Publikationen (63) Publikationen, an denen Forscher/innen teilgenommen haben

2018

  1. Gating mechanism of Kv11.1 (hERG) K + channels without covalent connection between voltage sensor and pore domains

    Pflugers Archiv European Journal of Physiology, Vol. 470, Núm. 3, pp. 517-536

  2. A one-step TaqMan real-time qRT-PCR assay for the specific detection and quantitation of the Spanish goat encephalitis virus (SGEV)

    Journal of Virological Methods, Vol. 255, pp. 98-100

  3. Ablation of the stress protease OMA1 protects against heart failure in mice

    Science Translational Medicine, Vol. 10, Núm. 434

  4. Aging in the Cardiovascular System: Lessons from Hutchinson-Gilford Progeria Syndrome

    Annual Review of Physiology, Vol. 80, pp. 27-48

  5. Altered patterns of global protein synthesis and translational fidelity in RPS15-mutated chronic lymphocytic leukemia

    Blood, Vol. 132, Núm. 22, pp. 2375-2388

  6. An altered gene expression profile in tyramine-exposed intestinal cell cultures supports the genotoxicity of this biogenic amine at dietary concentrations

    Scientific Reports, Vol. 8, Núm. 1

  7. Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer

    Gastroenterology, Vol. 154, Núm. 1, pp. 181-194.e20

  8. Biomarkers and polymorphisms in pancreatic neuroendocrine tumors treated with sunitinib

    Oncotarget, Vol. 9, Núm. 97, pp. 36894-36905

  9. Cancertool: A visualization and representation interface to exploit cancer datasets

    Cancer Research, Vol. 78, Núm. 21, pp. 6320-6328

  10. Carbotoxicity—Noxious Effects of Carbohydrates

    Cell, Vol. 175, Núm. 3, pp. 605-614

  11. Changes at the nuclear lamina alter binding of pioneer factor Foxa2 in aged liver

    Aging Cell, Vol. 17, Núm. 3

  12. Chronic lymphocytic leukemia and mantle cell lymphoma: Crossroads of genetic and microenvironment interactions

    Blood, Vol. 131, Núm. 21, pp. 2283-2296

  13. Clinical course and pathogenicity of variant rabbit haemorrhagic disease virus in experimentally infected adult and kit rabbits: Significance towards control and spread

    Veterinary Microbiology, Vol. 220, pp. 24-32

  14. Clinical impact of the subclonal architecture and mutational complexity in chronic lymphocytic leukemia

    Leukemia, Vol. 32, Núm. 3, pp. 645-653

  15. Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients

    BMC Medical Genomics, Vol. 11, Núm. 1

  16. Conventional and real time RT-PCR assays for the detection and differentiation of variant rabbit hemorrhagic disease virus (RHDVb) and its recombinants

    Journal of Virological Methods, Vol. 251, pp. 118-122

  17. Decapping protein EDC4 regulates DNA repair and phenocopies BRCA1

    Nature Communications, Vol. 9, Núm. 1

  18. Disruption of the beclin 1-BCL2 autophagy regulatory complex promotes longevity in mice

    Nature, Vol. 558, Núm. 7708, pp. 136-140

  19. Does Simultaneous Administration of Bivalent (Types 1 and 3) Oral Poliovirus Vaccine and Inactivated Poliovirus Vaccine Induce Mucosal Cross-immunity to Poliovirus Type 2?

    Clinical Infectious Diseases, Vol. 67, pp. S51-S56

  20. ELISA for detection of variant rabbit haemorrhagic disease virus RHDV2 antigen in liver extracts

    Journal of Virological Methods, Vol. 251, pp. 38-42