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23 results for author:"Lamerdin J.E."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)

Complete genome sequence of the metabolically versatile photosynthetic bacterium Rhodopseudomonas palustris.

Larimer F.W., Chain P., Hauser L., Lamerdin J.E., Malfatti S., Do L., Land M.L., Pelletier D.A., Beatty J.T., Lang A.S. et al.

Nat. Biotechnol. 22:55-61(2004) · UniProtKB (4,811)

Genome divergence in two Prochlorococcus ecotypes reflects oceanic niche differentiation.

Rocap G., Larimer F.W., Lamerdin J.E., Malfatti S., Chain P., Ahlgren N.A., Arellano A., Coleman M., Hauser L., Hess W.R. et al.

Nature 424:1042-1047(2003) · UniProtKB (4,772)

The genome of a motile marine Synechococcus.

Palenik B., Brahamsha B., Larimer F.W., Land M.L., Hauser L., Chain P., Lamerdin J.E., Regala W., Allen E.E., McCarren J. et al.

Nature 424:1037-1042(2003) · UniProtKB (2,512)

Fanconi anemia FANCG protein in mitigating radiation- and enzyme-induced DNA double-strand breaks by homologous recombination in vertebrate cells.

Yamamoto K., Ishiai M., Matsushita N., Arakawa H., Lamerdin J.E., Buerstedde J.M., Tanimoto M., Harada M., Thompson L.H., Takata M.

Mol. Cell. Biol. 23:5421-5430(2003) · UniProtKB (1) · Mapped (7)

Complete genome sequence of the ammonia-oxidizing bacterium and obligate chemolithoautotroph Nitrosomonas europaea.

Chain P., Lamerdin J.E., Larimer F.W., Regala W., Lao V., Land M.L., Hauser L., Hooper A.B., Klotz M.G., Norton J. et al.

J. Bacteriol. 185:2759-2773(2003) · UniProtKB (2,375)

Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints.

Puttagunta R., Gordon L.A., Meyer G.E., Kapfhamer D., Lamerdin J.E., Kantheti P., Portman K.M., Chung W.K., Jenne D.E., Olsen A.S. et al.

Genome Res. 10:1369-1380(2000) · Mapped (108)

Characterization of the mouse xpf DNA repair gene and differential expression during spermatogenesis.

Shannon M., Lamerdin J.E., Richardson L., McCutchen-Maloney S.L., Hwang M.H., Handel M.A., Stubbs L., Thelen M.P.

Genomics 62:427-435(1999) · UniProtKB (1) · Mapped (4)

Complex beta-satellite repeat structures and the expansion of the zinc finger gene cluster in 19p12.

Eichler E.E., Hoffman S.M., Adamson A.A., Gordon L.A., McCready P., Lamerdin J.E., Mohrenweiser H.W.

Genome Res. 8:791-808(1998) · UniProtKB (1)

Hex1: a new human Rad2 nuclease family member with homology to yeast exonuclease 1.

Wilson D.M. III, Carney J.P., Coleman M.A., Adamson A.W., Christensen M., Lamerdin J.E.

Nucleic Acids Res. 26:3762-3768(1998) · UniProtKB (1) · Mapped (3)

XRCC2 and XRCC3, new human Rad51-family members, promote chromosome stability and protect against DNA cross-links and other damages.

Liu N., Lamerdin J.E., Tebbs R.S., Schild D., Tucker J.D., Shen M.R., Brookman K.W., Siciliano M.J., Walter C.A., Fan W. et al.

Mol. Cell 1:783-793(1998) · UniProtKB (2)

Positionally cloned gene for a novel glomerular protein -- nephrin --is mutated in congenital nephrotic syndrome.

Kestilae M., Lenkkeri U., Maennikkoe M., Lamerdin J.E., McCready P., Putaala H., Ruotsalainen V., Morita T., Nissinen M., Herva R. et al.

Mol. Cell 1:575-582(1998) · UniProtKB (1)

Structure of the human amyloid-precursor-like protein gene APLP1 at 19q13.1.

Lenkkeri U., Kestila M., Lamerdin J.E., McCready P., Adamson A., Olsen A., Tryggvason K.

Hum. Genet. 102:192-196(1998) · UniProtKB (1)

The human XRCC9 gene corrects chromosomal instability and mutagen sensitivities in CHO UV40 cells.

Liu N., Lamerdin J.E., Tucker J.D., Zhou Z.-Q., Walter C.A., Albala J.S., Busch D.B., Thompson L.H.

Proc. Natl. Acad. Sci. U.S.A. 94:9232-9237(1997) · UniProtKB (1)

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.

Ophoff R.A., Terwindt G.M., Vergouwe M.N., van Eijk R., Oefner P.J., Hoffman S.M.G., Lamerdin J.E., Mohrenweiser H.W., Bulman D.E., Ferrari M. et al.

Cell 87:543-552(1996) · UniProtKB (1) · Mapped (1)

ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs.

Brookman K.W., Lamerdin J.E., Thelen M.P., Hwang M., Reardon J.T., Sancar A., Zhou Z.-Q., Walter C.A., Parris C.N., Thompson L.H.

Mol. Cell. Biol. 16:6553-6562(1996) · UniProtKB (1) · Mapped (2)

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)

Comparative analysis of a conserved zinc finger gene cluster on human chromosome 19q and mouse chromosome 7.

Shannon M., Ashworth L.K., Mucenski M.L., Lamerdin J.E., Branscomb E., Stubbs L.

Genomics 33:112-120(1996) · UniProtKB (4) · Mapped (16)

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)

Automated DNA sequencing and analysis of 106 kilobases from human chromosome 19q13.3.

Martin-Gallardo A., McCombie W.R., Gocayne J.D., Fitzgerald M.G., Wallace S., Lee B.M., Lamerdin J.E., Trapp S., Kelley J.M., Liu L.-I. et al.

Nat. Genet. 1:34-39(1992) · UniProtKB (1)

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