G. Martini

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Glucose-6-phosphate dehydrogenase plays a crucial role in protection from redox-stress-induced apoptosis

P. Verde, L. Cigliano, I. Iaccarino, 2004, Cell Death and Differentiation.

Enhanced expression of glucose-6-phosphate dehydrogenase in human cells sustaining oxidative stress.

G. Martini, S. Salzano, M. Ursini, 1997, The Biochemical journal.

Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG islands within 100 kb of DNA.

B. Migeon, D. Toniolo, G. Martini, 1988, The EMBO journal.

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

V. Poggi, G. Battistuzzi, L. Luzzatto, 1992, British journal of haematology.

An Ig Transmembrane Domain Motif Improves the Function of TCRs Transduced in Human T Cells: Implications for Immunotherapy

P. Circosta, G. Martini, R. Sartorius, 2019, Journal of immunotherapy.

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

P. Fraser, L. Luzzatto, G. Martini, 1996, Gene.

Mapping of human thyroglobulin gene on the long arm of chromosome 8 by in situ hybridization

E. Calzolari, R. Lauro, A. Monticelli, 2004, Human Genetics.

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

M. D'urso, G. Viglietto, T. Vulliamy, 1986, The EMBO journal.

High levels of transcription driven by a 400 bp segment of the human G6PD promoter.

G. Martini, M. Ursini, L. Scalera, 1990, Biochemical and biophysical research communications.

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

M. D'urso, V. Poggi, T. Vulliamy, 1988, Proceedings of the National Academy of Sciences of the United States of America.

A novel single-base mutation in the glucose 6-phosphate dehydrogenase gene is associated with chronic non-spherocytic haemolytic anaemia

G. Martini, A. Cao, R. Galanello, 1994, Human Genetics.

2-deoxy-d-ribose induces apoptosis by inhibiting the synthesis and increasing the efflux of glutathione.

C. Franceschi, L. Cigliano, A. Fico, 2008, Free radical biology & medicine.

Fungal extrachromosomal DNA and its maintenance and expression in E. coli K-12

J. Guardiola, G. Martini, G. Grimaldi, 1978 .

The CpG island in the 5' region of the G6PD gene of man and mouse.

D. Toniolo, G. Martini, T. Lettieri, 1991, Gene.

Failure to increase glucose consumption through the pentose-phosphate pathway results in the death of glucose-6-phosphate dehydrogenase gene-deleted mouse embryonic stem cells subjected to oxidative stress.

José M Bautista, Stefania Filosa, P. Verde, 2003, The Biochemical journal.

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

M. D'urso, G. Viglietto, T. Vulliamy, 1986, Nucleic acids research.

G6PD is indispensable for erythropoiesis after the embryonic-adult hemoglobin switch.

L. Luzzatto, I. Iaccarino, A. Fico, 2004, Blood.

Localization of glucose-6-phosphate dehydrogenase in mouse and man by in situ hybridization: evidence for a single locus and transposition of homologous X-linked genes.

B. Migeon, D. Toniolo, G. Martini, 1985, Cytogenetics and cell genetics.

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

M. D'urso, G. Battistuzzi, L. Luzzatto, 1984, The EMBO journal.

Isolation and Analysis of Genomic Sequences from Mycorrhizal Fungi

G. Martini, S. Filosa, A. Franzè, 1995 .

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

L. Luzzatto, G. Martini, S. Filosa, 1996, American journal of human genetics.

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

T. Vulliamy, L. Luzzatto, G. Martini, 1993, Genomics.

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

L. Luzzatto, G. Martini, S. Filosa, 1993, American journal of human genetics.

Genetic variation in the host and adaptive phenomena in Plasmodium falciparum infection.

L. Luzzatto, G. Martini, O. Sodeinde, 1983, Ciba Foundation symposium.

Molecular characterization of G6PD deficiency in Southern Italy: heterogeneity, correlation genotype–phenotype and description of a new variant (G6PD Neapolis)

L. Vitagliano, A. Zagari, A. Cimmino, 1997, British journal of haematology.

A new lease of life for an old enzyme

G. Martini, M. Ursini, M V Ursini, 1996, BioEssays : news and reviews in molecular, cellular and developmental biology.

ANALYSIS OF THE PRIMARY STRUCTURE OF HUMAN G6PD DEDUCED FROM THE cDNA SEQUENCE

M. D'urso, G. Viglietto, T. Vulliamy, 1986 .

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.

N. Archidiacono, M. Rocchi, L. Luzzatto, 1984, Proceedings of the National Academy of Sciences of the United States of America.

DNA haplotypes in the G6PD gene cluster studied in the Chinese Li population and their relationship to G6PDCanton.

G. Martini, S. Filosa, W. Cai, 1994, Human heredity.

Molecular anatomy of the human glucose 6‐phosphate dehydrogenase core promoter

G. Martini, M. Ferrante, M. Ursini, 1998, FEBS letters.

Functional expression of human glucose-6-phosphate dehydrogenase in Escherichia coli.

A. Ciccodicola, G. Martini, M. Persico, 1989, Gene.

Enhanced activity of human G6PD promoter transfected in HeLa cells producing high levels of HIV-1 Tat.

M. Braddock, G. Martini, M. Ursini, 1993, Virology.