Publicacións (158) Publicacións nas que participase algún/ha investigador/a

2011

  1. 'progress' renders detrimental an ancient mitochondrial DNA genetic variant

    Human Molecular Genetics, Vol. 20, Núm. 21, pp. 4224-4231

  2. A SNP multiplex for the simultaneous prediction of biogeographic ancestry and pigmentation type

    Forensic Science International: Genetics Supplement Series, Vol. 3, Núm. 1

  3. A new drug nanocarrier consisting of polyarginine and hyaluronic acid

    European Journal of Pharmaceutics and Biopharmaceutics, Vol. 79, Núm. 1, pp. 54-57

  4. A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy

    Neuromuscular Disorders, Vol. 21, Núm. 4, pp. 254-262

  5. A novel cardioprotective p38-MAPK/mTOR pathway

    Experimental Cell Research, Vol. 317, Núm. 20, pp. 2938-2949

  6. A novel mutation in the OFD1 (Cxorf5) gene may contribute to oral phenotype in patients with oral-facial-digital syndrome type 1

    Oral Diseases, Vol. 17, Núm. 6, pp. 610-614

  7. A pharmacogenetics study of TPMT and ITPA genes detects a relationship with side effects and clinical response in patients with inflammatory bowel disease receiving azathioprine

    Journal of Gastrointestinal and Liver Diseases, Vol. 20, Núm. 3, pp. 247-253

  8. A study of East Timor variability using the SNPforID 52-plex SNP panel

    Forensic Science International: Genetics, Vol. 5, Núm. 1

  9. A two-phase case-control study for colorectal cancer genetic susceptibility: Candidate genes from chromosomal regions 9q22 and 3q22

    British Journal of Cancer, Vol. 105, Núm. 6, pp. 870-875

  10. Acetylation is indispensable for p53 antiviral activity

    Cell Cycle, Vol. 10, Núm. 21, pp. 3701-3705

  11. Aging, angiotensin system and dopaminergic degeneration in the substantia nigra

    Aging and Disease, Vol. 2, Núm. 3, pp. 257-274

  12. Aliskiren affects fatty-acid uptake and lipid-related genes in rodent and human cardiomyocytes

    Biochemical Pharmacology, Vol. 82, Núm. 5, pp. 491-504

  13. Alteraciones inmunológicas y de los valores de selectinas en pacientes hipertensos tratados según criterios actuales

    Medicina Clinica, Vol. 137, Núm. 6, pp. 254-256

  14. An update of in Silico tools for the prediction of pathogenesis in Missense variants

    Current Bioinformatics, Vol. 6, Núm. 2, pp. 185-198

  15. Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): Evidence of founder effects

    British Journal of Dermatology, Vol. 165, Núm. 4, pp. 906-911

  16. Analysis of global variability in 15 established and 5 new European Standard Set (ESS) STRs using the CEPH human genome diversity panel

    Forensic Science International: Genetics, Vol. 5, Núm. 3, pp. 155-169

  17. Anticoagulation prescription in atrial fibrillation

    Expert Opinion on Pharmacotherapy, Vol. 12, Núm. 10, pp. 1473-1479

  18. Association of Rex-1 to target genes supports its interaction with Polycomb function

    Stem Cell Research, Vol. 7, Núm. 1, pp. 1-16

  19. Biliopancreatic diversion induces villi elongation and cholecystokinin and ghrelin increase

    Diabetes and Metabolic Syndrome: Clinical Research and Reviews, Vol. 5, Núm. 2, pp. 66-70

  20. Biventricular pacing in hypertrophic obstructive cardiomyopathy: A pilot study

    Heart Rhythm, Vol. 8, Núm. 2, pp. 221-227