Moreno-Pelayo MA - Search Results

1

Therapeutic Potential of EWSR1-FLI1 Inactivation by CRISPR/Cas9 in Ewing Sarcoma.

Cervera ST, Rodríguez-Martín C, Fernández-Tabanera E, Melero-Fernández de Mera RM, Morin M, Fernández-Peñalver S, Iranzo-Martínez M, Amhih-Cardenas J, García-García L, González-González L, Moreno-Pelayo MA, Alonso J. Cervera ST, et al. Cancers (Basel). 2021 Jul 27;13(15):3783. doi: 10.3390/cancers13153783. Cancers (Basel). 2021. PMID: 34359682 Free PMC article.

2

A de novo missense mutation in the gene encoding the SOX10 transcription factor in a Spanish sporadic case of Waardenburg syndrome type IV.

Morín M, Viñuela A, Rivera T, Villamar M, Moreno-Pelayo MA, Moreno F, del Castillo I. Morín M, et al. Am J Med Genet A. 2008 Apr 15;146A(8):1032-7. doi: 10.1002/ajmg.a.32181. Am J Med Genet A. 2008. PMID: 18348274 No abstract available.

3

Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss.

Mencía A, Modamio-Høybjør S, Redshaw N, Morín M, Mayo-Merino F, Olavarrieta L, Aguirre LA, del Castillo I, Steel KP, Dalmay T, Moreno F, Moreno-Pelayo MA. Mencía A, et al. Nat Genet. 2009 May;41(5):609-13. doi: 10.1038/ng.355. Epub 2009 Apr 12. Nat Genet. 2009. PMID: 19363479

4

In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment.

Morín M, Bryan KE, Mayo-Merino F, Goodyear R, Mencía A, Modamio-Høybjør S, del Castillo I, Cabalka JM, Richardson G, Moreno F, Rubenstein PA, Moreno-Pelayo MA. Morín M, et al. Hum Mol Genet. 2009 Aug 15;18(16):3075-89. doi: 10.1093/hmg/ddp249. Epub 2009 May 28. Hum Mol Genet. 2009. PMID: 19477959 Free PMC article.

5

Genetic and phenotypic heterogeneity in two novel cases of Waardenburg syndrome type IV.

Viñuela A, Morín M, Villamar M, Morera C, Lavilla MJ, Cavallé L, Moreno-Pelayo MA, Moreno F, del Castillo I. Viñuela A, et al. Am J Med Genet A. 2009 Oct;149A(10):2296-302. doi: 10.1002/ajmg.a.33026. Am J Med Genet A. 2009. PMID: 19764030 No abstract available.

6

Selective miRNA Modulation Fails to Activate HIV Replication in In Vitro Latency Models.

López-Huertas MR, Morín M, Madrid-Elena N, Gutiérrez C, Jiménez-Tormo L, Santoyo J, Sanz-Rodríguez F, Moreno Pelayo MÁ, Bermejo LG, Moreno S. López-Huertas MR, et al. Mol Ther Nucleic Acids. 2019 Sep 6;17:323-336. doi: 10.1016/j.omtn.2019.06.006. Epub 2019 Jun 20. Mol Ther Nucleic Acids. 2019. PMID: 31288207 Free PMC article.

7

Three New Mutations and Mild, Asymmetrical Phenotype in the Highly Distinctive LAMM Syndrome: A Report of Eight Further Cases.

Al Yassin A, D'Arco F, Morín M, Pagarkar W, Harrop-Griffiths K, Shaida A, Fernández E, Cullup T, De-Souza B, Moreno-Pelayo MA, Bitner-Glindzicz M. Al Yassin A, et al. Genes (Basel). 2019 Jul 12;10(7):529. doi: 10.3390/genes10070529. Genes (Basel). 2019. PMID: 31336982 Free PMC article.

8

Novel mutations in the KCNJ10 gene associated to a distinctive ataxia, sensorineural hearing loss and spasticity clinical phenotype.

Morin M, Forst AL, Pérez-Torre P, Jiménez-Escrig A, Barca-Tierno V, García-Galloway E, Warth R, Lopez-Sendón Moreno JL, Moreno-Pelayo MA. Morin M, et al. Neurogenetics. 2020 Apr;21(2):135-143. doi: 10.1007/s10048-020-00605-6. Epub 2020 Feb 15. Neurogenetics. 2020. PMID: 32062759

9

Simple Protocol for Generating and Genotyping Genome-Edited Mice With CRISPR-Cas9 Reagents.

Fernández A, Morín M, Muñoz-Santos D, Josa S, Montero A, Rubio-Fernández M, Cantero M, Fernández J, Del Hierro MJ, Castrillo M, Moreno-Pelayo MÁ, Montoliu L. Fernández A, et al. Curr Protoc Mouse Biol. 2020 Mar;10(1):e69. doi: 10.1002/cpmo.69. Curr Protoc Mouse Biol. 2020. PMID: 32159922

10

A Novel Truncating Mutation in HOMER2 Causes Nonsyndromic Progressive DFNA68 Hearing Loss in a Spanish Family.

Lachgar M, Morín M, Villamar M, Del Castillo I, Moreno-Pelayo MÁ. Lachgar M, et al. Genes (Basel). 2021 Mar 12;12(3):411. doi: 10.3390/genes12030411. Genes (Basel). 2021. PMID: 33809266 Free PMC article.

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