DE MARCHI, Mario

DE MARCHI, Mario  

SCIENZE MEDICHE  

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Risultati 1 - 20 di 180 (tempo di esecuzione: 0.008 secondi).
Titolo Data di pubblicazione Autore(i) File
A Bg/II polymorphism in the COL4A6 gene. 1994 RENIERI A ;GALLI L ;ZHOU J ;BALLABIO A ;DE MARCHI M
A case of Klinefelter's syndrome with 47, Xi(Xq)Y karyotype 1980 Ponzio G; DeMarchi M; Gallone G; Fonzo D; Carbonara AO
[A case of pericentric inversion of chromosome 5 in a subject with papillary carcinoma of the thyroid and primary amenorrhea] 1986 PONZIO G ;ISAIA GC ;MUSSETTA M ;SAVIN E ;DE MARCHI M ;CARBONARA A
A new case of gamma-heavy chain disease (LIA protein) with deletion of the hinge region. 1984 SANTORO C ;DE MARCHI M ;VAN LOGHEM E ;DE LANGE G ;MALFI G ;VITELLI A ;CARBONARA AO
A new restriction fragment length polymorphism in the haptoglobin gene region 1985 S. Oliviero; M. De Marchi; G. Bensi; G. Raugei and A.O.Carbonara
[A new test (conglutinin solid phase with anti IgA) for the detection of serum immune complexes in IgA antibody components] 1980 COPPO R ;DE MARCHI M ;CARBONARA AO ;BOCCAZZI C ;BULZOMI MR ;MESSINA M ;MARTINA G ;ROLLINO C ;SEGOLONI G ;ROCCATELLO D ;PICCOLI G
A new test for IgA containing immune complexes or aggregated IgA: its application to Berger and Schönlein-Henoch nephritis. 1980 COPPO R ;DE MARCHI M ;APRATO A ;ROCCATELLO D ;MESSINA M ;SEGOLONI G ;CAMUSSI G ;ALLOATTI S ;GIACCHINO F ;CARBONARA AO ;VERCELLONE A ;PICCOLI G
A non-redundant ATM-, NBS1-, and p53-dependent apoptotic pathway induced by unrepaired double-strand breaks in human T lymphocytes 2007 Turinetto V; Porcedda P; Lantelme E; De Marchi M; Amoroso A; Giachino C
A novel defect in mitochondrial p53 accumulation following DNA damage confers apoptosis resistance in Ataxia Telangiectasia and Nijmegen Breakage Syndrome T cells 2009 V Turinetto; P Porcedda; E Lantelme; L Orlando; L Accomasso; V Minieri; M De Marchi; A Amoroso; D Delia; C Giachino
A novel defect in mitochondrial p53 accumulation following DNA damage confers apoptosis resistance in Ataxia Telangiectasia and Nijmegen Breakage Syndrome T-cells 2010 Turinetto, Valentina; Porcedda, P; Orlando, Luca; Lantelme, Erica Maria; Accomasso, Lisa; Minieri, Valentina; Amoroso, Antonio; DE MARCHI, Mario; Delia, D; Giachino, Claudia
A novel defect in mitochondrial p53 accumulation following DNA damage confers apoptosis resistance in Ataxia Telangiectasia and Nijmegen Breakage Syndrome T-cells 2010 Turinetto, Valentina; Porcedda, P; Minieri, Valentina; Orlando, Luca; Lantelme, Erica Maria; Accomasso, Lisa; Amoroso, Antonio; DE MARCHI, Mario; Zannini, L; Delia, D; Giachino, Claudia
A novel frameshift deletion in type IV collagen alpha 5 gene in a juvenile-type Alport syndrome patient: an adenine deletion (2940/2943 del A) in exon 34 of COL4A5. 1994 PEISSEL B ;ROSSETTI S ;RENIERI A ;GALLI L ;DE MARCHI M ;BATTINI G ;MERONI M ;SESSA A ;SCHIAVANO S ;PIGNATTI PF
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome. 1995 TURCO AE ;ROSSETTI S ;BIASI MO ;RIZZONI G ;MASSELLA L ;SAARINEN NH ;RENIERI A ;PIGNATTI PF ;DE MARCHI M
A radioimmunoassay typing study of non-DQw2-associated celiac disease. 1986 TOSI R ;TANIGAKI N ;POLANCO I ;DE MARCHI M ;WOODROW JC ;HETZEL PA
A rapid flow cytometry test based on histone H2AX phosphorylation for the sensitive and specific diagnosis of Ataxia Telangiectasia 2007 Giachino C; Turinetto V; Cavalieri S; Lantelme E; Orlando L; Ricardi U; De Marchi M; Amoroso A; Gregori D; Porcedda P
A recurrent breakpoint in the most common deletion of the Ig heavy chain locus (delA1-GP-G2-G4-E) 1999 BRUSCO A.; SAVIOZZI S.; CINQUE F.; BOTTARO A.; M. DE MARCHI
A simple method for sodium dodecyl-sulfate-polyacrylamide gel electrophoresis analysis of monoclonal components. 1981 SANTORO C ;DE MARCHI M ;CARBONARA AO
Activation of human mature T lymphocytes through TCR engagement in the presence of IL-7 can induce receptor revision 2004 Lantelme E.; Mantovani S.; Turinetto V.; Porcedda P.; De Marchi M.; Giachino C.
Allogeneic antibodies detected by inhibition of lymphocyte reactivity and by immunofluorescence. 1973 CARBONARA AO ;DE MARCHI M ;TRINCHIERI G ;VARETTO O ;CURTONI ES ;CEPPELLINI R
Alport syndrome caused by a 5' deletion within the COL4A5 gene. 1992 RENIERI A ;SERI M ;MYERS JC ;PIHLAJANIEMI T ;SESSA A ;RIZZONI G ;DE MARCHI M