Bello M.J.
42
Coauthors
5
Documentos
Volumen de publicaciones por año
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Año de publicación | Num. Publicaciones |
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1995 | 2 |
1998 | 1 |
1999 | 2 |
Publicaciones por áreas de conocimiento
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Área de conocimiento | Num. Publicaciones |
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Genética | 5 |
Cáncer | 4 |
Patología | 1 |
Publicaciones por áreas temáticas
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Área temática | Num. Publicaciones |
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Enfermedades | 5 |
Anatomía humana, citología, histología | 2 |
Principales fuentes de datos
Origen | Num. Publicaciones |
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Scopus | 5 |
Google Scholar | 4 |
RRAAE | 0 |
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Coautores destacados por número de publicaciones
Coautor | Num. Publicaciones |
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Pestana A. | 5 |
Rey J.A. | 5 |
Paola E. Leone | 5 |
de Campos J.M. | 5 |
Sarasa J.L. | 5 |
Vaquero J. | 5 |
Kusak M.E. | 3 |
Nebreda P. | 2 |
Mendiola M. | 2 |
Queizan A. | 1 |
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Publicaciones del autor
NF2 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: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:scopusSix 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: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: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:googlescopus