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1دورية أكاديميةGround deformation reveals the scale-invariant conduit dynamics driving explosive basaltic eruptions
المؤلفون: M. Ripepe, G. Lacanna, M. Pistolesi, M. C. Silengo, A. Aiuppa, M. Laiolo, F. Massimetti, L. Innocenti, M. Della Schiava, M. Bitetto, F. P. La Monica, T. Nishimura, M. Rosi, D. Mangione, A. Ricciardi, R. Genco, D. Coppola, E. Marchetti, D. Delle Donne
المصدر: Nature Communications, Vol 12, Iss 1, Pp 1-8 (2021)
مصطلحات موضوعية: Science
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2041-1723
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2دورية أكاديمية
المؤلفون: E. Marchetti, A. van Herwijnen, M. Christen, M. C. Silengo, G. Barfucci
المصدر: Earth Surface Dynamics, Vol 8, Pp 399-411 (2020)
مصطلحات موضوعية: Dynamic and structural geology, QE500-639.5
وصف الملف: electronic resource
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المؤلفون: A, Mussa, S, Russo, A, de Crescenzo, A, Freschi, L, Calzari, S, Maitz, M, Macchiaiolo, C, Molinatto, G, Baldassarre, M, Mariani, L, Tarani, M F, Bedeschi, D, Milani, D, Melis, A, Bartuli, M V, Cubellis, A, Selicorni, M C, Silengo, L, Larizza, A, Riccio, G B, Ferrero
المساهمون: Mussa, A, Russo, S, de Crescenzo, A, Freschi, A, Calzari, L, Maitz, S, Macchiaiolo, M, Molinatto, C, Baldassarre, G, Mariani, M, Tarani, L, Bedeschi, M. F, Milani, D, Melis, D, Bartuli, A, Cubellis, MARIA VITTORIA, Selicorni, A, Silengo, M. C, Larizza, L, Riccio, A, Ferrero, G. B., Russo, S., de Crescenzo, A., Freschi, A., Calzari, L., Maitz, S., Macchiaiolo, M., Molinatto, C., Baldassarre, G., Mariani, M., Tarani, L., Bedeschi, M. F., Milani, D., Melis, D., Bartuli, A., Cubellis, M. V., Selicorni, A., Silengo, M. C., Larizza, L., Riccio, Andrea
المصدر: Clinical genetics 90 (2016): 21–27. doi:10.1111/cge.12759
info:cnr-pdr/source/autori:Mussa, A.; Russo, S.; de Crescenzo, A.; Freschi, A.; Calzari, L.; Maitz, S.; Macchiaiolo, M.; Molinatto, C.; Baldassarre, G.; Mariani, M.; Tarani, L.; Bedeschi, M. F.; Milani, D.; Melis, D.; Bartuli, A.; Cubellis, M. V.; Selicorni, A.; Silengo, M. C.; Larizza, L.; Riccio, A.; Ferrero, G. B./titolo:Fetal growth patterns in Beckwith-Wiedemann syndrome/doi:10.1111%2Fcge.12759/rivista:Clinical genetics/anno:2016/pagina_da:21/pagina_a:27/intervallo_pagine:21–27/volume:90مصطلحات موضوعية: Beckwith-Wiedemann Syndrome, phenotype, genotype, Beckwith–Wiedemann, Gene Expression, Gestational Age, fetal growth, overgrowth, Anthropometry, Chromosomes, Human, Pair 11, Cyclin-Dependent Kinase Inhibitor p57, Fetal Development, Fetus, Genotype, Humans, Infant, Newborn, Mutation, Phenotype, Premature Birth, DNA Methylation, Genomic Imprinting, Uniparental Disomy, Chromosomes, Beckwith-Wiedemann, Fetal growth, Overgrowth, Genetics (clinical), Genetics, Pair 11, Infant, Newborn, Human
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6af8394faf64ca02aff665df96205ba2
http://hdl.handle.net/11588/667487 -
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المصدر: Open Geosciences, Vol 7, Iss 1 (2015)
مصطلحات موضوعية: QE1-996.5, Seismic microzonation, hvsr, General Earth and Planetary Sciences, site effect, Geology, Environmental Science (miscellaneous), microzonation, microtremors, Seismology
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المؤلفون: P, Makrythanasis, B W, van Bon, M, Steehouwer, B, Rodríguez-Santiago, M, Simpson, P, Dias, B M, Anderlid, P, Arts, M, Bhat, B, Augello, E, Biamino, E M H F, Bongers, M, Del Campo, I, Cordeiro, A M, Cueto-González, I, Cuscó, C, Deshpande, E, Frysira, L, Izatt, R, Flores, E, Galán, B, Gener, C, Gilissen, S M, Granneman, J, Hoyer, H G, Yntema, C M, Kets, D A, Koolen, C l, Marcelis, A, Medeira, L, Micale, S, Mohammed, S A, de Munnik, A, Nordgren, S, Psoni, W, Reardon, N, Revencu, T, Roscioli, M, Ruiterkamp-Versteeg, H G, Santos, J, Schoumans, J H M, Schuurs-Hoeijmakers, M C, Silengo, L, Toledo, T, Vendrell, I, van der Burgt, B, van Lier, C, Zweier, A, Reymond, R C, Trembath, L, Perez-Jurado, J, Dupont, B B A, de Vries, H G, Brunner, J A, Veltman, G, Merla, S E, Antonarakis, A, Hoischen
المصدر: Clinical Genetics, Vol. 84, No 6 (2013) pp. 539-545
مصطلحات موضوعية: Male, Kabuki syndrome, Facies, Niikawa–Kuroki syndrome, Sequence Analysis, DNA, genotype–phenotype correlation, Hematologic Diseases, Neoplasm Proteins, DNA-Binding Proteins, Phenotype, Vestibular Diseases, Face, Mutation, MLL2, Humans, ddc:576.5, Abnormalities, Multiple, Female, Genetic Association Studies
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المؤلفون: P, Franceschini, M C, Silengo, G F, Davi, M A, Santoro, G, Prandi, C, Fabris
المصدر: Human genetics. 44(3)
مصطلحات موضوعية: Chromosomes, Human, 6-12 and X, Phenotype, Infant, Newborn, Humans, Abnormalities, Multiple, Female, Chromosome Deletion, Translocation, Genetic
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المؤلفون: Giuseppina Baldassarre, Luigi Tarani, Agostina De Crescenzo, Maria Vittoria Cubellis, Silvia Maitz, Maria Francesca Bedeschi, Margherita Silengo, Andrea Freschi, Marina Macchiaiolo, Cristina Molinatto, Silvia Russo, Donatella Milani, Luciano Calzari, Andrea Riccio, Milena Mariani, Giovanni Battista Ferrero, Andrea Bartuli, Lidia Larizza, Daniela Melis, Angelo Selicorni, Alessandro Mussa
المساهمون: A., Mussa, S., Russo, A. D., Crescenzo, A., Freschi, L., Calzari, S., Maitz, M., Macchiaiolo, C., Molinatto, G., Baldassarre, M., Mariani, L., Tarani, M. F., Bedeschi, D., Milani, D., Meli, A., Bartuli, Cubellis, MARIA VITTORIA, A., Selicorni, M. C., Silengo, L., Larizza, A., Riccio, G. B., Ferrero, Mussa, Alessandro, Russo, Silvia, de Crescenzo, Agostina, Freschi, Andrea, Calzari, Luciano, Maitz, Silvia, Macchiaiolo, Marina, Molinatto, Cristina, Baldassarre, Giuseppina, Mariani, Milena, Tarani, Luigi, Bedeschi, Maria Francesca, Milani, Donatella, Melis, Daniela, Bartuli, Andrea, Cubellis, Maria Vittoria, Selicorni, Angelo, Cirillo Silengo, Margherita, Larizza, Lidia, Riccio, Andrea, Ferrero, Giovanni Battista
المصدر: European journal of human genetics (Online) (2015). doi:10.1038/ejhg.2015.88
info:cnr-pdr/source/autori:Mussa A.; Russo S.; de Crescenzo A.; Freschi A.; Calzari L.; Maitz S.; Macchiaiolo M.; Molinatto C.; Baldassarre G.; Mariani M.; Tarani L.; Bedeschi M.F.; Milani D.; Melis D.; Bartuli A.; Cubellis M.V.; Selicorni A.; Cirillo Silengo M.; Larizza L.; Riccio A.; Ferrero G.B./titolo:(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome/doi:10.1038%2Fejhg.2015.88/rivista:European journal of human genetics (Online)/anno:2015/pagina_da:/pagina_a:/intervallo_pagine:/volumeمصطلحات موضوعية: Male, 0301 basic medicine, Hepatoblastoma, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Beckwith-Wiedemann Syndrome, Genotype, Beckwith–Wiedemann syndrome, genotype-phenotype correlation, 030105 genetics & heredity, Biology, Gastroenterology, Article, Chromosomes, Organomegaly, Genomic Imprinting, 03 medical and health sciences, paternal uniparental disonomy, assisted reproductive technology, Neoplasms, Internal medicine, Genetics, medicine, Macroglossia, Humans, Pair 11, Cyclin-Dependent Kinase Inhibitor p57, Genetic Association Studies, Genetics (clinical), Chromosomes, Human, Pair 11, Cytogenetics, DNA Methylation, Female, Phenotype, medicine.disease, Chromosomal region, Nevus flammeus, medicine.symptom, Human
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::077edba535dc3707e8803d0aa1796385
http://hdl.handle.net/11588/608470 -
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المؤلفون: Cecilia Anichini, Katrin Rademacher, Flavia Cerrato, Jasmin Beygo, Margherita Silengo, Andrea Riccio, Bernhard Horsthemke, Thorsten Enklaar, Karin Buiting, Angela Sparago, Maria Vittoria Cubellis, Andrea Guala, Dirk Prawitt, Notker Graf, Agostina De Crescenzo, Valentina Citro, Melanie Heitmann
المساهمون: Beygo, J, Citro, V, Sparago, A, De Crescenzo, A, Cerrato, Flavia, Heitmann, M, Rademacher, K, Guala, A, Enklaar T., Anichini C, Cirillo Silengo, M, Graf, N, Prawitt, D, Cubellis, Mv, Horstemke, B, Buiting, K, Riccio, Andrea, J., Beygo, V., Citro, A., Sparago, A., De Crescenzo, F., Cerrato, M., Heitmann, K., Rademacher, A., Guala, T., Enklaar, C., Anichini, M. C., Silengo, N., Graf, D., Prawitt, Cubellis, MARIA VITTORIA, B., Horstemke, K., Buiting, A., Riccio
المصدر: Human molecular genetics
22(3) (2013): 544–557. doi:10.1093/hmg/dds465
info:cnr-pdr/source/autori:Beygo J, Citro V, Sparago A, De Crescenzo A, Cerrato F, Heitmann M, Rademacher K, Guala A, Enklaar T, Anichini C, Cirillo Silengo M, Graf N, Prawitt D, Cubellis MV, Horsthemke B, Buiting K, Riccio A./titolo:The molecular function and clinical phenotype of partial deletions of the IGF2%2FH19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites/doi:10.1093%2Fhmg%2Fdds465/rivista:Human molecular genetics (Print)/anno:2013/pagina_da:544/pagina_a:557/intervallo_pagine:544–557/volume:22(3)
Human Molecular Geneticsمصطلحات موضوعية: CCCTC-Binding Factor, Chromatin Immunoprecipitation, Medizin, Biology, Genomic Imprinting, Insulin-Like Growth Factor II, Genetics, Humans, Gene Silencing, Allele, Enhancer, Molecular Biology, Gene, Genetics (clinical), Alleles, Cells, Cultured, Binding Sites, Chromosomes, Human, Pair 11, General Medicine, Methylation, Sequence Analysis, DNA, Articles, DNA Methylation, Penetrance, Phenotype, Pedigree, Repressor Proteins, Gene Expression Regulation, CTCF, Genetic Loci, DNA methylation, RNA, Long Noncoding, Gene Deletion
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc68c41f6160eb6b91717145212bb5fa
http://hdl.handle.net/11591/187142
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