Persistence of androgenic effects on the production of proinflammatory cytokines by circulating antigen-presenting cells after withdrawal of testosterone treatment in aging type 2 diabetic men with partial androgen deficiency Corrales JJ, Almeida M, Miralles JM, Orfao A. Fertility and Sterility 92:311-319. FI: 3.970 (Q1) Análisis genético (PKD2) de la poliquistosis renal autosómica dominante Gómez PF, Moro EC, García-Cosmes P, Sarmiento RG, Romo JM. Nefrología 29:562-568. FI: 0.533 (Q4) The G1359A-CNR1 gene polymorphism is associated to glioma in Spanish patients Núñez M, Perdomo S, Moreta J, Santos-Briz A, González-Sarmiento R. Clinical & Translational Oncology 12:825-828. FI: 1.146 (Q4) Molecular analysis of congenital goitres with hypothyroidism caused by defective thyroglobulin synthesis. Identification of a novel c.7006C>T [p.R2317X] mutation and expression of minigenes containing nonsense mutations in exon 7 Machiavelli GA, Caputo M, Rivolta CM, Olcese MC, Gruñeiro-Papendieck L, Chiesa A, González-Sarmiento R, Targovnik HM. Clinical Endocrinology 72:112-121. FI: 3.201 (Q2) Analysis of the STS gene in 40 patients with recessive X-linked ichthyosis: a high frequency of partial deletions in a Spanish population Cañueto J, Ciria S, Hernández-Martín A, Unamuno P, González-Sarmiento R. Journal of the European Academy of 24(10):1226-1229. FI: 2.787 (Q1) X-linked ichthyosis along with recessive dystrophic epidermolysis bullosa in the same patient Hernández-Martín A, Cuadrado-Corrales N, Ciria-Abad S, Arias-Palomo D, Mascaró-Galy JM, Escámez MJ, García M, Del Río M, Torrelo A, González-Sarmiento R. Dermatology 221(2):113-116. FI: 2.741 (Q2) Approach to early-onset colorectal cancer: clinicopathological, familial, molecular and immunohistochemical characteristics Perea J, Álvaro E, Rodríguez Y, Gravalos C, Sánchez-Tomé E, Rivera B, Colina F, Carbonell P, González-Sarmiento R, Hidalgo M, Urioste M. World Journal of Gastroenterology 16:3697-3703. FI: 2.092 (Q3) Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone Albagha OM, Visconti MR, Alonso N, Langston AL, Cundy T, Dargie R, Dunlop MG, Fraser WD, Hooper MJ, Isaia G, Nicholson GC, del Pino Montes J, González-Sarmiento R, di Stefano M, Tenesa A, Walsh JP, Ralston SH. Nature Genetics 42:520-524. FI: 34.284 (Q1) Paget's disease of bone is not associated with common polymorphisms in interleukin-6, interleukin-8 and tumor necrosis factor alpha genes Corral-Gudino L, del Pino-Montes J, García-Aparicio J, Alonso-Garrido M, González-Sarmiento R. Cytokine 52:146-150. FI: 3.123 (Q3) Molecular analysis of ex-vivo CD133. GBM cells revealed a common invasive and angiogenic profile but different proliferative signatures among high grade gliomas García JL, Pérez-Caro M, Gómez-Morete JA, González F, Ortiz J, Blanco O, Sancho M, Hernández-Rivas JM, González-Sarmiento R, Sánchez-Martin M. BMC Cancer 10:454. FI: 2.736 (Q2)
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