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المؤلفون: Federica Torri, Filippo Spreafico, Daniela Perotti, Beatrice Gamba, Monica Terenziani, Fabio Macciardi, Paolo Radice, Sara Ciceri, Paola Collini
المصدر: Oncotarget
مصطلحات موضوعية: Male, Ribonuclease III, SIX1, 0301 basic medicine, recurrence, Real-Time Polymerase Chain Reaction, Bioinformatics, medicine.disease_cause, Wilms Tumor, 03 medical and health sciences, 0302 clinical medicine, Biomarkers, Tumor, medicine, Humans, SNP, RNA, Messenger, chromosomal anomalies, Child, Survival rate, Drosha, Neoplasm Staging, Chromosome Aberrations, Homeodomain Proteins, Mutation, Reverse Transcriptase Polymerase Chain Reaction, business.industry, High-Throughput Nucleotide Sequencing, Infant, Wilms' tumor, Prognosis, medicine.disease, Kidney Neoplasms, Survival Rate, 030104 developmental biology, Oncology, Chromosome 3, Chromosomes, Human, Pair 1, miRNA processor genes, Tumor progression, Child, Preschool, 030220 oncology & carcinogenesis, Genomic Profile, Female, Chromosomes, Human, Pair 3, Neoplasm Recurrence, Local, business, Chromosomes, Human, Pair 16, Research Paper
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0173da4ef826848de883a6c2e5ae91d9
https://doi.org/10.18632/oncotarget.6950 -
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المؤلفون: Paolo Radice, Filippo Spreafico, Daniela Perotti, Maura Massimino, Beatrice Gamba, Richard Fabian Schumacher, Silvia Fasoli, Paola Collini, Monica Terenziani, Bercich Luisa, Fulvio Porta, Gianfranco Savoldi, Lucio Giordano, Lucia Dora Notarangelo
المصدر: American Journal of Medical Genetics Part A. 155:1419-1424
مصطلحات موضوعية: medicine.medical_specialty, Pathology, DNA Mutational Analysis, Molecular Sequence Data, Loss of Heterozygosity, medicine.disease_cause, Wilms Tumor, Germline, Loss of heterozygosity, Tuberous sclerosis, Tuberous Sclerosis, Internal medicine, Tuberous Sclerosis Complex 2 Protein, Genetics, medicine, Humans, Allele, WT1 Proteins, Genetics (clinical), X chromosome, Sequence Deletion, Mutation, Base Sequence, business.industry, Tumor Suppressor Proteins, Histological Techniques, Wilms' tumor, medicine.disease, Phenotype, Endocrinology, Child, Preschool, Female, TSC2, business
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المؤلفون: Monica Miozzo, Clelia Tiziana Storlazzi, Paola Collini, Luciana Impera, Massimo Carella, Beatrice Gamba, Daniela Perotti, Savino Calvano, Filippo Spreafico, Orazio Palumbo, Paolo Radice, Leopoldo Zelante, Lucia Miglionico, Giulia Sindici, Silvia Tabano
المصدر: American Journal of Medical Genetics Part A. :1756-1763
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, DNA Copy Number Variations, Genotype, Ring chromosome, Biology, Wilms Tumor, Young Adult, Pregnancy, Chromosome regions, Gene duplication, Genetics, medicine, Humans, Ring Chromosomes, Promoter Regions, Genetic, In Situ Hybridization, Fluorescence, Genetics (clinical), Comparative Genomic Hybridization, Mosaicism, Chromosomes, Human, Pair 11, Infant, Newborn, Cytogenetics, Infant, Cancer, Chromosome, Wilms' tumor, DNA Methylation, medicine.disease, Molecular biology, Child, Preschool, Karyotyping, Cytogenetic Analysis, Leukocytes, Mononuclear, Female, Comparative genomic hybridization
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المؤلفون: Filippo Spreafico, Beatrice Gamba, Paolo Radice, Franca Fossati-Bellani, Maria Adele Testi, Daniela Perotti, Michele Sardella, Fausto Fedeli, Monica Terenziani, Gianluigi Ardissino
المصدر: Pediatric Nephrology. 24:1413-1417
مصطلحات موضوعية: Male, Pathology, medicine.medical_specialty, Genes, Wilms Tumor, DNA Mutational Analysis, Nonsense mutation, Nystagmus, urologic and male genital diseases, Wilms Tumor, Germline, Nephropathy, Exon, Cryptorchidism, medicine, Humans, Sex organ, Base Sequence, urogenital system, Genitourinary system, business.industry, Infant, Newborn, Infant, Wilms' tumor, medicine.disease, female genital diseases and pregnancy complications, Codon, Nonsense, Nephrology, Child, Preschool, Pediatrics, Perinatology and Child Health, medicine.symptom, business, Nystagmus, Congenital
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المؤلفون: Paolo Radice, Serena Catania, Marilina Nantron, Paolo Verderio, Andrea Pession, Pio D'Adamo, Fabio Macciardi, Filippo Spreafico, Paolo Indolfi, Franca Fossati-Bellani, Maurizio Bianchi, Paola Collini, Federica Torri, Beatrice Gamba, Daniela Perotti, Monica Terenziani, Sara Pizzamiglio, Paolo D'Angelo
المساهمون: Perotti D, Spreafico F, Torri F, Gamba B, D'Adamo P, Pizzamiglio S, Terenziani M, Catania S, Collini P, Nantron M, Pession A, Bianchi M, Indolfi P, D'Angelo P, Fossati-Bellani F, Verderio P, Macciardi F, Radice P, Daniela, Perotti, Filippo, Spreafico, Federica, Torri, Beatrice, Gamba, D'Adamo, ADAMO PIO, Sara, Pizzamiglio, Monica, Terenziani, Serena, Catania, Paola, Collini, Marilina, Nantron, Andrea, Pession, Maurizio, Bianchi, Paolo, Indolfi, Paolo, D'Angelo, Franca Fossati, Bellani, Paolo, Verderio, Fabio, Macciardi, Paolo, Radice
المصدر: Genes, Chromosomes and Cancer; Vol 51
مصطلحات موضوعية: Oncology, Genetic Markers, Male, Cancer Research, medicine.medical_specialty, Adolescent, DNA Copy Number Variations, Single-nucleotide polymorphism, Kaplan-Meier Estimate, Biology, Allelic Imbalance, Bioinformatics, Polymorphism, Single Nucleotide, Wilms Tumor, 03 medical and health sciences, 0302 clinical medicine, genetic [DNA Copy Number Variations], Recurrence, Internal medicine, Genetics, medicine, SNP, Humans, Genetic Predisposition to Disease, DNA Copy Number Variations: genetics, Prospective Studies, Allele, Child, Survival rate, Genotyping, 030304 developmental biology, Chromosome Aberrations, 0303 health sciences, Genome, Human, Chromosome, Infant, Wilms' tumor, medicine.disease, ADVERSE PROGNOSTIC-FACTOR, CANCER-STUDY-GROUP, CHILDRENS-CANCER, INTERNATIONAL-SOCIETY, EXPRESSION PATTERNS, RENAL TUMORS, ALLELE LOSS, STAGE-I, HETEROZYGOSITY, 16Q, 3. Good health, Genetic marker, 030220 oncology & carcinogenesis, Child, Preschool, Female, Genome-Wide Association Study
وصف الملف: STAMPA
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae91197928ea3017decfe9fd46c441b0
http://hdl.handle.net/11368/2594021 -
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المؤلفون: Andrea Pession, Monica Terenziani, Franca Fossati-Bellani, Paolo Radice, Michele Sardella, Filippo Spreafico, Beatrice Gamba, Daniela Perotti, Paola Collini, Marilina Nantron
المساهمون: Perotti D, Gamba B, Sardella M, Spreafico F, Terenziani M, Collini P, Pession A, Nantron M, Fossati-Bellani F, Radice P.
المصدر: Oncogene. 27(33)
مصطلحات موضوعية: Male, Cancer Research, DNA Mutational Analysis, Loss of Heterozygosity, Biology, medicine.disease_cause, Wilms Tumor, Loss of heterozygosity, Germline mutation, Genetics, medicine, Humans, Allele, Molecular Biology, X chromosome, Alleles, Adaptor Proteins, Signal Transducing, Mutation, Chromosomes, Human, X, Tumor Suppressor Proteins, Chromosome, Wilms' tumor, medicine.disease, Female, Carcinogenesis, Gene Deletion, Microsatellite Repeats
وصف الملف: STAMPA
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المؤلفون: Edoardo Marchesi, Paolo Radice, Marilina Nantron, Beatrice Gamba, Daniela Perotti, Filippo Spreafico, Maurizio Bianchi, Antonio Fiorino, Silvana Canevari, Paola Collini, Andrea Pession, Loris De Cecco
المصدر: Cancer Research. 75:3268-3268
مصطلحات موضوعية: Oncology, Cancer Research, medicine.medical_specialty, Wilms' tumor, Disease, Gene signature, Biology, Malignancy, medicine.disease, Phenotype, Primary tumor, Internal medicine, Immunology, Gene expression, medicine, Gene
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::53e80eac1bc9ac14248c940694aad131
https://doi.org/10.1158/1538-7445.am2015-3268 -
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المؤلفون: Beatrice Gamba, Gabriele Bucci, Giacomo Manenti, Antonio Fiorino, Paolo Radice, Daniela Perotti
المصدر: Cancer Research. 72:1423-1423
مصطلحات موضوعية: Cell fate commitment, Genetics, Cancer Research, Oncology, POU domain, GATA2, HEK 293 cells, Kidney development, MEF2C, Biology, Gene, Transcription factor
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::5b51a6a5a616534e17dfb38f2714eb36
https://doi.org/10.1158/1538-7445.am2012-1423 -
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المؤلفون: Paolo Radice, Paola Collini, Maurizio Bianchi, Paola Corbetta, Daniela Perotti, Fraia Melchionda, Monica Terenziani, P. Mondini, Serena Catania, Marilina Nantron, Filippo Spreafico, Federica Torri, Fabio Macciardi, Sara Ciceri, Beatrice Gamba, Martina Di Martino, Andrea Di Cataldo, Paolo D'Angelo
المصدر: Scopus-Elsevier
Oncotargetمصطلحات موضوعية: 0301 basic medicine, Genetics, Wilms tumor, Wilms' tumor, Single-nucleotide polymorphism, Biology, medicine.disease, CHEK2, SNP array, Oncology, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, CDKN2A, 030220 oncology & carcinogenesis, RNA splicing, medicine, Missense mutation, Epigenetics, Gene, Research Paper
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d55c64abc193a63d9d41463dadf704f5
http://www.scopus.com/inward/record.url?eid=2-s2.0-85053909091&partnerID=MN8TOARS