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Allelic loss at 1p and 19q frequently occurs in association and may represent early oncogenic events in oligodendroglial tumors
ArticleAbstract: The molecular mechanisms underlying the genesis and progression of oligodendroglial tumors are poorlPalabras claves:Autores:de Campos J.M., Elena Kusak M., Josefa Bello M., Paola E. Leone, Pestana A., Rey J.A., Sarasa J.L., Vaquero J.Fuentes:googlescopusAllelic status of chromosome 1 in neoplasms of the nervous system
ArticleAbstract: By using five highly polymorphic markers, the allelic status of chromosome 1 was established in a sePalabras claves:Autores:Bello M.J., Cusak M.E., de Campos J.M., García-Miguel P., Hernández-Moneo J.L., Nebreda P., Paola E. Leone, Pestana A., Queizan A., Rey J.A., Sarasa J.L., Vaquero J.Fuentes:googlescopusSearch for mutations of the hRAD54 gene in sporadic meningiomas with deletion at 1p32
ArticleAbstract: The hRAD54 gene is related to a family of genes involved in DNA recombination and repair and encodesPalabras claves:1p deletion mapping, Allelic losses, hRAD54, Meningiomas, Tumor progressionAutores:Alonso J., Bello M.J., de Campos J.M., Kusak M.E., Mendiola M., Paola E. Leone, Pestana A., Rey J.A., Sarasa J.L., Vaquero J.Fuentes:googlescopusMolecular abnormalities of chromosome 19 in malignant gliomas: Preferential involvement of the 19q13.2-q13.4 region
ArticleAbstract: A deletion mapping analysis of chromosome 19 was performed on a series of 101 samples derived from mPalabras claves:astrocytoma, chromosome 19, glioblastoma multiforme, gliomasAutores:Bello M.J., de Campos J.M., Kusak M.E., Nebreda P., Paola E. Leone, Pestana A., Rey J.A., Sarasa J.L., Vaquero J.Fuentes:scopusNF2 gene mutations and allelic status of 1p, 14q and 22q in sporadic meningiomas
ArticleAbstract: Formation of meningiomas and their progression to malignancy may be a multi-step process, implying aPalabras claves:1p and 14q deletion mapping, Allelic losses, Meningiomas, NF2, Tumor progressionAutores:Bello M.J., de Campos J.M., Paola E. Leone, Pestana A., Rey J.A., Sarasa J.L., Vaquero J.Fuentes:googlescopusSix novel mutations in the NF2 tumor suppressor gene
ArticleAbstract: Six novel mutations were identified in the NF2 tumor suppressor gene in a panel of meningiomas and nPalabras claves:LOH 22q, MENINGIOMA, Mutations, NF2 gene, SchwannomaAutores:Bello M.J., de Campos J.M., Kusak M.E., Mendiola M., Paola E. Leone, Pestana A., Rey J.A., Sarasa J.L., Vaquero J.Fuentes:googlescopusAllelic status of 1p, 14q, and 22q and NF2 gene mutations in sporadic schwannomas.
ArticleAbstract: Schwannomas are common benign tumours of schwann cell origin, frequently found in patients with neurPalabras claves:Autores:Bello M.J., de Campos J.M., Kusak M.E., Mendiola M., Paola E. Leone, Pestana A., Rey J.A., Sarasa J.L., Vaquero J.Fuentes:scopusCharacterization of endolymphatic sac tumors and von Hippel-Lindau disease in the International Endolymphatic Sac Tumor Registry
ArticleAbstract: Background Endolymphatic sac tumors (ELSTs) are, with a prevalence of up to 16%, a component of vonPalabras claves:endolymphatic sac tumor, Prevalence, temporal bone MRI, von Hippel-LindauAutores:Angelica Malinoc, Birke Bausch, Carlos Suárez, Carsten C. Boedeker, Christian Offergeld, Claudia Hader, Claudio Letizia, de Campos J.M., Eamonn R. Maher, Elisabetta Zanoletti, Eng C., Francesca Schiavi, Frederik J. Hes, Gabriela Sansó, Hartmut P.H. Neumann, Hiroshi Kanno, Mariagiulia Anglani, Marta Barontini, Mathieu Peyre, Olivier Sterkers, Opocher G., Patrice Tran Ba Huy, Serge Bobin, Sophie Giraud, Stefan Zschiedrich, Stephane Richard, Sven Glasker, Thera Links, Tobias Krauss, Ulrich WellnerFuentes:scopus