J. D. de Campos

发表

Analysis of p73 gene in meningiomas with deletion at 1p.

M. Alonso, J. Rey, M. Bello, 2001, Cancer genetics and cytogenetics.

Search for mutations of the hRAD54 gene in sporadic meningiomas with deletion at 1p32

J. Rey, M. Bello, J. M. de Campos, 1999, Molecular carcinogenesis.

hRAD54 gene and 1p high-resolution deletion-mapping analyses in oligodendrogliomas.

J. Rey, M. Bello, J. Sarasa, 2000, Cancer genetics and cytogenetics.

High-resolution analysis of chromosome arm 1p alterations in meningioma.

J. Rey, M. Bello, J. Sarasa, 2000, Cancer genetics and cytogenetics.

Molecular analysis of chromosomh 1 abnormalities in human gliomas reveals frequent loss of 1p in oligodendroglial tumors

J. Rey, M. Bello, J. M. de Campos, 1994, International journal of cancer.

Allelic loss at 1 p is associated with tumor progression of meningiomas

J. Rey, M. Bello, J. M. de Campos, 1994, Genes, chromosomes & cancer.

Real-Time Quantitative PCR Analysis of Regions Involved in Gene Amplification Reveals Gene Overdose in Low-Grade Astrocytic Gliomas

M. Alonso, J. Rey, M. Bello, 2005, Diagnostic molecular pathology : the American journal of surgical pathology, part B.

Real-time quantitative PCR analysis of gene dosages reveals gene amplification in low-grade oligodendrogliomas.

M. Alonso, J. Rey, M. Bello, 2005, American journal of clinical pathology.

Molecular and cytogenetic analysis of chromosome 9 deletions in 75 malignant gliomas

J. Rey, M. Bello, J. M. de Campos, 1994, Genes, chromosomes & cancer.

Chromosomal patterns in human malignant astrocytomas.

J. Rey, M. Bello, J. M. de Campos, 1987, Cancer genetics and cytogenetics.

On trisomy of chromosome 7 in human gliomas.

J. Rey, M. Bello, J. M. de Campos, 1987, Cancer genetics and cytogenetics.

Promoter CpG methylation of multiple genes in pituitary adenomas: frequent involvement of caspase-8.

J. Rey, M. Bello, C. Casartelli, 2006, Oncology reports.

Molecular analysis of genomic abnormalities in human gliomas.

J. Rey, M. Bello, J. Sarasa, 1994, Cancer genetics and cytogenetics.

Abnormalities of chromosome 22 in human brain tumors determined by combined cytogenetic and molecular genetic approaches.

J. Rey, M. Bello, J. Sarasa, 1993, Cancer genetics and cytogenetics.

Mutational analysis of the CITED4 gene in glioblastomas.

J. Rey, C. Casartelli, J. M. de Campos, 2008, Cancer genetics and cytogenetics.

CpG island methylation status and mutation analysis of the RB1 gene essential promoter region and protein-binding pocket domain in nervous system tumours

M. Alonso, J. Rey, M. Bello, 2003, British Journal of Cancer.

Spontaneous carotid-cavernous fistula in osteogenesis imperfecta.

J. M. de Campos, M. Ferro, J. Burzaco, 1982, Journal of neurosurgery.

Research resource: Transcriptional profiling reveals different pseudohypoxic signatures in SDHB and VHL-related pheochromocytomas.

Agnieszka Maliszewska, Cristina Rodríguez-Antona, Gonzalo Gómez-López, 2010, Molecular endocrinology.

Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine neoplasia type 2.

S. Richard, C. Eng, H. Neumann, 2009, The Journal of clinical endocrinology and metabolism.

Propranolol reduces viability and induces apoptosis in hemangioblastoma cells from von Hippel-Lindau patients

J. M. de Campos, G. Serrano-Heras, T. Segura, 2015, Orphanet Journal of Rare Diseases.

Genome‐wide methylation analysis in vestibular schwannomas shows putative mechanisms of gene expression modulation and global hypomethylation at the HOX gene cluster

B. Meléndez, J. Rey, R. Burbano, 2015, Genes, chromosomes & cancer.

Deletion 3p in two lung adenocarcinomas metastatic to the brain.

J. Rey, M. Bello, J. M. de Campos, 1987, Cancer genetics and cytogenetics.

Aberrant promoter methylation of multiple genes in oligodendrogliomas and ependymomas.

M. Alonso, J. Rey, M. Bello, 2003, Cancer Genetics and Cytogenetics.

Frequent death-associated protein-kinase promoter hypermethylation in brain metastases of solid tumors.

M. Alonso, J. Rey, M. Bello, 2003, Oncology reports.

Microarray analysis of gene expression in vestibular schwannomas reveals SPP1/MET signaling pathway and androgen receptor deregulation

B. Meléndez, J. Rey, R. Burbano, 2013, International journal of oncology.

Aberrant CpG Island Methylation of Multiple Genes in Ependymal Tumors

J. Rey, P. González-Gómez, D. Arjona, 2004, Journal of Neuro-Oncology.

Analysis of the NF2 gene in oligodendrogliomas and ependymomas.

M. Alonso, J. Rey, M. Bello, 2002, Cancer genetics and cytogenetics.

Global expression profile in low grade meningiomas and schwannomas shows upregulation of PDGFD, CDH1 and SLIT2 compared to their healthy tissue

B. Meléndez, J. Rey, R. Burbano, 2014, Oncology reports.

Loss of chromosome 22 and absence of NF2 gene mutation in a case of multiple meningiomas.

M. Alonso, J. Rey, M. Bello, 2002, Human pathology.

Genetic and epigenetic alteration of the NF2 gene in sporadic meningiomas

Alberto Isla, M. Alonso, J. Rey, 2005, Genes, chromosomes & cancer.

DNA methylation pattern in 16 tumor-related genes in schwannomas.

J. Rey, M. Bello, J. M. de Campos, 2007, Cancer genetics and cytogenetics.

Meningeal hemangiopericytoma or hemangiopericytic meningioma? A cytogenetic and molecular analysis.

J. Rey, M. Bello, J. Sarasa, 1992, Cancer Genetics and Cytogenetics.

Loss of heterozygosity for distal markers on 22q in human gliomas

J. Rey, M. Bello, J. Sarasa, 1992, International journal of cancer.

Chromosomal involvement secondary to -22 in human meningiomas.

J. Rey, M. Bello, J. M. de Campos, 1988, Cancer genetics and cytogenetics.

Chromosomal composition of a series of 22 human low-grade gliomas.

J. Rey, M. Bello, J. M. de Campos, 1987, Cancer genetics and cytogenetics.

Epigenetic changes in pilocytic astrocytomas and medulloblastomas.

M. Alonso, J. Rey, M. Bello, 2003, International journal of molecular medicine.

Promoter hypermethylation of multiple genes in astrocytic gliomas.

M. Alonso, J. Rey, M. Bello, 2003, International journal of oncology.

Allelic status of chromosome 1 in neoplasms of the nervous system.

M. Bello, J. Sarasa, J. M. de Campos, 1995, Cancer genetics and cytogenetics.

A case of pituitary adenoma with 58 chromosomes.

J. Rey, M. Bello, J. M. de Campos, 1986, Cancer genetics and cytogenetics.

Incidence and origin of dicentric chromosomes in cultured meningiomas.

J. Rey, M. Bello, J. M. de Campos, 1988, Cancer genetics and cytogenetics.

Clonal chromosome aberrations in neurinomas

J. Rey, M. Bello, J. Sarasa, 1993, Genes, chromosomes & cancer.

Deletion and aberrant CpG island methylation of Caspase 8 gene in medulloblastoma.

M. Alonso, J. Rey, M. Bello, 2004, Oncology reports.

No evidence of INI1hSNF5 (SMARCB1) and PARVG point mutations in oligodendroglial neoplasms.

M. Alonso, J. Rey, M. Bello, 2005, Cancer genetics and cytogenetics.

CpG island methylation of tumor-related genes in three primary central nervous system lymphomas in immunocompetent patients.

M. Alonso, J. Rey, M. Bello, 2003, Cancer genetics and cytogenetics.

Characterization of endolymphatic sac tumors and von Hippel–Lindau disease in the International Endolymphatic Sac Tumor Registry

S. Richard, C. Eng, T. Krauss, 2016, Head & neck.

Cytogenetic findings in a human malignant melanoma metastatic to the brain.

J. Rey, M. Bello, J. M. de Campos, 1985, Cancer genetics and cytogenetics.

Methylation status of TP73 in meningiomas.

J. Rey, P. González-Gómez, J. Lomas, 2004, Cancer genetics and cytogenetics.

Detection of gene amplification and copy gains in brain metastases of solid tumors using quantitative real-time polymerase chain reaction.

J. Rey, A. Isla, J. Vaquero, 2008, Cancer Genetics and Cytogenetics.

Gene dosage and mutational analyses of EGFR in oligodendrogliomas.

M. Alonso, J. Rey, M. Gutiérrez, 2007, International journal of oncology.

EGFR sequence variations and real-time quantitative polymerase chain reaction analysis of gene dosage in brain metastases of solid tumors.

J. Rey, D. Arjona, M. Gutiérrez, 2007, Cancer genetics and cytogenetics.

Molecular analysis of the EGFR gene in astrocytic gliomas: mRNA expression, quantitative‐PCR analysis of non‐homogeneous gene amplification and DNA sequence alterations

M. Alonso, J. Rey, M. Bello, 2005, Neuropathology and applied neurobiology.

Promoter methylation status of multiple genes in brain metastases of solid tumors.

M. Alonso, J. Rey, M. Bello, 2004, International journal of molecular medicine.

Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors.

M. Alonso, J. Rey, M. Bello, 2004, Mutation research.

Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity.

J. Rey, C. Casartelli, M. Gutiérrez, 2009, Cancer genetics and cytogenetics.

DNA methylation of multiple promoter-associated CpG islands in meningiomas: relationship with the allelic status at 1p and 22q

M. Alonso, J. Rey, M. Bello, 2004, Acta Neuropathologica.

Single-Cell Phenotypic Characterization of Human Pituitary GHomas and Non-Functioning Adenomas Based on Hormone Content and Calcium Responses to Hypothalamic Releasing Hormones

J. García-Sancho, L. Senovilla, C. Villalobos, 2015, Front. Oncol..

Multiplex ligation-dependent probe amplification (MLPA) screening in meningioma.

J. Rey, J. Lomas, J. M. de Campos, 2007, Cancer genetics and cytogenetics.

C-band pattern in patients with nervous system tumors.

J. Rey, M. Bello, M. Kusak, 1987, Cancer genetics and cytogenetics.

C-banding studies in lymphocytes from patients with tumors of the nervous system.

J. Rey, J. M. de Campos, J. Benítez, 1985, Cancer genetics and cytogenetics.

Cytogenetic clones in a recurrent neurofibroma.

J. Rey, M. Bello, J. Sarasa, 1987, Cancer genetics and cytogenetics.

Chromosome studies in two human brain tumors.

J. Rey, M. Bello, J. M. de Campos, 1983, Cancer genetics and cytogenetics.

Global Profiling in Vestibular Schwannomas Shows Critical Deregulation of MicroRNAs and Upregulation in Those Included in Chromosomal Region 14q32

B. Meléndez, J. Rey, R. Burbano, 2013, PloS one.

Allelic status of 1p, 14q, and 22q and NF2 gene mutations in sporadic schwannomas.

J. Rey, M. Bello, J. Sarasa, 1998, International journal of molecular medicine.

Meningiomas and schwannomas: molecular subgroup classification found by expression arrays.

J. Rey, C. Casartelli, A. Isla, 2009, International journal of oncology.

Mutational analysis of the DAL-1/4.1B tumour-suppressor gene locus in meningiomas.

J. Rey, M. Bello, A. Isla, 2005, International journal of molecular medicine.

Genomic deletions at 1p and 14q are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not in schwannomas.

J. Rey, C. Casartelli, A. Isla, 2010, Cancer genetics and cytogenetics.

Gene expression analysis of aberrant signaling pathways in meningiomas

B. Meléndez, J. Rey, R. Burbano, 2013, Oncology letters.

Genetic characterization and structural analysis of VHL Spanish families to define genotype–phenotype correlations

M. Urioste, J. Benítez, A. Cebrián, 2004, Human mutation.

Chromosome 22 heterozygosity is retained in most hyperdiploid and pseudodiploid meningiomas.

J. Rey, M. Bello, J. Sarasa, 1993, Cancer genetics and cytogenetics.