المؤلفون: Carla Pollastro, Carmela Ziviello, Valerio Costa, Alfredo Ciccodicola

المصدر: PPAR Research, Vol 2015 (2015)

مصطلحات موضوعية: Biology (General), QH301-705.5

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1687-4757Test; https://doaj.org/toc/1687-4765Test

الوصول الحر: https://doaj.org/article/edef663cc3914c03a3e371b43f630814Test

المؤلفون: Valerio Costa, Antonio Federico, Carla Pollastro, Carmela Ziviello, Simona Cataldi, Pietro Formisano, Alfredo Ciccodicola

المصدر: International Journal of Molecular Sciences, Vol 17, Iss 7, p 1008 (2016)

مصطلحات موضوعية: type 2 diabetes, drug responsiveness, computational predictions, pharmacogenomics, personalized medicine, RNA-sequencing, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

العلاقة: http://www.mdpi.com/1422-0067/17/7/1008Test; https://doaj.org/toc/1422-0067Test

الوصول الحر: https://doaj.org/article/08ec52ff99894952b62a77f9b6ca48d0Test

المؤلفون: Danilo Licastro, Margherita Mutarelli, Ivana Peluso, Kornelia Neveling, Nienke Wieskamp, Rossella Rispoli, Diego Vozzi, Emmanouil Athanasakis, Angela D'Eustacchio, Mariateresa Pizzo, Francesca D'Amico, Carmela Ziviello, Francesca Simonelli, Antonella Fabretto, Hans Scheffer, Paolo Gasparini, Sandro Banfi, Vincenzo Nigro

المصدر: PLoS ONE, Vol 7, Iss 8, p e43799 (2012)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

العلاقة: http://europepmc.org/articles/PMC3430670?pdf=renderTest; https://doaj.org/toc/1932-6203Test

الوصول الحر: https://doaj.org/article/751c2a46e06f4b2ea37e996c6d0f8dffTest

المؤلفون: Francesca Simonelli, Carmela Ziviello, Francesco Testa, Settimio Rossi, Elisa Fazzi, Paolo Emilio Bianchi, Maurizio Fossarello, Sabrina Signorini, Chiara Bertone, Silvana Galantuomo, Francesco Brancati, Alfredo Ciccodicola, Ernesto Rinaldi, Alberto Auricchio, Sandro Banfi

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://iovs.arvojournals.org/pdfaccess.ashx?url%3D/data/journals/iovs/932943/z7g00907004284.pdfTest.

وصف الملف: application/pdf

العلاقة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.1084.2106Test; http://iovs.arvojournals.org/pdfaccess.ashx?url%3D/data/journals/iovs/932943/z7g00907004284.pdfTest

الإتاحة: http://iovs.arvojournals.org/pdfaccess.ashx?url%3D/data/journals/iovs/932943/z7g00907004284.pdfTest

المؤلفون: Romina Sepe, Roberta Esposito, Alfredo Fusco, Alfredo Ciccodicola, Carmela Ziviello, Pierlorenzo Pallante, Valerio Costa, Larissa Valdemarin Bim, Nunzio Antonio Cacciola, Myriam Decaussin-Petrucci

المساهمون: Costa, Valerio, Esposito, Roberta, Ziviello, Carmela, Sepe, Romina, Bim, Larissa Valdemarin, Cacciola, Nunzio Antonio, Decaussin Petrucci, Myriam, Pallante, Pierlorenzo, Fusco, Alfredo, Ciccodicola, Alfredo

المصدر: Oncotarget
Oncotarget 6 (2015): 11242–11251.
info:cnr-pdr/source/autori:Costa V, Esposito R, Ziviello C, Sepe R, Bim LV, Cacciola NA, Decaussin-Petrucci M, Pallante P, Fusco A, Ciccodicola A./titolo:New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma./doi:/rivista:Oncotarget/anno:2015/pagina_da:11242/pagina_a:11251/intervallo_pagine:11242–11251/volume:6
info:cnr-pdr/source/autori:Costa V.; Esposito R.; Ziviello C.; Sepe R.; Bim L.V.; Cacciola N.A.; Decaussin-Petrucci M.; Pallante P.; Fusco A.; Ciccodicola A./titolo:New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma/doi:/rivista:Oncotarget/anno:2015/pagina_da:11242/pagina_a:11251/intervallo_pagine:11242–11251/volume:6
Europe PubMed Central
Scopus-Elsevier
Oncotarget 6 (2015): 11242–11251. doi:10.18632/oncotarget.3593
info:cnr-pdr/source/autori:Costa, Valerio; Esposito, Roberta; Ziviello, Carmela; Sepe, Romina; Bim, Larissa Valdemarin; Cacciola, Nunzio Antonio; Decaussin-Petrucci, Myriam; Pallante, Pierlorenzo; Fusco, Alfredo; Ciccodicola, Alfredo/titolo:New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma/doi:10.18632%2Foncotarget.3593/rivista:Oncotarget/anno:2015/pagina_da:11242/pagina_a:11251/intervallo_pagine:11242–11251/volume:6

مصطلحات موضوعية: endocrine system diseases, DNA Mutational Analysis, medicine.disease_cause, gene fusions, thyroid, Fusion gene, WNK Lysine-Deficient Protein Kinase 1, RNA-sequencing, mutations, papillary carcinomas, Missense mutation, Proto-Oncogene Proteins c-cbl, Receptor, Notch1, Mutation, Intracellular Signaling Peptides and Proteins, Nuclear Proteins, Phenotype, Gene Expression Regulation, Neoplastic, Oncology, Thyroid Cancer, Papillary, N-Acetylgalactosaminyltransferases, Gene Fusion, Research Paper, Mutation, Missense, Biology, Protein Serine-Threonine Kinases, Gene Expression Regulation, Enzymologic, Thyroid carcinoma, Minor Histocompatibility Antigens, Vacuolar Sorting Protein VPS15, Predictive Value of Tests, medicine, Biomarkers, Tumor, Humans, Genetic Predisposition to Disease, Thyroid Neoplasms, Gene, Genetic Association Studies, Neoplasm Staging, Genetic heterogeneity, Carcinoma, DNA Helicases, Cancer, Reproducibility of Results, medicine.disease, Molecular biology, Carcinoma, Papillary, RNA-Sequencing, Case-Control Studies, Cancer research, mutation, papillary carcinoma, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b62fac9c2d8f12e9ecc1140ba54af1fTest
http://europepmc.org/articles/PMC4484453Test

المؤلفون: Alejandro Estrada Cuzcano, Robert K. Koenekoop, Audrey Senechal, Elfride B. W. De Baere, Thomy De Ravel, Sandro Banfi, Susanne Kohl, Carmen Ayuso, Dror Sharon, Carel B. Hoyng, Christian P. Hamel, Bart P. Leroy, Carmela Ziviello, Irma Lopez, Alexandre Bazinet, Bernd Wissinger, Ieva Sliesoraityte, Almudena Avila Fernandez, Karin W. Littink, Sabrina Signorini, Eyal Banin, Liliana Mizrahi Meissonnier, Eberhard Zrenner, Ulrich Kellner, Rob W. J. Collin, Anneke I. Den Hollander, Frans P. M. Cremers, B. Jeroen Klevering, VINGOLO, Enzo Maria

المساهمون: Alejandro Estrada, Cuzcano, Robert K., Koenekoop, Audrey, Senechal, Elfride B. W., De Baere, Thomy De, Ravel, Sandro, Banfi, Susanne, Kohl, Carmen, Ayuso, Dror, Sharon, Carel B., Hoyng, Christian P., Hamel, Bart P., Leroy, Carmela, Ziviello, Irma, Lopez, Alexandre, Bazinet, Bernd, Wissinger, Ieva, Sliesoraityte, Almudena Avila, Fernandez, Karin W., Littink, Vingolo, Enzo Maria, Sabrina, Signorini, Eyal, Banin, Liliana Mizrahi, Meissonnier, Eberhard, Zrenner, Ulrich, Kellner, Rob W. J., Collin, Anneke I., Den Hollander, Frans P. M., Cremer, B., Jeroen Klevering

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23143442; info:eu-repo/semantics/altIdentifier/wos/WOS:000310986700008; volume:130; issue:11; firstpage:1425; lastpage:1432; numberofpages:8; journal:ARCHIVES OF OPHTHALMOLOGY; http://hdl.handle.net/11573/497708Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84867135409

الإتاحة: https://doi.org/10.1001/archophthalmol.2012.2434Test
http://hdl.handle.net/11573/497708Test

المؤلفون: Sandro Banfi, Giovanna Alfano, Marta Lestingi, Diego Circolo, Alfredo Ciccodicola, Ivan Conte, Carmela Ziviello, Anneke I. den Hollander, Cristina Caccioppoli, Mariarosaria Pugliese

المساهمون: Conte, I., Lestingi, M., den Hollander, A., Alfano, G., Ziviello, C., Pugliese, M., Circolo, D., Caccioppoli, C., Ciccodicola, A., Banfi, S., Conte, I, Lestingi, M, den Hollander, A, Alfano, G, Ziviello, C, Pugliese, M, Circolo, D, Caccioppoli, C, Ciccodicola, A, Banfi, Sandro

المصدر: European Journal of Human Genetics, 11, 155-62
European Journal of Human Genetics, 11, 2, pp. 155-62
European journal of human genetics 11 (2003): 155–162. doi:10.1038/sj.ejhg.5200942
info:cnr-pdr/source/autori:Conte I, Lestingi M, den Hollander A, Alfano G, Ziviello C, Pugliese M, Circolo D, Caccioppoli C, Ciccodicola A, Banfi S/titolo:Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerations/doi:10.1038%2Fsj.ejhg.5200942/rivista:European journal of human genetics/anno:2003/pagina_da:155/pagina_a:162/intervallo_pagine:155–162/volume:11

مصطلحات موضوعية: Sequence analysis, Amino Acid Motifs, Molecular Sequence Data, Retinitis, Biology, Retina, Homology (biology), Gene product, Mice, Sequence Analysis, Protein, DC domain, Retinitis pigmentosa, Genetics, medicine, Animals, Neurosensory disorders [UMCN 3.3], Amino Acid Sequence, Eye Proteins, Gene, Genetics (clinical), Animal, Gene Expression Profiling, Retinal Degeneration, Eye Protein, Human diseases, medicine.disease, Molecular biology, RP1, eye diseases, Takifugu, Doublecortin, Gene expression profiling, Gene identification, Genetic defects of metabolism [UMCN 5.1], Organ Specificity, Amino Acid Motif, biology.protein, RP1L1, sense organs

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cd871eff8ef732723ab19db103efd7aTest
https://hdl.handle.net/2066/134338Test

المؤلفون: Antonio Federico, Simona Cataldi, Carla Pollastro, Valerio Costa, Carmela Ziviello, Alfredo Ciccodicola, Pietro Formisano

المساهمون: Costa, Valerio, Federico, Antonio, Pollastro, Carla, Ziviello, Carmela, Cataldi, Simona, Formisano, Pietro, Ciccodicola, Alfredo

المصدر: International Journal of Molecular Sciences, Vol 17, Iss 7, p 1008 (2016)
International Journal of Molecular Sciences
International journal of molecular sciences
17 (2016). doi:10.3390/ijms17071008
info:cnr-pdr/source/autori:Costa V, Federico A, Pollastro C, Ziviello C, Cataldi S, Formisano P, Ciccodicola A./titolo:Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes./doi:10.3390%2Fijms17071008/rivista:International journal of molecular sciences (Print)/anno:2016/pagina_da:/pagina_a:/intervallo_pagine:/volume:17

مصطلحات موضوعية: RNA-sequencing, computational predictions, drug responsiveness, personalized medicine, pharmacogenomics, type 2 diabetes, 0301 basic medicine, pharmacogenomic, In silico, Drug Resistance, computational prediction, Single-nucleotide polymorphism, Locus (genetics), Drug resistance, Regulatory Sequences, Nucleic Acid, Biology, Polymorphism, Single Nucleotide, Catalysis, Receptors, G-Protein-Coupled, lcsh:Chemistry, Inorganic Chemistry, 03 medical and health sciences, Humans, Hypoglycemic Agents, RNA Processing, Post-Transcriptional, Physical and Theoretical Chemistry, lcsh:QH301-705.5, Molecular Biology, Gene, Spectroscopy, Genetic association, Genetics, Calpain, Communication, Organic Chemistry, Intron, General Medicine, Metformin, 3. Good health, Computer Science Applications, Molecular Docking Simulation, drug responsivene, 030104 developmental biology, Diabetes Mellitus, Type 2, lcsh:Biology (General), lcsh:QD1-999, Pharmacogenomics

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::453424a96c435cb50d6b1ee76cf7ab03Test
https://doi.org/10.3390/ijms17071008Test

المؤلفون: Emmanouil Athanasakis, Ivana Peluso, Angela D'Eustacchio, Vincenzo Nigro, Antonella Fabretto, Carmela Ziviello, Nienke Wieskamp, Danilo Licastro, Margherita Mutarelli, Francesca Simonelli, Paolo Gasparini, Rossella Rispoli, F. d’Amico, Kornelia Neveling, Diego Vozzi, Mariateresa Pizzo, Hans Scheffer, Sandro Banfi

المساهمون: Licastro, Danilo, Mutarelli, Margherita, Peluso, Ivana, Neveling, Kornelia, Wieskamp, Nienke, Rispoli, Rossella, Vozzi, Diego, Athanasakis, Emmanouil, D'Eustacchio, Angela, Pizzo, Mariateresa, D'Amico, Francesca, Ziviello, Carmela, Simonelli, Francesca, Fabretto, Antonella, Scheffer, Han, Gasparini, Paolo, Banfi, Sandro, Nigro, Vincenzo, Licastro, D, Mutarelli, M, Peluso, I, Neveling, K, Wieskamp, N, Rispoli, R, Vozzi, D, Athanasakis, E, D'Eustacchio, A, Pizzo, M, D'Amico, F, Ziviello, C, Fabretto, A, Scheffer, H, Gasparini, P

المصدر: PLoS One, 7
PLoS ONE, Vol 7, Iss 8, p e43799 (2012)
PLoS ONE; Vol 7
PLoS ONE
PLoS One, 7, 8

مصطلحات موضوعية: Genetics and Molecular Biology (all), Genetic Screens, Gene Identification and Analysis, lcsh:Medicine, Pilot Projects, Biochemistry, Genome Databases, Exome, Genome Sequencing, lcsh:Science, Child, Exome sequencing, Genetics, 0303 health sciences, Multidisciplinary, Massive parallel sequencing, Genome, Medicine (all), 030305 genetics & heredity, High-Throughput Nucleotide Sequencing, Genomics, 3. Good health, Molecular Diagnostic Techniques, Child, Preschool, Medicine, Usher Syndrome, Genome, Human, Humans, Sequence Analysis, DNA, Usher Syndromes, Agricultural and Biological Sciences (all), Biochemistry, Genetics and Molecular Biology (all), Sequence Analysis, Research Article, Human, Molecular Diagnostic Technique, Sequence Databases, Genetic Counseling, Biology, DNA sequencing, Genomic disorders and inherited multi-system disorders DCN MP - Plasticity and memory [IGMD 3], Genomic disorders and inherited multi-system disorders [IGMD 3], Molecular Genetics, 03 medical and health sciences, Pilot Project, Genetic Testing, Preschool, Genotyping, 030304 developmental biology, Clinical Genetics, lcsh:R, Personalized Medicine, Human Genetics, DNA, Molecular diagnostics, Otorhinolaryngology, Genetics of Disease, Mutation Databases, Human genome, lcsh:Q

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24da4082c71834ce96c610e3d1434943Test
http://hdl.handle.net/2066/108716Test

المؤلفون: Jeannette L. Bennicelli, Carmela Acerra, Sandro Banfi, Settimio Rossi, Carmela Ziviello, Kenneth S. Shindler, T. Michael Redmond, Federico Mingozzi, Kathleen A. Marshall, Francesca Simonelli, Xiaosong Zhu, Enrico Maria Surace, Eric A. Pierce, Katherine A. High, Junwei Sun, Albert M. Maguire, Jennifer Wellman McDonnell, Francesco Testa, J. Fraser Wright, Alberto Auricchio, Gui-Shuang Ying, Jean Bennett

المساهمون: Simonelli, F, Maguire, Am, Testa, F, Pierce, Ea, Mingozzi, F, Bennicelli, Jl, Rossi, S, Marshall, K, Banfi, S, Surace, Enrico Maria, Sun, J, Redmond, Tm, Zhu, X, Shindler, K, Ying, G, Ziviello, C, Acerra, C, Wright, Jf, Mcdonnell, Jw, High, Ka, Bennett, J, Auricchio, Alberto, Simonelli, Francesca, Testa, Francesco, Rossi, Settimio, Banfi, Sandro, Surace, Em, Shindlerks, Auricchio, A.

المصدر: Molecular Therapy
Molecular Therapy; Vol 18

مصطلحات موضوعية: Time Factors, Genetic enhancement, viruses, Leber Congenital Amaurosis, Disease, chemistry.chemical_compound, 0302 clinical medicine, Drug Discovery, Medicine, Vector (molecular biology), Transgenes, Genetics, 0303 health sciences, Dependovirus, 3. Good health, medicine.anatomical_structure, Treatment Outcome, Editorial, Disease Progression, Leber's congenital amaurosis, Molecular Medicine, Adult, cis-trans-Isomerases, Genetic Vectors, Retina, 03 medical and health sciences, Humans, Clinical Trials, Eye Proteins, Molecular Biology, Vision, Ocular, 030304 developmental biology, Pharmacology, Models, Genetic, business.industry, Retinal, Original Articles, Genetic Therapy, medicine.disease, eye diseases, RPE65, chemistry, Cis-trans-Isomerases, Immunology, 030221 ophthalmology & optometry, sense organs, business, Carrier Proteins, Follow-Up Studies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::298c97d708abc418927ba2d6165559edTest
https://pubmed.ncbi.nlm.nih.gov/20195259Test