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20 results for author:"Bianchi V." in Literature citations

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Mammalian ribonucleotide reductase subunit p53R2 is required for mitochondrial DNA replication and DNA repair in quiescent cells.

Pontarin G., Ferraro P., Bee L., Reichard P., Bianchi V.

Proc. Natl. Acad. Sci. U.S.A. 109:13302-13307(2012) · Mapped (3)

Forebrain deletion of alphaGDI in adult mice worsens the pre-synaptic deficit at cortico-lateral amygdala synaptic connections.

Bianchi V., Gambino F., Muzio L., Toniolo D., Humeau Y., D'Adamo P.

PLoS ONE 7:e29763-e29763(2012) · Mapped (2)

Growth defects and impaired cognitive-behavioral abilities in mice with knockout for Eif4h, a gene located in the mouse homolog of the Williams-Beuren syndrome critical region.

Capossela S., Muzio L., Bertolo A., Bianchi V., Dati G., Chaabane L., Godi C., Politi L.S., Biffo S., D'Adamo P. et al.

Am. J. Pathol. 180:1121-1135(2012) · Mapped (4)

Deoxyribonucleotide metabolism in cycling and resting human fibroblasts with a missense mutation in p53R2, a subunit of ribonucleotide reductase.

Pontarin G., Ferraro P., Rampazzo C., Kollberg G., Holme E., Reichard P., Bianchi V.

J. Biol. Chem. 286:11132-11140(2011) · Mapped (3)

Nuclear damage in peripheral lymphocytes of obese and overweight Italian children as evaluated by the gamma-H2AX focus assay and micronucleus test.

Scarpato R., Verola C., Fabiani B., Bianchi V., Saggese G., Federico G.

FASEB J. 25:685-693(2011) · Mapped (1)

Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly.

Giannandrea M., Bianchi V., Mignogna M.L., Sirri A., Carrabino S., D'Elia E., Vecellio M., Russo S., Cogliati F., Larizza L. et al.

Am. J. Hum. Genet. 86:185-195(2010) · UniProtKB (2) · Mapped (4)

Use of carbohydrate-deficient transferrin (CDT) and a combination of GGT and CDT (GGT-CDT) to assess heavy alcohol consumption in traffic medicine.

Bianchi V., Ivaldi A., Raspagni A., Arfini C., Vidali M.

Alcohol Alcohol. 45:247-251(2010) · Mapped (9)

Cognitive impairment in Gdi1-deficient mice is associated with altered synaptic vesicle pools and short-term synaptic plasticity, and can be corrected by appropriate learning training.

Bianchi V., Farisello P., Baldelli P., Meskenaite V., Milanese M., Vecellio M., Muhlemann S., Lipp H.P., Bonanno G., Benfenati F. et al.

Hum. Mol. Genet. 18:105-117(2009) · Mapped (3)

Crystal structures of human and murine deoxyribonucleotidases: insights into recognition of substrates and nucleotide analogues.

Wallden K., Rinaldo-Matthis A., Ruzzenente B., Rampazzo C., Bianchi V., Nordlund P.

Biochemistry 46:13809-13818(2007) · UniProtKB (2) · Mapped (1)

Crystal structure of human cytosolic 5'-nucleotidase II: insights into allosteric regulation and substrate recognition.

Wallden K., Stenmark P., Nyman T., Flodin S., Graeslund S., Loppnau P., Bianchi V., Nordlund P.

J. Biol. Chem. 282:17828-17836(2007) · UniProtKB (2) · Mapped (3)

Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian population.

Bianchi V., Maconi G., Ardizzone S., Colombo E., Ferrara E., Russo A., Tenchini M.L., Porro G.B.

Eur J Gastroenterol Hepatol 19:217-223(2007) · Mapped (8)

Multidrug resistance 1 gene polymorphism and susceptibility to inflammatory bowel disease.

Ardizzone S., Maconi G., Bianchi V., Russo A., Colombo E., Cassinotti A., Penati C., Tenchini M.L., Bianchi Porro G.

Inflamm. Bowel Dis. 13:516-523(2007) · Mapped (9)

Structural basis for substrate specificity of the human mitochondrial deoxyribonucleotidase.

Wallden K., Ruzzenente B., Rinaldo-Matthis A., Bianchi V., Nordlund P.

Structure 13:1081-1088(2005) · Mapped (2)

Crystal structures of the mitochondrial deoxyribonucleotidase in complex with two specific inhibitors.

Rinaldo-Matthis A., Rampazzo C., Balzarini J., Reichard P., Bianchi V., Nordlund P.

Mol. Pharmacol. 65:860-867(2004) · Mapped (1)

Crystal structure of a human mitochondrial deoxyribonucleotidase.

Rinaldo-Matthis A., Rampazzo C., Reichard P., Bianchi V., Nordlund P.

Nat. Struct. Biol. 9:779-787(2002) · UniProtKB (1) · Mapped (1)

Mouse cytosolic and mitochondrial deoxyribonucleotidases: cDNA cloning of the mitochondrial enzyme, gene structures, chromosomal mapping and comparison with the human orthologs.

Rampazzo C., Kost-Alimova M., Ruzzenente B., Dumanski J.P., Bianchi V.

Gene 294:109-117(2002) · UniProtKB (3) · Mapped (1)

Human mitochondrial 5'-deoxyribonucleotidase. Overproduction in cultured cells and functional aspects.

Gallinaro L., Crovatto K., Rampazzo C., Pontarin G., Ferraro P., Milanesi E., Reichard P., Bianchi V.

J. Biol. Chem. 277:35080-35087(2002) · Mapped (2)

A deoxyribonucleotidase in mitochondria: involvement in regulation of dNTP pools and possible link to genetic disease.

Rampazzo C., Gallinaro L., Milanesi E., Frigimelica E., Reichard P., Bianchi V.

Proc. Natl. Acad. Sci. U.S.A. 97:8239-8244(2000) · UniProtKB (1)

Mammalian 5'(3')-deoxyribonucleotidase, cDNA cloning, and overexpression of the enzyme in Escherichia coli and mammalian cells.

Rampazzo C., Johansson M., Gallinaro L., Ferraro P., Hellman U., Karlsson A., Reichard P., Bianchi V.

J. Biol. Chem. 275:5409-5415(2000) · UniProtKB (2) · Mapped (1)

Escherichia coli ferredoxin NADP+ reductase: activation of E. coli anaerobic ribonucleotide reduction, cloning of the gene (fpr), and overexpression of the protein.

Bianchi V., Reichard P., Eliasson R., Pontis E., Krook M., Joernvall H., Haggaard-Ljungquist E.

J. Bacteriol. 175:1590-1595(1993) · UniProtKB (1)

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