Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Elisa Pavesi"'
Publikováno v:
Water, Vol 13, Iss 2, p 153 (2021)
Time-dependent rheological properties and thixotropy of reconstituted debris-flows samples taken from channel bank deposits are examined using a commercial rheometer equipped with a vane rotor geometric system. Sweep tests and creep tests were carrie
Externí odkaz:
https://doaj.org/article/37923acee1334df3aa1a88f3d64afb32
Autor:
Serena Macrì, Elisa Pavesi, Rossella Crescitelli, Anna Aspesi, Claudia Vizziello, Carlotta Botto, Paola Corti, Paola Quarello, Patrizia Notari, Ugo Ramenghi, Steven Robert Ellis, Irma Dianzani
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0138200 (2015)
Diamond-Blackfan Anaemia (DBA) is a rare inherited anaemia caused by heterozygous mutations in one of 13 ribosomal protein genes. Erythroid progenitors (BFU-E and CFU-E) in bone marrow (BM) show a proapoptotic phenotype. Suspicion of DBA is reached a
Externí odkaz:
https://doaj.org/article/a1c3e6f53aa74e10a720cd0223b55a8a
Autor:
Irma Dianzani, Adriana Carando, Ugo Ramenghi, Paola Quarello, Sara Parrella, Emanuela Garelli, Elisa Pavesi, Steven R. Ellis, Margherita Nardi, Anna Aspesi
Publikováno v:
Pediatric Blood & Cancer. 61:1319-1321
Mutations in the hematopoietic transcription factor GATA-1 alter the proliferation/differentiation of hemopoietic progenitors. Mutations in exon 2 interfere with the synthesis of the full-length isoform of GATA-1 and lead to the production of a short
Autor:
Elisa Pavesi, Steven R. Ellis, Irma Dianzani, Paola Quarello, Anna Aspesi, Serena Macrì, Rossella Crescitelli, Paola Corti, Claudia Vizziello, Patrizia Notari, Ugo Ramenghi, Carlotta Botto
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0138200 (2015)
PLoS ONE
PLoS ONE
Diamond-Blackfan Anaemia (DBA) is a rare inherited anaemia caused by heterozygous mutations in one of 13 ribosomal protein genes. Erythroid progenitors (BFU-E and CFU-E) in bone marrow (BM) show a proapoptotic phenotype. Suspicion of DBA is reached a
Autor:
Irma Dianzani, Rossella Crescitelli, Antonella Ronchi, Elisa Robotti, Stefano Gustincich, Lydie Da Costa, Elisa Pavesi, Emilio Marengo, Hélène Moniz, Paola Roncaglia, Anna Aspesi, Claudio Santoro, Narla Mohandas, Steven R. Ellis, Simone Merlin, Ugo Ramenghi, Ilenia Boria, Antonia Follenzi, Federica Avondo
Publikováno v:
Gene
Defects in genes encoding ribosomal proteins cause Diamond Blackfan Anemia (DBA), a red cell aplasia often associated with physical abnormalities. Other bone marrow failure syndromes have been attributed to defects in ribosomal components but the lin
Autor:
Irma Dianzani, Margherita Ruoppolo, Laura Ingenito, Marianna Caterino, Esther Imperlini, Claudio Santoro, Anna Aspesi, Daniela Pagnozzi, Elisa Pavesi
Publikováno v:
Proteomics. 14(20)
Diamond-Blackfan anemia, characterized by defective erythroid progenitor maturation, is caused in one-fourth of cases by mutations of ribosomal protein S19 (RPS19), which is a component of the ribosomal 40S subunit. Our previous work described protei
Autor:
Anna Aspesi, Margherita Ruoppolo, Irma Dianzani, Fabrizio Loreni, Marianna Caterino, Marta Armiraglio, Elisa Pavesi, Claudia Corbo, Esther Imperlini
The biochemical phenotype of cells affected by ribosomal stress has not yet been studied in detail. Here we report a comparative proteomic analysis of cell lines silenced for the RPS19 gene versus cell lines transfected with scramble shRNA cells perf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55d0827cab52e83dc014467b04a10bd1
https://hdl.handle.net/11588/567292
https://hdl.handle.net/11588/567292
Autor:
Mutlu Kartal, Maud Simansour, Adrianna Vlachos, Ilenia Boria, Emanuela Garelli, Catherine Clinton, Irma Dianzani, Thierry Leblanc, Hanna T. Gazda, Niklas Dahl, Michael Landowski, Mee Rie Sheen, Ugo Ramenghi, Christopher Buros, Eva Atsidaftos, Alan H. Beggs, Anna Aspesi, Lori J. Dobson, Elisa Pavesi, Alexis Proust, Lydie Da Costa, Paola Quarello, Dagmar Pospisilova, Steven R. Ellis, Jeffrey M. Lipton, Joerg J Meerpohl, Daniela Ferrante, Anne-Sophie Fröjmark, Radek Cmejla
Publikováno v:
Human Mutation
Human Mutation, Wiley, 2010, 31 (12), pp.1269. ⟨10.1002/humu.21383⟩
Human Mutation, Wiley, 2010, 31 (12), pp.1269. ⟨10.1002/humu.21383⟩
International audience; Diamond-Blackfan Anemia (DBA) is characterized by a defect in erythroid progenitor differentation and, clinically, by anemia and malformations. DBA exhibits an autosomal dominant pattern of inheritance with incomplete penetran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3965492fbf71a9956c15e4090e655ee2
https://europepmc.org/articles/PMC4485435/
https://europepmc.org/articles/PMC4485435/
Autor:
Anna Aspesi, Elisa Pavesi, Stefano Vallero, Alberto Rocci, Marina Lanciotti, Ugo Ramenghi, Irma Dianzani
Publikováno v:
Pediatric bloodcancer. 55(3)
Dyskeratosis congenita (DC) is a genetically heterogeneous syndrome characterized by reticular skin pigmentation, nail dystrophy, mucosal leukoplakia, short telomeres, and a predisposition to bone marrow failure and malignancy. Patients carrying muta
Autor:
Marina Lanciotti, Marco Risso, A. P. Iori, Irma Dianzani, Ugo Ramenghi, Giuseppe Santamaria, Marta Pillon, Carlo Dufour, Daniela Longoni, Simona Pigullo, Maria Teresa Van Lint, Johanna Svahn, Elisa Pavesi
Background Telomerase complex genes mutations (DKC1, TERC, TERT, and NOP10) lead to premature telomere shortening and are responsible for different forms of dyskeratosis congenita. TERC and TERT mutations were also found in patients with aplastic ane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b6bcce8ad9f4838f30ec4c2b7ff85cd
http://hdl.handle.net/2318/63242
http://hdl.handle.net/2318/63242