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11 results for author:"Carrano A.V."Drop in Literature Citations

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The DNA sequence and biology of human chromosome 19.

Grimwood J., Gordon L.A., Olsen A.S., Terry A., Schmutz J., Lamerdin J.E., Hellsten U., Goodstein D., Couronne O., Tran-Gyamfi M. et al.

Nature 428:529-535(2004) · UniProtKB (1,180)

Sequence analysis of the ERCC2 gene regions in human, mouse, and hamster reveals three linked genes.

Lamerdin J.E., Stilwagen S.A., Ramirez M.H., Stubbs L., Carrano A.V.

Genomics 34:399-409(1996) · UniProtKB (2) · Mapped (7)

Isolation and characterization of mouse Xrcc-1, a DNA repair gene affecting ligation.

Brookman K.W., Tebbs R.S., Allen S.A., Tucker J.D., Swiger R.R., Lamerdin J.E., Carrano A.V., Thompson L.H.

Genomics 22:180-188(1994) · UniProtKB (1) · Mapped (4)

Cloning and molecular characterization of the Chinese hamster ERCC2 nucleotide excision repair gene.

Kirchner J.M., Salazar E.P., Lamerdin J.E., Montgomery M.A., Carrano A.V., Weber C.A.

Genomics 23:592-599(1994) · UniProtKB (1) · Mapped (1)

Genomic sequence comparison of the human and mouse XRCC1 DNA repair gene regions.

Lamerdin J.E., Montgomery M.A., Stilwagen S.A., Scheidecker L.K., Tebbs R.S., Brookman K.W., Thompson L.H., Carrano A.V.

Genomics 25:547-554(1995) · Mapped (5)

No title

Kirchner J.M., Salazar E.P., Lamerdin J.E., Montgomery M.A., Carrano A.V., Weber C.A.

Genomics 27:387-387(1995)

Correction of a nucleotide-excision-repair mutation by human chromosome 19 in hamster-human hybrid cells.

Thompson L.H., Mooney C.L., Burkhart-Schultz K., Carrano A.V., Siciliano M.J.

Somat. Cell Mol. Genet. 11:87-92(1985) · Mapped (2)

Assignment of a human DNA-repair gene associated with sister-chromatid exchange to chromosome 19.

Siciliano M.J., Carrano A.V., Thompson L.H.

Mutat. Res. 174:303-308(1986) · Mapped (5)

Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19.

Mohrenweiser H.W., Carrano A.V., Fertitta A., Perry B., Thompson L.H., Tucker J.D., Weber C.A.

Cytogenet. Cell Genet. 52:11-14(1989) · Mapped (11)

Molecular cloning of the human XRCC1 gene, which corrects defective DNA strand break repair and sister chromatid exchange.

Thompson L.H., Brookman K.W., Jones N.J., Allen S.A., Carrano A.V.

Mol. Cell. Biol. 10:6160-6171(1990) · UniProtKB (1)

Characterization of the myotonic dystrophy region predicts multiple protein isoform-encoding mRNAs.

Jansen G., Mahadevan M.S., Amemiya C., Wormskamp N., Segers B., Hendriks W., O'Hoy K., Baird S., Sabourin L., Lennon G. et al.

Nat. Genet. 1:261-266(1992) · UniProtKB (3) · Mapped (4)

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