Javier Del Pino Montes-rekin lankidetzan egindako argitalpenak (10)

2020

  1. A mutation in p62 protein (p. R321C), associated to Paget's disease of bone, causes a blockade of autophagy and an activation of NF-kB pathway

    Bone, Vol. 133

2018

  1. Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density

    Annals of the rheumatic diseases, Vol. 77, Núm. 3, pp. 378-385

  2. Polymorphisms in genes implicated in base excision repair (BER) pathway are associated with susceptibility to Paget's disease of bone

    Bone, Vol. 112, pp. 19-23

2017

  1. Proangiogenic gene polymorphisms are associated with susceptibility to Paget's disease of bone and with its clinical features

    Clinical and experimental rheumatology

2016

  1. Association of IL1Β (-511 A/C) and IL6 (-174 G > C) polymorphisms with higher disease activity and clinical pattern of psoriatic arthritis

    Clinical Rheumatology, Vol. 35, Núm. 7, pp. 1789-1794

  2. VAV3 Gene Polymorphism Is Associated with Paget's Disease of Bone

    Genetic Testing and Molecular Biomarkers, Vol. 20, Núm. 6, pp. 335-337

2013

  1. Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease

    Journal of Bone and Mineral Research, Vol. 28, Núm. 11, pp. 2338-2346

2010

  1. Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone

    Nature Genetics, Vol. 42, Núm. 6, pp. 520-524

  2. Paget's disease of bone is not associated with common polymorphisms in interleukin-6, interleukin-8 and tumor necrosis factor alpha genes

    Cytokine, Vol. 52, Núm. 3, pp. 146-150

2006

  1. - 511 C/T IL1B gene polymorphism is associated to resistance to bisphosphonates treatment in Paget disease of bone

    Bone, Vol. 38, Núm. 4, pp. 589-594