Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("MARENI C")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 30

  • Page / 2
Export

Selection :

  • and

FRAGILE X SYNDROME: SEARCH FOR PHENOTYPIC MANIFESTATIONS AT LOCI FOR HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE AND GLUCOSE-6-PHOSPHATE DEHYDROGENASEMARENI C; MIGEON BR.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 5; PP. 752-761; BIBL. 24 REF.Article

EFFECT OF HAEMOLYSIS ON THE HEXOSE-MONOPHOSPHATE PATHWAY IN NORMAL AND IN GLUCOSE-6-PHOSPHATE DEHYDROGENASE-DEFICIENT ERYTHROCYTES.GALIANO S; MARENI C; GAETANI GFD et al.1978; BIOCHIM. BIOPHYS. ACTA; PAYS BAS; DA. 1978; VOL. 501; NO 1; PP. 1-9; BIBL. 18 REF.Article

RED CELL NADP+ AND NADPH IN GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY = NADP+ ET NADPH DES HEMATIES DANS LE DEFICIT EN GLUCOSE 6 PHOSPHATE DESHYDROGENASEKIRKMAN HN; GAETANI GD; CLEMONS EH et al.1975; J. CLIN. INVEST.; U.S.A.; DA. 1975; VOL. 55; NO 4; PP. 875-878; BIBL. 12REF.Article

NEW GENETIC VARIANTS OF GLUCOSE 6-PHOSPHATE DEHYDROGENASE (G6PD) IN ITALYSANSONE G; PERRONI L; TESTA U et al.1981; ANN. HUM. GENET.; ISSN 0003-4800; GBR; DA. 1981; VOL. 45; PART. 2; PP. 97-104; BIBL. 17 REF.Article

A NEW GLUCOSE 6-PHOSPHATE DEHYDROGENASE VARIANT (G-6-PD VERONA) IN A PATIENT WITH MYELODYSPLASTIC SYNDROMEPERONA G; GUIDI GC; TUMMARELLO D et al.1983; SCANDINAVIAN JOURNAL OF HAEMATOLOGY; ISSN 0036-553X; DNK; DA. 1983; VOL. 30; NO 5; PP. 407-414; BIBL. 2 P.Article

FAVISM: ERYTHROCYTE METABOLISM DURING HAEMOLYSIS AND RETICULOCYTOSISGAETANI GF; MARENI C; SALVIDIO E et al.1979; BRIT. J. HAEMATOL.; GBR; DA. 1979; VOL. 43; NO 1; PP. 39-48; BIBL. 26 REF.Article

REGULATION OF GLUCOSE 6-PHOSPHATE DEHYDROGENASE EXPRESSION IN CHO-HUMAN FIBROBLAST SOMATIC CELL HYBRIDSD'URSO M; MARENI C; TONIOLO D et al.1983; SOMATIC CELL GENETICS; ISSN 0098-0366; USA; DA. 1983; VOL. 9; NO 4; PP. 429-443; BIBL. 27 REF.Article

RADIOIMMUNOASSAY AND CHEMICAL PROPERTIES OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE AND OF A SPECIFIC NADP (H)-BINDING PROTEIN (FX) FROM HUMAN ERYTHROCYTES.DE FLORA A; MORELLI A; FRASCIO M et al.1977; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1977; VOL. 500; NO 1; PP. 109-123; BIBL. 37 REF.Article

Derepression with decreased expression of the G6PD locus on the inactive X chromosome in normal human cellsMIGEON, B. R; WOLF, S. F; MARENI, C et al.Cell (Cambridge). 1982, Vol 29, Num 2, pp 595-600, issn 0092-8674Article

Favism: looking for an autosomal gene associated with glucose-6-phosphate dehydrogenase deficiencyMARENI, C; REPETTO, L; FORTELEONI, G et al.Journal of medical genetics. 1984, Vol 21, Num 4, pp 278-280, issn 0022-2593Article

Cytogenetic follow-up after bone marrow transplantation for Philadelpnia-positive chronic myeloid leukemiaSESSAREGO, M; FRASSONI, F; DEFFERRARI, R et al.Cancer genetics and cytogenetics. 1989, Vol 42, Num 2, pp 253-261, issn 0165-4608Article

Translocation t(9;9)(p13;q34) in Philadelphia-negative chronic myeloid leukemia with breakpoint cluster region rearrangementSESSAREGO, M; MARENI, C; VIMERCATI, R et al.Cancer genetics and cytogenetics. 1989, Vol 43, Num 1, pp 51-56, issn 0165-4608Article

Exclusion of the APC gene as the cause of a variant form of familial adenomatous polyposis (FAP)STELLA, A; RESTA, N; GENTILE, M et al.American journal of human genetics. 1993, Vol 53, Num 5, pp 1031-1037, issn 0002-9297Article

Early and long term follow-up with minisatellite probes in bone marrow transplanted patientsMARENI, C; ORIGONE, P; SESSAREGO, M et al.Leukemia. 1990, Vol 4, Num 10, pp 704-707, issn 0887-6924, 4 p.Article

Recombinant human erythropoietin for long-term treatment of anemia in paroxysmal nocturnal hemoglobinuriaBALLEARI, E; GATTI, A. M; MARENI, C et al.Haematologica (Roma). 1996, Vol 81, Num 2, pp 143-147, issn 0390-6078Article

Acute myelogenous leukemia with translocation t(8;21): a cytogenetic study of seven casesSESSAREGO, M; MARENI, C; PANARELLO, C et al.Cancer genetics and cytogenetics. 1986, Vol 20, Num 3-4, pp 363-368, issn 0165-4608Article

Involvement of chromosomal region 9q34 in a case of variant Ph1 translocation t(22;22)MARENI, C; SESSAREGO, M; COVIELLO, D. A et al.Leukemia research. 1986, Vol 10, Num 9, pp 1131-1137, issn 0145-2126Article

Molecular analysis of Philadelphia-negative myeloproliferative syndromes with i(17q)MARENI, C; SESSAREGO, M; ORIGONE, P et al.Cancer genetics and cytogenetics. 1989, Vol 43, Num 2, pp 195-201, issn 0165-4608Article

Reexpression of normal stem cells in erythroleukemia during remission = Réexpression des cellules souches normales dans l'érythroleucémie en phase de rémissionFERRARIS, A. M; CANEPA, L; MARENI, C et al.Blood. 1983, Vol 62, Num 1, pp 177-179, issn 0006-4971Article

Amplification of c-myc and put-1 homologous sequences in acute nonlymphatic leukemiaASKER, C; MARENI, C; COVIELLO, D et al.Leukemia research. 1988, Vol 12, Num 6, pp 523-527, issn 0145-2126Article

Subcutaneous recombinant human erythropoietin for the treatment of anemia in myelodysplastic syndromesGHIO, R; BALLEARI, E; BALLESTRERO, A et al.Acta haematologica. 1993, Vol 90, Num 2, pp 58-64, issn 0001-5792Article

Karyotype evolution of Ph positive chronic myelogenous leukemia patients relapsed in advanced phases of the disease after allogeneic bone marrow transplantationSESSAREGO, M; FRASSONI, F; DEFFERRARI, R et al.Cancer genetics and cytogenetics. 1991, Vol 57, Num 1, pp 69-78, issn 0165-4608Article

A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instabilityMARRONI, F; PASTRELLO, C; BAILEY-WILSON, J. E et al.Clinical genetics. 2006, Vol 69, Num 3, pp 254-262, issn 0009-9163, 9 p.Article

Clinical findings in a family with familial adenomatous polyposis and a missense mutation of the adenomatous polyposis coli geneMARCHESE, C. A; BERTOLINO, F; GUANTI, G et al.Scandinavian journal of gastroenterology. 1996, Vol 31, Num 9, pp 917-920, issn 0036-5521Article

STKII mutations in Peutz-Jeghers syndrome and sporadic colon cancerRESTA, N; SIMONE, C; CARLOMAGNO, N et al.Cancer research (Baltimore). 1998, Vol 58, Num 21, pp 4799-4801, issn 0008-5472Article

  • Page / 2