Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Miguel Hernandez-Marti"'
Autor:
Elena Grau, Silvestre Oltra, Miguel Hernandez-Marti, José María Fernández, Francisco Martínez, Carmen Orellana, Victoria Castel, Adela Cañete
Publikováno v:
Journal of Cancer Research and Clinical Oncology. 135:523-531
Neuroblastoma is an embryonal tumor of neuroectodermal cells. Patients with metastatic neuroblastoma have a poor survival rate, which has led to numerous efforts to develop prognostic markers. Cancer/testis-specific antigens MAGE-A1 and MAGE-A3 genes
Autor:
Silvestre Oltra, Victoria Castel, Elena Grau, Francisco Martínez, Miguel Hernandez-Marti, Carmen Orellana
Publikováno v:
Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics. 15:393-398
Neuroblastoma and pheochromocytoma have the same embryonal origin. They originate from neural crest cells, and they usually affect suprarenal glands. The SDHB gene encodes the B subunit of succinate dehydrogenase, a protein implicated in the electron
Autor:
Victor Pastor Loyola, Markus Schmugge, Miguel Hernandez-Marti, Albert Català, Barbara De Moerloose, Bartlomiej P Przychodzen, Jan Starý, Roos J. Leguit, Shinsuke Hirabayashi, Riccardo Masetti, G. Kerndrup, Michael Dworzak, Vit Campr, Franco Locatelli, Marek Ussowicz, Pascale Paepe, Ingrid Simonitsch-Klupp, Maureen OxSullivan, Rita Devito, Marcin W. Wlodarski, Owen P. Smith, Marry M. van den Heuvel-Eibrink, Axel Karow, Jadwiga Maldyk, Jaroslaw P. Maciejewski, Brigitte Strahm, Irith Baumann, Emilia J Kozyra, Henrik Hasle, Charlotte M. Niemeyer
Publikováno v:
Blood. 126:1662-1662
Childhood myelodysplastic syndromes (MDS) belong to a rare group of disorders of aberrant clonal hematopoiesis manifesting throughout entire childhood and adolescence. We had previously established that GATA2 germline mutations can be considered the
Autor:
Victoria Castel, Miguel Hernandez-Marti, Adela Cañete, Francisco Martínez, Félix Prieto, Lourdes Badía, Carmen Orellana
Publikováno v:
Cancer genetics and cytogenetics. 105(2)
A search of TP53 mutations was undertaken in a series of 51 pediatric brain tumors. The only germ-line mutation was detected in a 9-year-old girl with a PNET. Her family history was unremarkable for neoplastic disease, except for the paternal grandfa
Autor:
Lourdes Badía, Victoria Castel, Miguel Hernandez-Marti, Félix Prieto, Francisco Martínez, José M. Millán, Carmen Orellana, Jose Andrés Alvarez-Garijo
Publikováno v:
Cancer genetics and cytogenetics. 102(2)
Cytogenetic and molecular analyses of primitive neuroectodermal tumors (PNETs) of the central nervous system (CNS) have demonstrated material losses of 17p, the region that contains the TP53 gene, as the most frequent abnormality. Mutations in the TP
Autor:
Asunción Paradís-Alós, Amparo Verdeguer Miralles, Lourdes Badía-Garrabou, Carmen Orellana-Alonso, Miguel Hernandez-Marti
Publikováno v:
Cancer genetics and cytogenetics. 83(1)
This report describes a chromosomal abnormality in an 8-year-old boy with renal adenocarcinoma. All tumor cells had the karyotype 46,XY, t(X;17)(p11.2;q25). This karyotype is compared with the cytogenetic descriptions of renal cell adenocarcinoma in