Abasolo N - Search Results

1

Association study between polymorphims in GAS6-TAM genes and carotid atherosclerosis.

Hurtado B, Abasolo N, Muñoz X, García N, Benavente Y, Rubio F, García de Frutos P, Krupinski J, Sala N. Hurtado B, et al. Among authors: abasolo n. Thromb Haemost. 2010 Sep;104(3):592-8. doi: 10.1160/TH09-11-0787. Epub 2010 Jul 20. Thromb Haemost. 2010. PMID: 20664904

2

First case of protein S deficiency due to a translocation t(3;21)(q11.2;q22).

Hurtado B, Nadal M, Margarit E, Sánchez A, Abasolo N, García N, Doménech P, Sala N. Hurtado B, et al. Among authors: abasolo n. Thromb Haemost. 2009 May;101(5):977-9. Thromb Haemost. 2009. PMID: 19404554 No abstract available.

3

Confirmation of inherited protein S deficiency by PROS1 mutational screening: Identification of three novel PROS1 mutations and haplotype analysis of p.Q279X recurrence.

Hurtado B, Abasolo N, Domènech-Santasusana P, Fuentes-Prior P, García de Frutos P, Sala N. Hurtado B, et al. Among authors: abasolo n. Thromb Haemost. 2008 Oct;100(4):721-4. Thromb Haemost. 2008. PMID: 18841302 No abstract available.

4

No evidence that major mtDNA European haplogroups confer risk to schizophrenia.

Mosquera-Miguel A, Torrell H, Abasolo N, Arrojo M, Paz E, Ramos-Ríos R, Agra S, Páramo M, Brenlla J, Martínez S, Vilella E, Valero J, Gutiérrez-Zotes A, Martorell L, Costas J, Salas A. Mosquera-Miguel A, et al. Among authors: abasolo n. Am J Med Genet B Neuropsychiatr Genet. 2012 Jun;159B(4):414-21. doi: 10.1002/ajmg.b.32044. Epub 2012 Mar 29. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22467472

5

Mitochondrial DNA (mtDNA) in brain samples from patients with major psychiatric disorders: gene expression profiles, mtDNA content and presence of the mtDNA common deletion.

Torrell H, Montaña E, Abasolo N, Roig B, Gaviria AM, Vilella E, Martorell L. Torrell H, et al. Among authors: abasolo n. Am J Med Genet B Neuropsychiatr Genet. 2013 Mar;162B(2):213-23. doi: 10.1002/ajmg.b.32134. Epub 2013 Jan 25. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23355257

6

Mitochondrial DNA (mtDNA) variants in the European haplogroups HV, JT, and U do not have a major role in schizophrenia.

Torrell H, Salas A, Abasolo N, Morén C, Garrabou G, Valero J, Alonso Y, Vilella E, Costas J, Martorell L. Torrell H, et al. Among authors: abasolo n. Am J Med Genet B Neuropsychiatr Genet. 2014 Oct;165B(7):607-17. doi: 10.1002/ajmg.b.32264. Epub 2014 Aug 17. Am J Med Genet B Neuropsychiatr Genet. 2014. PMID: 25132006

7

Discoidin domain receptor 1 gene variants are associated with decreased white matter fractional anisotropy and decreased processing speed in schizophrenia.

Gas C, Canales-Rodríguez EJ, Radua J, Abasolo N, Cortés MJ, Salvadó E, Muntané G, Alemán-Gómez Y, Julià T, Marsal S, Sanjuan J, Guitart M, Costas J, Martorell L, Pomarol-Clotet E, Vilella E. Gas C, et al. Among authors: abasolo n. J Psychiatr Res. 2019 Mar;110:74-82. doi: 10.1016/j.jpsychires.2018.12.021. Epub 2018 Dec 24. J Psychiatr Res. 2019. PMID: 30597424

8

Increased expression of the spliced DDR1c isoform in brain tissues from schizophrenia patients.

Roig B, Abasolo N, Moyano S, Martorell L, Vilella E. Roig B, et al. Among authors: abasolo n. J Psychiatr Res. 2012 Jun;46(6):825-7. doi: 10.1016/j.jpsychires.2012.02.018. Epub 2012 Mar 14. J Psychiatr Res. 2012. PMID: 22421314 No abstract available.

9

RT-qPCR study on post-mortem brain samples from patients with major psychiatric disorders: reference genes and specimen characteristics.

Abasolo N, Torrell H, Roig B, Moyano S, Vilella E, Martorell L. Abasolo N, et al. J Psychiatr Res. 2011 Nov;45(11):1411-8. doi: 10.1016/j.jpsychires.2011.06.001. Epub 2011 Jun 24. J Psychiatr Res. 2011. PMID: 21704324

10

Genetic and clinical evidence of mitochondrial dysfunction in autism spectrum disorder and intellectual disability.

Valiente-Pallejà A, Torrell H, Muntané G, Cortés MJ, Martínez-Leal R, Abasolo N, Alonso Y, Vilella E, Martorell L. Valiente-Pallejà A, et al. Among authors: abasolo n. Hum Mol Genet. 2018 Mar 1;27(5):891-900. doi: 10.1093/hmg/ddy009. Hum Mol Genet. 2018. PMID: 29340697

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