CTG repeats disturb the expression and subcellular distribution of microtubule-associated proteins MAP1A, MAP2, and MAP6/STOP in PC12 cells. Velázquez-Bernardino P, García-Sierra F, Hernández-Hernández O, Bermúdez de León M, Gourdon G, Gomes-Pereira M, Cisneros B.

Molecular Biology Reports. 2012; 39(1):415-24

 

2011

 

Signaling epigenetics: novel insights on cell signaling and epigenetic regulation.

Arzate-Mejía RG, Valle-García D, Recillas-Targa F. IUBMB Life. 2011 Oct;63(10):881-95. doi: 10.1002/iub.557.

 

 

2010

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Identical repeated backbone of the human genome. Zepeda-Mendoza CJ, Lemus T, Yáñez O, García D, Valle-García D, Meza-Sosa KF, Gutiérrez-Arcelus M, Márquez-Ortiz Y, Domínguez-Vidaña R, Gonzaga-Jauregui C, Flores M, Palacios R. BMC Genomics. 2010 Jan 23;11:60. doi: 10.1186/1471-2164-11-60.

 

Recombinant human ZP3-induced sperm acrosome reaction: evidence for the involvement of T- and L-type voltage-gated calcium channels. José O, Hernández-Hernández O, Chirinos M, González-González ME, Larrea F, Almanza A, Felix R, Darszon A, Treviño CL. Biochemical and Biophysical Research Communications. 2010; 395(4):530-4.

 

2009

 

Sox9 represses alpha-sarcoglycan gene expression in early myogenic differentiation. Hernández-Hernández JM, Delgado-Olguín P, Aguillón-Huerta V, Furlan-Magaril M, Recillas-Targa F, Coral-Vázquez RM. J Mol Biol. 2009 Nov 20;394(1):1-14. doi: 10.1016/j.jmb.2009.08.057.

2008

 

Identification of two E-boxes that negatively modulate the activity of MyoD on the alpha-sarcoglycan core promoter. Delgado-Olguín P, Hernández-Hernández JM, Salamanca F, Recillas-Targa F, Coral-Vázquez RM. Biochim Biophys Acta. 2008 Jan;1779(1):74-80.

 

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. Cellular and Molecular Neurobiology. 2009; 29(8):1265-73. 

 

2008

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Histamine-induced Ca2+ entry in human astrocytoma U373 MG cells: evidence for involvement of store-operated channels. Barajas M, Andrade A, Hernandez-Hernandez O, Felix R, Arias-Montaño JA. Journal of Neuroscience Research. 2008; 86(15):3456-68.

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2007

 

Dysferlin homozygous mutation G1418D causes limb-girdle type 2B in a Mexican family. Rosas-Vargas H, Gómez-Díaz B, Ruano-Calderón L, Fernández-Valverde F, Roque-Ramírez B, Portillo-Bobadilla T, Ordoñez-Razo RM, Minauro-Sanmiguel F, Coral-Vázquez R. Genet Test. 2007 Winter;11(4):391-6. doi: 10.1089/gte.2007.0039.

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Myotonic dystrophy CTG repeat expansion alters Ca2+ channel functional expression in PC12 cells. Andrade A, de León MB, Hernández-Hernández O, Cisneros B, Felix R. FEBS Letters. 2007; 581(23):4430-8. 

 

2006

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A novel isoform of delta-sarcoglycan is localized at the sarcoplasmic reticulum of mouse skeletal muscle. Estrada FJ, Mornet D, Rosas-Vargas H, Angulo A, Hernández M, Becker V, Rendón A, Ramos-Kuri M, Coral-Vázquez RM. Biochem Biophys Res Commun. 2006 Feb 17;340(3):865-71. 

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Myotonic dystrophy expanded CUG repeats disturb the expression and phosphorylation of tau in PC12 cells. Hernández-Hernández O, Bermúdez-de-León M, Gómez P, Velázquez-Bernardino P, García-Sierra F, Cisneros B. Journal of Neuroscience Research. 2006; 84(4):841-51.