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Titolo Data di pubblicazione Autore(i) File
Diamond-Blackfan anemia: a congenital defect in erythropoiesis 1996 DIANZANI I; GARELLI E; U. RAMENGHI
Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemia. 1996 Dianzani I; Garelli E; Dompè C; Crescenzio N; Locatelli F; Schilirò G; Castaman G; Bagnara GP; Olivieri NF; Gabutti V; Ramenghi U
Diamond-Blackfan anemia: expansion of erythroid progenitors in vitro by IL-9, but exclusion of a significant pathogenetic role for the IL-9 gene and the hematopoietic gene cluster on chromosome 5q. 1997 DIANZANI I; GARELLI E; CRESCENZIO N; TIMEUS F; MORI PG; VAROTTO S; NOBILI B; BRANDALISE S; OLIVIERI NF; GABUTTI V; U. RAMENGHI
Stem cell factor suppresses apoptosis in neuroblastoma cell lines. 1997 Timeus F; Crescenzio N; Valle P; Pistamiglio P; Piglione M; Garelli E; Ricotti E; Rocchi P; Strippoli P; Cordero di Montezemolo L; Madon E; Ramenghi U; Basso G.
C-KIT IS EXPRESSED IN SOFT TISSUE SARCOMA OF NEUROECTODERMIC ORIGIN AND ITS LIGAND PREVENTS APOPTOSIS OF NEOPLASTIC CELLS 1998 RICOTTI E.; FAGIOLI F.; GARELLI E.; LINARI C.; E. MADON; CRESCENZIO N.; PISTAMIGLIO P.; VAI S.; BERGER M.; CORDERO DI MONTEZEMOLO L.; BASSO G.
Identification of microdeletions spanning the Diamond-Blackfan anemia locus on 19q13 and evidence for genetic heterogeneity. 1998 Gustavsson P; Garelli E; Draptchinskaia N; Ball S; Willig TN; Tentler D; Dianzani I; Punnett HH; Shafer FE; Cario H; Ramenghi U; Glomstein A; Pfeiffer RA; Goringe A; Olivieri NF; Smibert E; Tchernia G; Elinder G; Dahl N
L'anemia di diamond blackfan 1999 Ramenghi U; Garelli E; Dianzani I.
Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression 1999 WILLIG TH; DRAPTCHINSKAIA N; DIANZANI I; BALL S; NIEMEYER C; RAMENGHI U; ORFALI K; GUSTAVSSON P; GARELLI E; A. BRUSCO; TIEMANN C; PERIGNON JL; BOUCHIER C; CICCHIELLO L; DAHL N; MOHANDAS N; TCHERNIA G
Diamond Blackfan anaemia in the Italian population 1999 U. RAMENGHI; GARELLI E.; VALTOLINA S.; CAMPAGNOLI MF.; TIMEUS F.; CRESCENZIO N; MAIR M.; VAROTTO S.; D'AVANZO S.; NOBILI B.; MASSOLO F.; MORI PG.; LOCATELLI F.; GUSTAVSSON P.; DAHL N.; DIANZANI I.
Diamond-Blackfan anemia: report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population. 2000 U. RAMENGHI; CAMPAGNOLI MF; GARELLI E; CARANDO A; BRUSCO A; BAGNARA GP; STRIPPOLI PL; IZZI GC; BRANDALISE S; RICCARDI R; DIANZANI I
Diamond-Blackfan Anemia: an Overview 2000 DIANZANI I; GARELLI E; U. RAMENGHI
Flt-3 and its ligand are expressed in neural crest-derived tumors and promote survival and proliferation of their cell lines. 2001 TIMEUS F; RICOTTI E; CRESCENZIO N; GARELLI E; DORIA A; SPINELLI M; U. RAMENGHI; BASSO G
Rapp-Hodgkin and AEC syndromes due to a new frameshift mutation in the TP63 gene. 2003 Dianzani I; Garelli E; Gustavsson P; Carando A; Gustafsson B; Dahl N; Annerén G.
Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature 2004 CAMPAGNOLI MF; GARELLI E; QUARELLO P; CARANDO A; VAROTTO S; NOBILI B; LONGONI D; PECILE V; ZECCA M; DUFOUR C; RAMENGHI U; DIANZANI I
Anemia di Diamond Blackfan (DBA) : Studio dell’espressione genica. 2004 QUARELLO P; CAMPAGNOLI MF; GARELLI E; CARANDO A; CRESCENZIO N; DORIA A; MARTINO S; RENGA D; U. RAMENGHI; DIANZANI I
Nonsense-mediated and nonstop decay of ribosomal protein S19 mRNA in Diamond-Blackfan anemia 2004 CHATR-ARYAMONTRI A; ANGELINI M; GARELLI E; TCHERNIA G; RAMENGHI U; DIANZANI I; LORENI F
Somatic mosaicism and variable expressivity in Diamond Blackfan anemia (DBA): a gross deletion involving the 19q13 locus in a patient with transient anemia 2005 GARELLI E; QUARELLO P; CAMPAGNOLI MF; BRUSCO A; CARANDO A; MENEGATTI E; CRESCENZIO N; FOGLIA L; DIANZANI I; RAMENGHI U
Interactions between RPS19, mutated in Diamond-Blackfan anemia, and the PIM-1 oncoprotein 2005 CHIOCCHETTI A; GIBELLO L; CARANDO A; ASPESI A; SECCO P; GARELLI E; LORENI F; ANGELINI M; BIAVA A; DAHL N; DIANZANI U; RAMENGHI U; SANTORO C; DIANZANI I
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family 2006 CAMPAGNOLI MF; PUCCI A; GARELLI E; CARANDO A; DEFILIPPI C; LALA R; INGROSSO G; DIANZANI I; FORNI M; RAMENGHI U
The broad spectrum of autoimmune lymphoproliferative disease: molecular bases, clinical features and long-term follow-up in 31 patients 2006 CAMPAGNOLI MF; GARBARINI L; QUARELLO P; GARELLI E; CARANDO A; BARAVALLE V; DORIA A; BIAVA A; CHIOCCHETTI A; ROSOLEN A; DUFOUR C; DIANZANI U; RAMENGHI U
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