Porta S - Search Results

1

A pathogenic mechanism in Huntington's disease involves small CAG-repeated RNAs with neurotoxic activity.

Bañez-Coronel M, Porta S, Kagerbauer B, Mateu-Huertas E, Pantano L, Ferrer I, Guzmán M, Estivill X, Martí E. Bañez-Coronel M, et al. Among authors: porta s. PLoS Genet. 2012;8(2):e1002481. doi: 10.1371/journal.pgen.1002481. Epub 2012 Feb 23. PLoS Genet. 2012. PMID: 22383888 Free PMC article.

2

A myriad of miRNA variants in control and Huntington's disease brain regions detected by massively parallel sequencing.

Martí E, Pantano L, Bañez-Coronel M, Llorens F, Miñones-Moyano E, Porta S, Sumoy L, Ferrer I, Estivill X. Martí E, et al. Among authors: porta s. Nucleic Acids Res. 2010 Nov;38(20):7219-35. doi: 10.1093/nar/gkq575. Epub 2010 Jun 30. Nucleic Acids Res. 2010. PMID: 20591823 Free PMC article.

3

RCAN1 (DSCR1) increases neuronal susceptibility to oxidative stress: a potential pathogenic process in neurodegeneration.

Porta S, Serra SA, Huch M, Valverde MA, Llorens F, Estivill X, Arbonés ML, Martí E. Porta S, et al. Hum Mol Genet. 2007 May 1;16(9):1039-50. doi: 10.1093/hmg/ddm049. Epub 2007 Mar 6. Hum Mol Genet. 2007. PMID: 17341486

4

MicroRNA profiling of Parkinson's disease brains identifies early downregulation of miR-34b/c which modulate mitochondrial function.

Miñones-Moyano E, Porta S, Escaramís G, Rabionet R, Iraola S, Kagerbauer B, Espinosa-Parrilla Y, Ferrer I, Estivill X, Martí E. Miñones-Moyano E, et al. Among authors: porta s. Hum Mol Genet. 2011 Aug 1;20(15):3067-78. doi: 10.1093/hmg/ddr210. Epub 2011 May 10. Hum Mol Genet. 2011. PMID: 21558425

5

Upregulation of a small vault RNA (svtRNA2-1a) is an early event in Parkinson disease and induces neuronal dysfunction.

Miñones-Moyano E, Friedländer MR, Pallares J, Kagerbauer B, Porta S, Escaramís G, Ferrer I, Estivill X, Martí E. Miñones-Moyano E, et al. Among authors: porta s. RNA Biol. 2013 Jul;10(7):1093-106. doi: 10.4161/rna.24813. Epub 2013 May 1. RNA Biol. 2013. PMID: 23673382 Free PMC article.

6

Differential expression of members of the RCAN family of calcineurin regulators suggests selective functions for these proteins in the brain.

Porta S, Martí E, de la Luna S, Arbonés ML. Porta S, et al. Eur J Neurosci. 2007 Sep;26(5):1213-26. doi: 10.1111/j.1460-9568.2007.05749.x. Eur J Neurosci. 2007. PMID: 17767500

7

Increased striatal adenosine A2A receptor levels is an early event in Parkinson's disease-related pathology and it is potentially regulated by miR-34b.

Villar-Menéndez I, Porta S, Buira SP, Pereira-Veiga T, Díaz-Sánchez S, Albasanz JL, Ferrer I, Martín M, Barrachina M. Villar-Menéndez I, et al. Among authors: porta s. Neurobiol Dis. 2014 Sep;69:206-14. doi: 10.1016/j.nbd.2014.05.030. Epub 2014 Jun 2. Neurobiol Dis. 2014. PMID: 24892887

8

DSCR1/RCAN1 regulates vesicle exocytosis and fusion pore kinetics: implications for Down syndrome and Alzheimer's disease.

Keating DJ, Dubach D, Zanin MP, Yu Y, Martin K, Zhao YF, Chen C, Porta S, Arbonés ML, Mittaz L, Pritchard MA. Keating DJ, et al. Among authors: porta s. Hum Mol Genet. 2008 Apr 1;17(7):1020-30. doi: 10.1093/hmg/ddm374. Epub 2008 Jan 7. Hum Mol Genet. 2008. PMID: 18180251

9

Over-expression of RCAN1 causes Down syndrome-like hippocampal deficits that alter learning and memory.

Martin KR, Corlett A, Dubach D, Mustafa T, Coleman HA, Parkington HC, Merson TD, Bourne JA, Porta S, Arbonés ML, Finkelstein DI, Pritchard MA. Martin KR, et al. Among authors: porta s. Hum Mol Genet. 2012 Jul 1;21(13):3025-41. doi: 10.1093/hmg/dds134. Epub 2012 Apr 17. Hum Mol Genet. 2012. PMID: 22511596

10

Neuronal hemoglobin is reduced in Alzheimer's disease, argyrophilic grain disease, Parkinson's disease, and dementia with Lewy bodies.

Ferrer I, Gómez A, Carmona M, Huesa G, Porta S, Riera-Codina M, Biagioli M, Gustincich S, Aso E. Ferrer I, et al. Among authors: porta s. J Alzheimers Dis. 2011;23(3):537-50. doi: 10.3233/JAD-2010-101485. J Alzheimers Dis. 2011. PMID: 21157025 Free article.

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