Martini G - Search Results

1

Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.

Vulliamy TJ, D'Urso M, Battistuzzi G, Estrada M, Foulkes NS, Martini G, Calabro V, Poggi V, Giordano R, Town M, et al. Vulliamy TJ, et al. Among authors: martini g. Proc Natl Acad Sci U S A. 1988 Jul;85(14):5171-5. doi: 10.1073/pnas.85.14.5171. Proc Natl Acad Sci U S A. 1988. PMID: 3393536 Free PMC article.

2

Specific methylation pattern at the 3' end of the human housekeeping gene for glucose 6-phosphate dehydrogenase.

Toniolo D, D'Urso M, Martini G, Persico M, Tufano V, Battistuzzi G, Luzzatto L. Toniolo D, et al. Among authors: martini g. EMBO J. 1984 Sep;3(9):1987-95. doi: 10.1002/j.1460-2075.1984.tb02080.x. EMBO J. 1984. PMID: 6092050 Free PMC article.

3

Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysis.

Calabrò V, Mason PJ, Filosa S, Civitelli D, Cittadella R, Tagarelli A, Martini G, Brancati C, Luzzatto L. Calabrò V, et al. Among authors: martini g. Am J Hum Genet. 1993 Mar;52(3):527-36. Am J Hum Genet. 1993. PMID: 8447319 Free PMC article.

4

Isolation of human glucose-6-phosphate dehydrogenase (G6PD) cDNA clones: primary structure of the protein and unusual 5' non-coding region.

Persico MG, Viglietto G, Martini G, Toniolo D, Paonessa G, Moscatelli C, Dono R, Vulliamy T, Luzzatto L, D'Urso M. Persico MG, et al. Among authors: martini g. Nucleic Acids Res. 1986 Mar 25;14(6):2511-22. doi: 10.1093/nar/14.6.2511. Nucleic Acids Res. 1986. PMID: 3515319 Free PMC article.

5

Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase.

Martini G, Toniolo D, Vulliamy T, Luzzatto L, Dono R, Viglietto G, Paonessa G, D'Urso M, Persico MG. Martini G, et al. EMBO J. 1986 Aug;5(8):1849-55. doi: 10.1002/j.1460-2075.1986.tb04436.x. EMBO J. 1986. PMID: 2428611 Free PMC article.

6

Molecular basis of chronic non-spherocytic haemolytic anaemia: a new G6PD variant (393 Arg----His) with abnormal KmG6P and marked in vivo instability.

Filosa S, Calabrò V, Vallone D, Poggi V, Mason P, Pagnini D, Alfinito F, Rotoli B, Martini G, Luzzatto L, et al. Filosa S, et al. Among authors: martini g. Br J Haematol. 1992 Jan;80(1):111-6. doi: 10.1111/j.1365-2141.1992.tb06409.x. Br J Haematol. 1992. PMID: 1536798

7

G6PD haplotypes spanning Xq28 from F8C to red/green color vision.

Filosa S, Calabrò V, Lania G, Vulliamy TJ, Brancati C, Tagarelli A, Luzzatto L, Martini G. Filosa S, et al. Among authors: martini g. Genomics. 1993 Jul;17(1):6-14. doi: 10.1006/geno.1993.1276. Genomics. 1993. PMID: 8104869

8

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 site.

Szabo P, Purrello M, Rocchi M, Archidiacono N, Alhadeff B, Filippi G, Toniolo D, Martini G, Luzzatto L, Siniscalco M. Szabo P, et al. Among authors: martini g. Proc Natl Acad Sci U S A. 1984 Dec;81(24):7855-9. doi: 10.1073/pnas.81.24.7855. Proc Natl Acad Sci U S A. 1984. PMID: 6595664 Free PMC article.

9

High-level regulated expression of the human G6PD gene in transgenic mice.

Corcoran CM, Fraser P, Martini G, Luzzatto L, Mason PJ. Corcoran CM, et al. Among authors: martini g. Gene. 1996 Sep 16;173(2):241-6. doi: 10.1016/0378-1119(96)00094-7. Gene. 1996. PMID: 8964507 Free article.

10

Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency.

Filosa S, Giacometti N, Wangwei C, De Mattia D, Pagnini D, Alfinito F, Schettini F, Luzzatto L, Martini G. Filosa S, et al. Among authors: martini g. Am J Hum Genet. 1996 Oct;59(4):887-95. Am J Hum Genet. 1996. PMID: 8808605 Free PMC article.

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