THE DELETION IN A TYPE OF 5^O-BETA ^O-THALASSAEMIA BEGINS IN AN INVERTED ALU I REPEATOTTOLENGHI S; GIGLIONI B.1982; NATURE (LONDON); ISSN 0028-0836; GBR; DA. 1982; VOL. 300; NO 5894; PP. 770-771; BIBL. 22 REF.Article

DISSOCIATION OF SINGLE RIBOSOMES AS A PRELIMINARY STEP FOR THEIR PARTICIPATION IN PROTEIN SYNTHESISOTTOLENGHI S; COMI P; GIGLIONI B et al.1973; EUROP. J. BIOCHEM.; GERM.; DA. 1973; VOL. 33; NO 2; PP. 227-232; BIBL. 26 REF.Serial Issue

INHIBITION OF PROTEIN SYNTHESIS BY ALIPHATIC ALDEHYDES. FAILURE OF 2,3-DIHYDROXYBUTYRALDEHYDE TO INHIBIT CHAIN INITIATION IN RETICULOCYTE LYSATESCOMI P; OTTOLENGHI S; GIANNI AM et al.1973; BIOCHIMIE; FR.; DA. 1973; VOL. 55; NO 4; PP. 507-508; BIBL. 8 REF.Serial Issue

TRANSCRIPTIONAL AND POST-TRANSCRIPTIONAL DEFECTS IN BETA ^O-THALASSAEMIA.COMI P; GIGLIONI B; BARBARANO L et al.1977; EUROP. J. BIOCHEM.; GERM.; DA. 1977; VOL. 79; NO 2; PP. 617-622; BIBL. 28 REF.Article

GLOBIN RNA SEQUENCES IN HUMAN LEUKAEMIC PERIPHERAL BLOODGIANNI AM; DELLA FAVERA R; POLLI E et al.1978; NATURE; GBR; DA. 1978; VOL. 274; NO 5671; PP. 610-612; BIBL. 13 REF.Article

BETA -LIBRE GLOBIN RNA SEQUENCES IN HEMOGLOBIN LEPORE DISEASEGIGLIONI B; COMI P; TARAMELLI R et al.1979; EUROP. J. BIOCHEM.; DEU; DA. 1979; VOL. 95; NO 3; PP. 527-531; BIBL. 17 REF.Article

GLOBIN GENE DELETION IN HPFH, DELTA ^OBETA ^O THALASSAEMIA AND HB LEPORE DISEASEOTTOLENGHI S; GIGLIONI B; COMI P et al.1978; NATURE; GBR; DA. 1978; VOL. 278; NO 5705; PP. 654-657; BIBL. 38 REF.Article

A GENE CONTROLLING FETAL HEMOGLOBIN EXPRESSION IN ADULTS IS NOT LINKED TO THE NON-ALPHA GLOBIN CLUSTERGIANNI AM; BREGNI M; CAPPELLINI MD et al.1983; EMBO JOURNAL; ISSN 0261-4189; GBR; DA. 1983; VOL. 2; NO 6; PP. 921-925; BIBL. 26 REF.Article

DIRECT DEMONSTRATION OF BETA -GLOBIN MRNA IN HOMOZYGOUS FERRARA BETA ₀-THALASSAEMIA PATIENTS.OTTOLENGHI S; COMI P; GIGLIONI B et al.1977; NATURE; G.B.; DA. 1977; VOL. 266; NO 5599; PP. 231-234; BIBL. 26 REF.Article

DELTA THALASSEMIA: A NON-DELETION DEFECTTARAMELLI R; GIGLIONI B; COMI P et al.1983; EUROPEAN JOURNAL OF BIOCHEMISTRY; ISSN 0014-2956; DEU; DA. 1983; VOL. 129; NO 3; PP. 589-592; BIBL. 28 REF.Article

G_Y AND A_Y GLOBIN CHAINS SEPARATION AND QUANTITATION BY ISOELECTRIC FOCUSINGCOMI P; GIGLIONI B; OTTOLENGHI S et al.1979; BIOCHEM. BIOPHYS. RES. COMMUNIC.; USA; DA. 1979; VOL. 87; NO 1; PP. 1-8; BIBL. 17 REF.Article

The same nuclear proteins bind the proximal CACCC box of the human β-globin promoter and a similar sequence in the enhancerGIGLIONI, B; COMI, P; RONCHI, A et al.Biochemical and biophysical research communications (Print). 1989, Vol 164, Num 1, pp 149-155, issn 0006-291X, 7 p.Article

ISOELECTRIC FOCUSING OF GLOBIN CHAINS FOR ANTENATAL DIAGNOSIS OF BETA ⁰-THALASSEMIAGIANNI AM; POLLI E; GIGLIONI B et al.1981; HEMOGLOBIN; ISSN 0363-0269; USA; DA. 1981; VOL. 5; NO 4; PP. 349-356; BIBL. 13 REF.Article

GLOBIN CHAIN SYNTHESIS IN SINGLE ERYTHROID BURSTS FROM CORD BLOOD: STUDIES ON GAMMA ->BETA AND G_GAMMA ->A_GAMMA SWITCHESCOMI P; GIGLIONI B; OTTOLENGHI S et al.1980; PROC. NATION. ACAD. SCI.; USA; DA. 1980; VOL. 77; NO 1 PART. 1; PP. 362-365; BIBL. 40 REF.Article

PREFERENCIAL INDUCTION OF FETAL VERSUS EMBRYONIC GLOBIN CHAINS IN HUMAN LEUKEMIC CELL LINESGIANNI AM; PRESTA M; POLLI E et al.1982; LEUK. RES.; ISSN 0145-2126; USA; DA. 1982; VOL. 6; NO 2; PP. 155-163; BIBL. 24 REF.Article

PRESENCE OF GENE FOR BETA GLOBIN IN HOMOZYGOUS BETA ₀THALASSAEMIA = PRESENCE DU GENE POUR LA BETA -GLOBINE DANS LA BETA ₀THALASSEMIE HOMOZYGOTETOLSTOSHEV P; MITCHELL J; LANYON G et al.1976; NATURE; G.B.; DA. 1976; VOL. 259; NO 5539; PP. 95-98; BIBL. 16 REF.Article

DELTA BETA -THALASSEMIA IS DUE TO A GENE DELETION.OTTOLENGHI S; COMI P; GIGLIONI B et al.1976; CELL; U.S.A.; DA. 1976; VOL. 9; NO 1; PP. 71-80; BIBL. 1 P.Article

A DIRECT ESTIMATE OF THE NUMBER OF HUMAN GAMMA -GLOBIN GENES.OLD J; CLEGG JB; WEATHERALL DJ et al.1976; CELL; U.S.A.; DA. 1976; VOL. 8; NO 1; PP. 13-18; BIBL. 26 REF.Article

MOLECULAR COMPARISON OF DELTA BETA -THALASSEMIA AND HEREDITARY PERSISTANCE OF FETAL HEMOGLOBIN DNAS: EVIDENCE OF A REGULATORY AREA.OTTOLENGHI S; GIGLIONI B; TARAMELLI R et al.1982; PROC. NATL. ACAD. SCI. U.S.A., BIOL. SCI.; ISSN 0273-1134; USA; DA. 1982; VOL. 79; NO 7; PP. 2347-2351; BIBL. 32 REF.Article

BIOSYNTHESIS OF GLOBIN CHAINS IN FETAL LIVER AND ADULT MARROW CULTURES: COMPARATIVE ANALYSIS OF INDIVIDUAL COLONIES DERIVED FROM EARLY, INTERMEDIATE OR LATE ERYTHROID PROGENITORSCOMI P; GIGLIONI B; POZZOLI ML et al.1981; EXP. CELL. RES.; ISSN 0014-4827; USA; DA. 1981; VOL. 133; NO 2; PP. 347-356; BIBL. 25 REF.Article

HEMOGLOBIN SYNTHESIS IN INDIVIDUAL BURSTS FROM NORMAL ADULT BLOOD: ALL BURSTS AND SUBCOLONIES SYNTHESIZE ^GGAMMA - AND ^AGAMMA -GLOBIN CHAINSPESCHLE C; MIGLIACCIO G; COVELLI A et al.1980; BLOOD; ISSN 0006-4971; USA; DA. 1980; VOL. 56; NO 2; PP. 218-226; BIBL. 33 REF.Article

BIOSYNTHESIS OF HB IN INDIVIDUAL FETAL LIVER BURSTS: GAMMA -CHAIN PRODUCTION PEAKS EARLIER THAN BETA -CHAIN IN THE ERYTHROPOIETIC PATHWAYGIANNI AM; COMI P; GIGLIONI B et al.1980; EXP. CELL RES.; ISSN 0014-4827; USA; DA. 1980; VOL. 130; NO 2; PP. 345-352; BIBL. 21 REF.Article

DNA sequences regulating human globin gene transcription in nondeletional hereditary persistence of fetal hemoglobinOTTOLENGHI, S; MANTOVANI, R; NICOLIS, S et al.Hemoglobin. 1989, Vol 13, Num 6, pp 423-541, issn 0363-0269Article

A protein factor binding to an octamer motif in the γ-globin promoter disappears upon induction of differentiation and hemoglobin synthesis in K562 cellsMANTOVANI, R; MALGARETTI, N; GIGLIONI, B et al.Nucleic acids research. 1987, Vol 15, Num 22, pp 9349-9364, issn 0305-1048Article

Increased erythroid-specific expression of a mutated HPFH γ-globin promoter requires the erythroid factor NFE-1NICOLIS, S; RONCHI, A; MALGARETTI, N et al.Nucleic acids research. 1989, Vol 17, Num 14, pp 5509-5516, issn 0305-1048, 8 p.Article