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1دورية أكاديمية
المؤلفون: Valli, Roberto, Penzo, Marianna
المساهمون: Valli, Roberto, Penzo, Marianna
مصطلحات موضوعية: ribosome biogenesis, rare disease, ribosomopathy, RPL10, shwachman diamond syndrome, diamond blackfan anaemia, X-linked dyskeratosis congenita, T-ALL leukemia
وصف الملف: ELETTRONICO
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37124624; info:eu-repo/semantics/altIdentifier/wos/WOS:000978836300001; volume:14; firstpage:1; lastpage:3; numberofpages:3; journal:FRONTIERS IN GENETICS; https://hdl.handle.net/11585/922393Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85153527791; https://www.frontiersin.org/articles/10.3389/fgene.2023.1194788/fullTest
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2دورية أكاديمية
المؤلفون: Khalid, Fatima, Phan, Tamara, Qiang, Mingyue, Maity, Pallab, Lasser, Theresa, Wiese, Sebastian, Penzo, Marianna, Alupei, Marius, Orioli, Donata, Scharffetter-Kochanek, Karin, Iben, Sebastian
المساهمون: Khalid, Fatima, Phan, Tamara, Qiang, Mingyue, Maity, Pallab, Lasser, Theresa, Wiese, Sebastian, Penzo, Marianna, Alupei, Mariu, Orioli, Donata, Scharffetter-Kochanek, Karin, Iben, Sebastian
مصطلحات موضوعية: not available
وصف الملف: STAMPA
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36308430; info:eu-repo/semantics/altIdentifier/wos/WOS:000895416000001; volume:32; issue:7; firstpage:1102; lastpage:1113; numberofpages:12; journal:HUMAN MOLECULAR GENETICS; https://hdl.handle.net/11585/921172Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85150665335; https://academic.oup.com/hmg/article/32/7/1102/6779975Test
الإتاحة: https://doi.org/10.1093/hmg/ddac268Test
https://hdl.handle.net/11585/921172Test
https://academic.oup.com/hmg/article/32/7/1102/6779975Test -
3دورية أكاديمية
المؤلفون: Guerrieri, Ania Naila, Bellotti, Chiara, Penzo, Marianna, Columbaro, Marta, Pannella, Micaela, De Vita, Alessandro, Gambarotti, Marco, Mercatali, Laura, Laranga, Roberta, Dozza, Barbara, Vanni, Silvia, Corsini, Serena, Frisoni, Tommaso, Miserocchi, Giacomo, Ibrahim, Toni, Lucarelli, Enrico
المساهمون: Ministero della Salute, Eurovo Group
المصدر: BMC Cancer ; volume 23, issue 1 ; ISSN 1471-2407
مصطلحات موضوعية: Cancer Research, Genetics, Oncology
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4دورية أكاديمية
المؤلفون: Cipolli, Marco, Boni, Christian, Penzo, Marianna, Villa, Isabella, Bolamperti, Simona, Baldisseri, Elena, Frattini, Annalisa, Porta, Giovanni, Api, Martina, Selicato, Nora, Roccia, Pamela, Pollutri, Daniela, Marinelli Busilacchi, Elena, Poloni, Antonella, Caporelli, Nicole, D'Amico, Giovanna, Pegoraro, Anna, Cesaro, Simone, Oyarbide, Usua, Vella, Antonio, Lippi, Giuseppe, Corey, Seth J, Valli, Roberto, Polini, Alessandro, Bezzerri, Valentino
المساهمون: Cipolli, Marco, Boni, Christian, Penzo, Marianna, Villa, Isabella, Bolamperti, Simona, Baldisseri, Elena, Frattini, Annalisa, Porta, Giovanni, Api, Martina, Selicato, Nora, Roccia, Pamela, Pollutri, Daniela, Marinelli Busilacchi, Elena, Poloni, Antonella, Caporelli, Nicole, D'Amico, Giovanna, Pegoraro, Anna, Cesaro, Simone, Oyarbide, Usua, Vella, Antonio, Lippi, Giuseppe, Corey, Seth J, Valli, Roberto, Polini, Alessandro, Bezzerri, Valentino
مصطلحات موضوعية: Shwachman-Diamond syndrome, ataluren, inherited bone marrow failure syndromes, myelodysplastic syndromes
وصف الملف: STAMPA
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37876306; info:eu-repo/semantics/altIdentifier/wos/WOS:001091130500001; volume:204; firstpage:292; lastpage:305; numberofpages:14; journal:BRITISH JOURNAL OF HAEMATOLOGY; https://hdl.handle.net/11562/1110807Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85174577008
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5دورية أكاديمية
المؤلفون: Bacci, Lorenza, Indio, Valentina, Rambaldelli, Guglielmo, Bugarin, Cristina, Magliocchetti, Franco, Del Rio, Alberto, Pollutri, Daniela, Melchionda, Fraia, Pession, Andrea, Lanciotti, Marina, Dufour, Carlo, Gaipa, Giuseppe, Montanaro, Lorenzo, Penzo, Marianna
المساهمون: Bacci, Lorenza, Indio, Valentina, Rambaldelli, Guglielmo, Bugarin, Cristina, Magliocchetti, Franco, Del Rio, Alberto, Pollutri, Daniela, Melchionda, Fraia, Pession, Andrea, Lanciotti, Marina, Dufour, Carlo, Gaipa, Giuseppe, Montanaro, Lorenzo, Penzo, Marianna
مصطلحات موضوعية: Q123R, RPL10 mutation, leukemia, next generation sequencing—NGS, ribosome, translation, uL16 (RPL10)
وصف الملف: ELETTRONICO
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36482893; info:eu-repo/semantics/altIdentifier/wos/WOS:000894482600001; volume:13; firstpage:1; lastpage:11; numberofpages:11; journal:FRONTIERS IN GENETICS; https://hdl.handle.net/11585/909461Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85143348020; https://www.frontiersin.org/articles/10.3389/fgene.2022.1058468/fullTest
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6دورية أكاديمية
المؤلفون: Daniele, Urbani, Penzo, Marianna, Evangelisti, Martina, Parenti, Marco Daniele, Del Rio, Alberto
المصدر: EFSA Supporting Publications ; volume 21, issue 1 ; ISSN 2397-8325 2397-8325
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7دورية أكاديمية
المصدر: Nature Protocols ; ISSN 1754-2189 1750-2799
مصطلحات موضوعية: General Biochemistry, Genetics and Molecular Biology
الإتاحة: https://doi.org/10.1038/s41596-024-00961-9Test
https://www.nature.com/articles/s41596-024-00961-9.pdfTest
https://www.nature.com/articles/s41596-024-00961-9Test -
8دورية أكاديمية
المؤلفون: Verbelen, Benno, Girardi, Tiziana, Sulima, Sergey O., Vereecke, Stijn, Verstraete, Paulien, Verbeeck, Jelle, Royaert, Jonathan, Cinque, Sonia, Montanaro, Lorenzo, Penzo, Marianna, Imbrechts, Maya, Geukens, Nick, Geuens, Thomas, Dierckx, Koen, Pepe, Daniele, Kampen, Kim, De Keersmaecker, Kim
المصدر: Engineering in Life Sciences ; volume 22, issue 2, page 100-114 ; ISSN 1618-0240 1618-2863
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9دورية أكاديمية
المؤلفون: Zacchini, Federico, Venturi, Giulia, De Sanctis, Veronica, Bertorelli, Roberto, Ceccarelli, Claudio, Santini, Donatella, Taffurelli, Mario, Penzo, Marianna, Treré, Davide, Inga, Alberto, Dassi, Erik, Montanaro, Lorenzo
المساهمون: Associazione Italiana per la Ricerca sul Cancro, Roberto and Cornelia Pallotti's Legacy for Cancer Research
المصدر: Genome Biology ; volume 23, issue 1 ; ISSN 1474-760X
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10دورية أكاديمية
المؤلفون: Khalid, Fatima, Phan, Tamara, Qiang, Mingyue, Maity, Pallab, Lasser, Theresa, Wiese, Sebastian, Penzo, Marianna, Alupei, Marius, Orioli, Donata, Scharffetter-Kochanek, Karin, Iben, Sebastian
المساهمون: Deutsche Forschungsgemeinschaft
المصدر: Human Molecular Genetics ; volume 32, issue 7, page 1102-1113 ; ISSN 0964-6906 1460-2083
مصطلحات موضوعية: Genetics (clinical), Genetics, Molecular Biology, General Medicine
الإتاحة: https://doi.org/10.1093/hmg/ddac268Test
https://academic.oup.com/hmg/article-pdf/32/7/1102/49562062/ddac268.pdfTest
