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CDNA SEQUENCES OF HUMAN GLUCOSE 6-PHOSPHATE DEHYDROGENASE CLONED IN PBR 322 = SEQUENCES D'ADNC DE LA GLUCOSE PHOSPHATE-6 DESHYDROGENASE HUMAINE CLONEES DANS PBR 322PERSICO MG; TONIOLO D; NOBILE C et al.1981; NATURE (LOND.); ISSN 0028-0836; GBR; DA. 1981; VOL. 294; NO 5843; PP. 778-780; BIBL. 33 REF.Article

CpG islands of the X chromosome are gene associatedALCALAY, M; TONIOLO, D.Nucleic acids research. 1988, Vol 16, Num 20, pp 9527-9543, issn 0305-1048Article

FAST-NEUTRON TRANSMISSION THROUGH A POLARIZED HOLMIUM TARGETFASOLI U; GALEAZZI G; TONIOLO D et al.1973; LETTERE NUOVO CIMENTO; ITAL.; DA. 1973; VOL. 6; NO 13; PP. 485-490; BIBL. 8 REF.Serial Issue

NEUTRON-CARBON INTERACTION: TOTAL AND ELASTIC SCATTERING DIFFERENTIAL CROSS SECTIONS AND PHASE SHIFT ANALYSIS, 2.1 TO 4.7 MEVFASOLI U; METELLINI A; TONIOLO D et al.1973; NUCL. PHYS., A; NETHERL.; DA. 1973; VOL. 205; NO 2; PP. 305-320; BIBL. 26 REF.Serial Issue

SOLITON FISSION AND TUNNELLING IN ELECTRIC LINESBON P; MINELLI TA; PASCOLINI A et al.1982; LETT. NUOVO CIMENTO SOC. ITAL. FIS.; ISSN 0375-930X; ITA; DA. 1982; VOL. 35; NO 9; PP. 279-284; BIBL. 7 REF.Article

Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestationBODEGA, B; BIONE, S; DALPRA, L et al.Human reproduction (Oxford. Print). 2006, Vol 21, Num 4, pp 952-957, issn 0268-1161, 6 p.Article

Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1BBIONE, S; RIZZOLIO, F; CROSIGNANI, P. G et al.Human reproduction (Oxford. Print). 2004, Vol 19, Num 12, pp 2759-2766, issn 0268-1161, 8 p.Article

A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure : Evidence for conserved function in oogenesis and implications for human sterilityBIONE, S; SALA, C; BALLABIO, A et al.American journal of human genetics. 1998, Vol 62, Num 3, pp 533-541, issn 0002-9297Article

Ultrastructural abnormality of sarcolemmal nuclei in Emery-Dreifuss muscular dystrophy (EDMD)FIDZIANSKA, A; TONIOLO, D; HAUSMANOWA-PETRUSEWICZ, I et al.Journal of the neurological sciences. 1998, Vol 159, Num 1, pp 88-93, issn 0022-510XArticle

X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sampleMORA, M; CARTEGNI, L; DONATI, M. A et al.Annals of neurology. 1997, Vol 42, Num 2, pp 249-253, issn 0364-5134Article

Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the diseaseBIONE, S; SMALL, K; TONIOLO, D et al.Human molecular genetics (Print). 1995, Vol 4, Num 10, pp 1859-1863, issn 0964-6906Article

Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)ROUSSEAU, F; VINCENT, A; TONIOLO, D et al.American journal of human genetics. 1991, Vol 48, Num 1, pp 108-116, issn 0002-9297, 9 p.Article

Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathyBENEDETTI, S; BERTINI, E; QUATTRINI, A et al.Journal of neurology, neurosurgery and psychiatry. 2005, Vol 76, Num 7, pp 1019-1021, issn 0022-3050, 3 p.Article

Transcriptional organization of a 450-kb region of the human X chromosome in Xq28BIONE, S; TAMANINI, F; MAESTRINI, E et al.Proceedings of the National Academy of Sciences of the United States of America. 1993, Vol 90, Num 23, pp 10977-10981, issn 0027-8424Article

Identification of novel RFLPs in the vicinity of CpG islands in Xq28 : application to the analysis of the pattern of X chromosome inactivationMAESTRINI, E; RIVELLA, S; TRIBIOLI, C et al.American journal of human genetics. 1992, Vol 50, Num 1, pp 156-163, issn 0002-9297Article

Methylation and sequence analysis around eagi sites : identification of 28 new CpG islands in XQ24-XQ28TRIBIOLI, C; TAMANINI, F; VEZZONI, P et al.Nucleic acids research. 1992, Vol 20, Num 4, pp 727-733, issn 0305-1048Article

Stability of DNA methylation of X-chromosome genes during agingPAGANI, F; TONIOLO, D; VERGANI, C et al.Somatic cell and molecular genetics. 1990, Vol 16, Num 1, pp 79-84, issn 0740-7750Article

Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG islands within 100 kb of DNATONIOLO, D; MARTINI, G; MIGEON, B. R et al.EMBO journal (Print). 1988, Vol 7, Num 2, pp 401-406, issn 0261-4189Article

Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this siteSZABO, P; PURRELLO, M; ROCCHI, M et al.Proceedings of the National Academy of Sciences of the United States of America. Biological sciences. 1984, Vol 81, Num 24, pp 7855-7859, issn 0273-1134Article

Complete concordance between glucose-6-phosphate dehydrogenase activity and hypomethylation of 3' CpG clusters: implications for X chromosome dosage compensationWOLF, S. F; DINTZIS, S; TONIOLO, D et al.Nucleic acids research. 1984, Vol 12, Num 24, pp 9333-9348, issn 0305-1048Article

Selection and mapping of replication origins from a 500-kb region of the human X chromosome and their relationship to gene expressionRIVELLA, S; PALERMO, B; PELIZON, C et al.Genomics (San Diego, Calif.). 1999, Vol 62, Num 1, pp 11-20, issn 0888-7543Article

Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitorBIENVENU, T; PORTES, V. D; MORAINE, C et al.Human molecular genetics (Print). 1998, Vol 7, Num 8, pp 1311-1315, issn 0964-6906Article

X chromosome inactivation in carriers of Barth syndromeØRSTAVIK, K. H; ØRSTAVIK, R. E; NAUMOVA, A. K et al.American journal of human genetics. 1998, Vol 63, Num 5, pp 1457-1463, issn 0002-9297Article

X-linked severe mental retardation and a progressive neurological disorder in a Belgian family : clinical and genetic studiesCLAES, S; DEVRIENDT, K; D'ADAMO, P et al.Clinical genetics. 1997, Vol 52, Num 3, pp 155-161, issn 0009-9163Article

FISH characterization of the Xq21 breakpoint in a translocation carrier with premature ovarian failureRIVA, P; MAGNANI, I; FUHRMANN CONTI, A. M et al.Clinical genetics. 1996, Vol 50, Num 4, pp 267-269, issn 0009-9163Article

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