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1 - 25 of 51 results for author:"Patterson D."Drop in Literature Citations

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Multigene evidence for the placement of a heterotrophic amoeboid lineage Leukarachnion sp. among photosynthetic stramenopiles.

Grant J., Tekle Y.I., Anderson O.R., Patterson D.J., Katz L.A.

Protist 160:376-385(2009) · UniProtKB (7)

Associations of glutamate decarboxylase genes with initial sensitivity and age-at-onset of alcohol dependence in the Irish Affected Sib Pair Study of Alcohol Dependence.

Kuo P.H., Kalsi G., Prescott C.A., Hodgkinson C.A., Goldman D., Alexander J., van den Oord E.J., Chen X., Sullivan P.F., Patterson D.G. et al.

Drug Alcohol Depend 101:80-87(2009) · Mapped (13)

Mutations in the Chinese hamster ovary cell GART gene of de novo purine synthesis.

Knox A.J., Graham C., Bleskan J., Brodsky G., Patterson D.

Gene 429:23-30(2009) · UniProtKB (1)

Methylation-mediated downregulation of the B-cell translocation gene 3 (BTG3) in breast cancer cells.

Yu J., Zhang Y., Qi Z., Kurtycz D., Vacano G., Patterson D.

Gene Expr. 14:173-182(2008) · Mapped (3)

Mice transgenic for reduced folate carrier: an animal model of Down syndrome?

Hoger J., Patterson D., Hoger H., Shim K.S., Bubna-Littitz H., Lubec G.

Amino Acids 36:349-357(2009) · Mapped (6)

Association of ADH and ALDH genes with alcohol dependence in the Irish Affected Sib Pair Study of alcohol dependence (IASPSAD) sample.

Kuo P.H., Kalsi G., Prescott C.A., Hodgkinson C.A., Goldman D., van den Oord E.J., Alexander J., Jiang C., Sullivan P.F., Patterson D.G. et al.

Alcohol. Clin. Exp. Res. 32:785-795(2008) · Mapped (30)

Phylogenetic placement of diverse amoebae inferred from multigene analyses and assessment of clade stability within 'Amoebozoa' upon removal of varying rate classes of SSU-rDNA.

Tekle Y.I., Grant J., Anderson O.R., Nerad T.A., Cole J.C., Patterson D.J., Katz L.A.

Mol. Phylogenet. Evol. 47:339-352(2008) · UniProtKB (24)

Characterization of the essential activities of Saccharomyces cerevisiae Mtr4p, a 3'->5' helicase partner of the nuclear exosome.

Bernstein J., Patterson D.N., Wilson G.M., Toth E.A.

J. Biol. Chem. 283:4930-4942(2008) · Mapped (2)

A humanized mouse model for the reduced folate carrier.

Patterson D., Graham C., Cherian C., Matherly L.H.

Mol. Genet. Metab. 93:95-103(2008) · Mapped (10)

A multigene analysis of Corallomyxa tenera sp. nov. suggests its membership in a clade that includes Gromia, Haplosporidia and Foraminifera.

Tekle Y.I., Grant J., Cole J.C., Nerad T.A., Anderson O.R., Patterson D.J., Katz L.A.

Protist 158:457-472(2007) · UniProtKB (4)

Interaction between cytochrome P450 gene polymorphisms and serum organochlorine TEQ levels in the risk of endometriosis.

Tsuchiya M., Tsukino H., Iwasaki M., Sasaki H., Tanaka T., Katoh T., Patterson D.G. Jr., Turner W., Needham L., Tsugane S.

Mol. Hum. Reprod. 13:399-404(2007) · Mapped (16)

A complex rearrangement in GBE1 causes both perinatal hypoglycemic collapse and late-juvenile-onset neuromuscular degeneration in glycogen storage disease type IV of Norwegian forest cats.

Fyfe J.C., Kurzhals R.L., Hawkins M.G., Wang P., Yuhki N., Giger U., Van Winkle T.J., Haskins M.E., Patterson D.F., Henthorn P.S.

Mol. Genet. Metab. 90:383-392(2007) · UniProtKB (1)

Alcohol dependence is associated with the ZNF699 gene, a human locus related to Drosophila hangover, in the Irish Affected Sib Pair Study of Alcohol Dependence (IASPSAD) sample.

Riley B.P., Kalsi G., Kuo P.H., Vladimirov V., Thiselton D.L., Vittum J., Wormley B., Grotewiel M.S., Patterson D.G., Sullivan P.F. et al.

Mol. Psychiatry 11:1025-1031(2006) · Mapped (1)

Expression and shifting subcellular localization of the transcription factor, Foxd3, in embryonic and adult pancreas.

Perera H.K., Caldwell M.E., Hayes-Patterson D., Teng L., Peshavaria M., Jetton T.L., Labosky P.A.

Gene Expr. Patterns 6:971-977(2006) · Mapped (15)

The production of transgenic mice expressing human cystathionine beta-synthase to study Down syndrome.

Butler C., Knox A.J., Bowersox J., Forbes S., Patterson D.

Behav. Genet. 36:429-438(2006) · Mapped (6)

The keeshond defect in cardiac conotruncal development is oligogenic.

Werner P., Raducha M.G., Prociuk U., Ostrander E.A., Spielman R.S., Kirkness E.F., Patterson D.F., Henthorn P.S.

Hum. Genet. 116:368-377(2005) · UniProtKB (1)

CYP1A1 and CYP1B1 genotypes, haplotypes, and TCDD-induced gene expression in subjects from Seveso, Italy.

Landi M.T., Bergen A.W., Baccarelli A., Patterson D.G. Jr., Grassman J., Ter-Minassian M., Mocarelli P., Caporaso N., Masten S.A., Pesatori A.C. et al.

Toxicology 207:191-202(2005) · Mapped (6)

Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the equivalent mutant Bacillus subtilis ASL.

Sivendran S., Patterson D., Spiegel E., McGown I., Cowley D., Colman R.F.

J. Biol. Chem. 279:53789-53797(2004) · Mapped (6)

Evolutionary history of "early-diverging" eukaryotes: the excavate taxon Carpediemonas is a close relative of Giardia.

Simpson A.G., Roger A.J., Silberman J.D., Leipe D.D., Edgcomb V.P., Jermiin L.S., Patterson D.J., Sogin M.L.

Mol. Biol. Evol. 19:1782-1791(2002) · UniProtKB (2)

Canine cystinuria: polymorphism in the canine SLC3A1 gene and identification of a nonsense mutation in cystinuric Newfoundland dogs.

Henthorn P.S., Liu J., Gidalevich T., Fang J., Casal M.L., Patterson D.F., Giger U.

Hum. Genet. 107:295-303(2000) · UniProtKB (1) · Mapped (2)

Genetic mapping of a mouse modifier gene that can prevent ALS onset.

Kunst C.B., Messer L., Gordon J., Haines J., Patterson D.

Genomics 70:181-189(2000) · Mapped (14)

The DNA sequence of human chromosome 21.

Hattori M., Fujiyama A., Taylor T.D., Watanabe H., Yada T., Park H.-S., Toyoda A., Ishii K., Totoki Y., Choi D.-K. et al.

Nature 405:311-319(2000) · UniProtKB (506)

Human phosphoribosylformylglycinamide amidotransferase (FGARAT): regional mapping, complete coding sequence, isolation of a functional genomic clone, and DNA sequence analysis.

Patterson D., Bleskan J., Gardiner K., Bowersox J.

Gene 239:381-391(1999) · UniProtKB (1)

A missense mutation in canine C1C-1 causes recessive myotonia congenita in the dog.

Rhodes T.H., Vite C.H., Giger U., Patterson D.F., Fahlke C., George A.L. Jr.

FEBS Lett. 456:54-58(1999) · UniProtKB (1)

Molecular basis of feline beta-glucuronidase deficiency: an animal model of mucopolysaccharidosis VII.

Fyfe J.C., Kurzhals R.L., Lassaline M.E., Henthorn P.S., Alur P.R., Wang P., Wolfe J.H., Giger U., Haskins M.E., Patterson D.F. et al.

Genomics 58:121-128(1999) · UniProtKB (1)

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