Ruiz del Río, N.; Abelairas Gómez, J.M.; Alonso García de la Rosa, F.J.; Peralta Calvo, J.M.; de las Heras Martín, A. "[Genetic analysis results of patients with a retinoblastoma refractory to systemic chemotherapy].". Arch Soc Esp Oftalmol. 90(9): 414-420. (2015). (PMID: 25817468).
Ruiz Del Río, N.; Abelairas Gómez, J.M.; Alonso García de la Rosa, F.J.; Peralta Calvo, J.M.; de Las Heras Martín, A. "[Trilateral retinoblastoma. Correlation between the genetic anomalies of the RB1 gene and the presence of pineal gland cysts].". Arch Soc Esp Oftalmol. 89(1): 4-9. (2014). (PMID: 24269417).
Gómez-Cabello, D.; Callejas, S.; Benguría, A.; Moreno, A.; Alonso, J.; Palmero, I. "Regulation of the microRNA processor DGCR8 by the tumor suppressor ING1.". Cancer Res.. 70(5): 1866-1874. (2010). (PMID: 20179197).
Navarro, D.; Agra, N.; Pestaña, A.; Alonso, J.; González-Sancho, J.M. "The EWS/FLI1 oncogenic protein inhibits expression of the Wnt inhibitor DICKKOPF-1 gene and antagonizes beta-catenin/TCF-mediated transcription.". Carcinogenesis. 31(3): 394-401. (2010). (PMID: 20019092).
Carrillo, J.; Agra, N.; Fernández, N.; Pestaña, A.; Alonso, J. "Devazepide, a nonpeptide antagonist of CCK receptors, induces apoptosis and inhibits Ewing tumor growth.". Anticancer Drugs. 20(7): 527-533. (2009). (PMID: 19407653).
García-Aragoncillo, E.; Carrillo, J.; Lalli, E.; Agra, N.; Gómez-López, G.; Pestaña, A.; Alonso, J. "DAX1, a direct target of EWS/FLI1 oncoprotein, is a principal regulator of cell-cycle progression in Ewing's tumor cells.". Oncogene. 27(46): 6034-6043. (2008). (PMID: 18591936).
Villamón, E.; Piqueras, M.; Mackintosh, C.; Alonso, J.; de Alava, E.; Navarro, S.; Noguera, R. "Comparison of different techniques for the detection of genetic risk-identifying chromosomal gains and losses in neuroblastoma.". Virchows Arch.. 453(1): 47-55. (2008). (PMID: 18574593).
Kontic, M.; Palacios, I.; Gámez, A.; Camino, I.; Latkovic, Z.; Rasic, D.; Krstic, V.; Bunjevacki, V.; Alonso, J.; Pestaña, A. "New RB1 oncogenic mutations and intronic polymorphisms in Serbian retinoblastoma patients: genetic counseling implications.". J. Hum. Genet.. 51(10): 909-913. (2006). (PMID: 16972022).
Alonso, J.; Palacios, I.; Gámez, A.; Camino, I.; Frayle, H.; Menéndez, I.; Kontic, M.; García-Miguel, P.; Sastre, A.; Abelairas, J.; Sarret, E.; Sabado, C.; Navajas, A.; Artigas, M.; Indiano, J.M.; Carbone, A.; Rosell, J.; Pestaña, A. "[Molecular diagnosis of retinoblastoma: molecular epidemiology and genetic counseling].". Med Clin (Barc). 126(11): 401-405. (2006). (PMID: 16595082).
Mendiola, M.; Carrillo, J.; García, E.; Lalli, E.; Hernández, T.; de Alava, E.; Tirode, F.; Delattre, O.; García-Miguel, P.; López-Barea, F.; Pestaña, A.; Alonso, J. "The orphan nuclear receptor DAX1 is up-regulated by the EWS/FLI1 oncoprotein and is highly expressed in Ewing tumors.". Int J Cancer. 118(6): 1381-1389. (2006). (PMID: 16206264).
Alonso, J.; Frayle, H.; Menéndez, I.; López, A.; García-Miguel, P.; Abelairas, J.; Sarret, E.; Vendrell, M.T.; Navajas, A.; Artigas, M.; Indiano, J.M.; Carbone, A.; Torrenteras, C.; Palacios, I.; Pestaña, A. "Identification of 26 new constitutional RB1 gene mutations in Spanish, Colombian, and Cuban retinoblastoma patients.". Hum. Mutat.. 25(1): 99. (2005). (PMID: 15605413).
Alonso, J.; Menéndez, I.; López, A.; Frayle, H.; Ruisánchez, N.; Pestaña, A. "Two independent RB1-inactivating mutations in peripheral blood DNA of a hereditary retinoblastoma patient.". Genes Chromosomes Cancer. 40(3): 271-275. (2004). (PMID: 15139006).
Leone, P.E.; Vega, M.E.; Jervis, P.; Pestaña, A.; Alonso, J.; Paz-y-Miño, C. "Two new mutations and three novel polymorphisms in the RB1 gene in Ecuadorian patients.". J. Hum. Genet.. 48(12): 639-641. (2003). (PMID: 14625809).
Leone, P.E.; Mendiola, M.; Alonso, J.; Paz-y-Miño, C.; Pestaña, A. "Implications of a RAD54L polymorphism (2290C/T) in human meningiomas as a risk factor and/or a genetic marker.". BMC Cancer. 3(): 6. (2003). (PMID: 12614485).
Alonso, J.; Moreno, C.; López, A.; Mendiola, M.; García-Miguel, P.; Abelairas, J.; Sarret, E.; Vendrell, M.T.; Navajas, A.; Pestaña, A. "Five novel single nucleotide polymorphisms of the RB1 gene (g.5625T>C, g.70169T>G, g.76875A>T, g.78026delA, and g.150072T>C) in retinoblastoma patients.". Hum. Mutat.. 17(5): 437. (2001). (PMID: 11317369).
Alonso, J.; García-Miguel, P.; Abelairas, J.; Mendiola, M.; Sarret, E.; Vendrell, M.T.; Navajas, A.; Pestaña, A. "Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients: Phenotypic and molecular epidemiological implications.". Hum. Mutat.. 17(5): 412-422. (2001). (PMID: 11317357).
Alonso, J.; García-Miguel, P.; Abelairas, J.; Mendiola, M.; Pestaña, A. "A microsatellite fluorescent method for linkage analysis in familial retinoblastoma and deletion detection at the RB1 locus in retinoblastoma and osteosarcoma.". Diagn. Mol. Pathol.. 10(1): 9-14. (2001). (PMID: 11277399).
Alonso, J.; García-Miguel, P.; Abelairas, J.; Pestaña, A. "A novel complex mutation in exon 8 of RB1 in a case of isolated bilateral retinoblastoma.". Hum. Mutat.. 15(6): 583. (2000). (PMID: 10862099).
Mendiola, M.; Bello, M.J.; Alonso, J.; Leone, P.E.; Vaquero, J.; Sarasa, J.L.; Kusak, M.E.; De Campos, J.M.; Pestaña, A.; Rey, J.A. "Search for mutations of the hRAD54 gene in sporadic meningiomas with deletion at 1p32.". Mol. Carcinog.. 24(4): 300-304. (1999). (PMID: 10326867).
Instituto de Investigaciones Biomédicas "Alberto Sols"
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