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au.\*:("OTTOLENGHI S")

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THE DELETION IN A TYPE OF 5O-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

HUMAN GLOBIN GENE EXPRESSION AND LINKAGE IN BONE MARROW AND FETAL LIVER.LANYON WG; OTTOLENGHI S; WILLIAMSON R et al.1975; PROC. NATION. ACAD. SCI. U.S.A.; U.S.A.; DA. 1975; VOL. 72; NO 1; PP. 258-262; BIBL. 30 REF.Article

PLEIOTROPIC, EXTRAGENIC SUPPRESSION OF DNA MUTATIONS IN BACILLUS SUBTILIS.SICCARDI AG; OTTOLENGHI S; FORTUNATO A et al.1976; J. BACTERIOL.; U.S.A.; DA. 1976; VOL. 128; NO 1; PP. 174-181; BIBL. 26 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

The structure of regional councils in Israel : some legal and organizational problemsOTTOLENGHI, S; WILKANSKY, R.Planning and Administration. 1986, Vol 13, Num 2, pp 21-25Article

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

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

GY AND AY 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

GENE DELETION AS THE CAUSE OF ALPHA THALASSAEMIA: THE SEVERE FORM OF ALPHA THALASSAEMIA IS CAUSED BY A HAEMOGLOBIN GENE DELETION = DELETION DE GENE, CAUSE DE L'ALPHA -THALASSEMIEOTTOLENGHI S; LANYON WG; PAUL J et al.1974; NATURE; G.B.; DA. 1974; VOL. 251; NO 5474; PP. 389-392; BIBL. 33REF.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

POLYMORPHISMS OF HUMAN GAMMA -GLOBIN GENES IN MEDITERRANEAN POPULATIONSLITTLE PFR; WILLIAMSON R; ANNISON G et al.1979; NATURE; GBR; DA. 1979; VOL. 282; NO 5736; PP. 316-318; BIBL. 25 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

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 GGAMMA ->AGAMMA 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

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

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 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

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

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