MARÍA ESTHER
FAREZ VIDAL
CATEDRÁTICA DE UNIVERSIDAD
JOSÉ ANTONIO
GÓMEZ CAPILLA
Ikertzailea 2015-2016 tartean
JOSÉ ANTONIO GÓMEZ CAPILLA-rekin lankidetzan egindako argitalpenak (12)
2013
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Differential immunohistochemical localization of desmosomal plaque-related proteins in non-small-cell lung cancer
Histopathology, Vol. 63, Núm. 1, pp. 103-113
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Influence of CYP2D6 polymorphisms on serum levels of tamoxifen metabolites in Spanish women with breast cancer
International Journal of Medical Sciences, Vol. 10, Núm. 7, pp. 932-937
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Survival, classifications, and desmosomal plaque genes in non-small cell lung cancer
International Journal of Medical Sciences, Vol. 10, Núm. 9, pp. 1166-1173
2012
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Multiplex primer extension reaction and capillary electrophoresis to study the frequency of thrombophilia-related mutations in a spanish population
Clinica Chimica Acta, Vol. 413, Núm. 15-16, pp. 1255-1258
2011
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Gene expression profiling reveals novel biomarkers in nonsmall cell lung cancer
International Journal of Cancer, Vol. 129, Núm. 2, pp. 355-364
2010
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Gene expression signatures in breast cancer distinguish phenotype characteristics, histologic subtypes, and tumor invasiveness
Cancer, Vol. 116, Núm. 2, pp. 486-496
2008
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A family with atypical cystic fibrosis: brother and sister with heterozygosity for both G542X and R117H
Pediatric and Developmental Pathology, Vol. 11, Núm. 3, pp. 213-219
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Multi-mutational analysis of fifteen common mutations of the glucose 6-phosphate dehydrogenase gene in the Mediterrranean population
Clinica Chimica Acta, Vol. 395, Núm. 1-2, pp. 94-98
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Use of capillary electrophoresis for accurate determination of CAG repeats causing Huntington disease. An oligonucleotide design avoiding shadow bands
Scandinavian Journal of Clinical and Laboratory Investigation, Vol. 68, Núm. 7, pp. 577-584
2005
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Frequency and clinical expression of HFE gene mutations in a Spanish population of subjects with abnormal iron metabolism
Annals of Hematology, Vol. 84, Núm. 10, pp. 650-655
2004
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Multimutational analysis of eleven cystic fibrosis mutations common in the Mediterranean areas
Clinical Chemistry, Vol. 50, Núm. 11, pp. 2155-2157
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Multiplex analysis of the most common mutations related to hereditary haemochromatosis: Two methods combining specific amplification with capillary electrophoresis
European Journal of Haematology, Vol. 72, Núm. 2, pp. 121-129