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Cutting edge: Dab2 is a FOXP3 target gene required for regulatory T cell function.

Jain N., Nguyen H., Friedline R.H., Malhotra N., Brehm M., Koyanagi M., Bix M., Cooper J.A., Chambers C.A., Kang J.

J. Immunol. 183:4192-4196(2009) · Mapped (8)

Identification and Isolation of an Azoreductase from Enterococcus faecium.

Macwana S.R., Punj S., Cooper J., Schwenk E., John G.H.

Curr Issues Mol Biol 12:43-48(2009) · UniProtKB (1)

Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource.

Dendrou C.A., Plagnol V., Fung E., Yang J.H., Downes K., Cooper J.D., Nutland S., Coleman G., Himsworth M., Hardy M. et al.

Nat. Genet. 41:1011-1015(2009) · Mapped (7)

Molecular correlates of axonal and synaptic pathology in mouse models of Batten disease.

Kielar C., Wishart T.M., Palmer A., Dihanich S., Wong A.M., Macauley S.L., Chan C.H., Sands M.S., Pearce D.A., Cooper J.D. et al.

Hum. Mol. Genet. 18:4066-4080(2009) · Mapped (10)

Quantitative proteomics identifies a Dab2/integrin module regulating cell migration.

Teckchandani A., Toida N., Goodchild J., Henderson C., Watts J., Wollscheid B., Cooper J.A.

J. Cell Biol. 186:99-111(2009) · Mapped (3)

Light-dependent and light-independent protochlorophyllide oxidoreductases in the chromatically adapting cyanobacterium Fremyella diplosiphon UTEX 481.

Shui J., Saunders E., Needleman R., Nappi M., Cooper J., Hall L., Kehoe D., Stowe-Evans E.

Plant Cell Physiol. 50:1507-1521(2009) · UniProtKB (1)

Relationship between alpha synuclein phosphorylation, proteasomal inhibition and cell death: relevance to Parkinson's disease pathogenesis.

Chau K.Y., Ching H.L., Schapira A.H., Cooper J.M.

J. Neurochem. 110:1005-1013(2009) · Mapped (1)

Cerebellar pathology and motor deficits in the palmitoyl protein thioesterase 1-deficient mouse.

Macauley S.L., Wozniak D.F., Kielar C., Tan Y., Cooper J.D., Sands M.S.

Exp. Neurol. 217:124-135(2009) · Mapped (10)

Function of dynein in budding yeast: mitotic spindle positioning in a polarized cell.

Moore J.K., Stuchell-Brereton M.D., Cooper J.A.

Cell Motil. Cytoskeleton 66:546-555(2009) · Mapped (5)

The mating-specific Galpha interacts with a kinesin-14 and regulates pheromone-induced nuclear migration in budding yeast.

Zaichick S.V., Metodiev M.V., Nelson S.A., Durbrovskyi O., Draper E., Cooper J.A., Stone D.E.

Mol. Biol. Cell 20:2820-2830(2009) · Mapped (4)

Progressive thalamocortical neuron loss in Cln5 deficient mice: Distinct effects in Finnish variant late infantile NCL.

Schantz C., Kielar C., Hansen S.N., Pontikis C.C., Alexander N.A., Kopra O., Jalanko A., Cooper J.D.

Neurobiol. Dis. 34:308-319(2009) · Mapped (2)

Association between the adiponectin promoter rs266729 gene variant and oxidative stress in patients with diabetes mellitus.

Prior S.L., Gable D.R., Cooper J.A., Bain S.C., Hurel S.J., Humphries S.E., Stephens J.W.

Eur. Heart J. 30:1263-1269(2009) · Mapped (3)

Neurodegeneration mutations in dynactin impair dynein-dependent nuclear migration.

Moore J.K., Sept D., Cooper J.A.

Proc. Natl. Acad. Sci. U.S.A. 106:5147-5152(2009) · Mapped (16)

Silencing of PINK1 expression affects mitochondrial DNA and oxidative phosphorylation in dopaminergic cells.

Gegg M.E., Cooper J.M., Schapira A.H., Taanman J.W.

PLoS ONE 4:e4756-e4756(2009) · Mapped (1)

The Ndc80 kinetochore complex forms load-bearing attachments to dynamic microtubule tips via biased diffusion.

Powers A.F., Franck A.D., Gestaut D.R., Cooper J., Gracyzk B., Wei R.R., Wordeman L., Davis T.N., Asbury C.L.

Cell 136:865-875(2009) · Mapped (4)

Cerebellar defects in a mouse model of juvenile neuronal ceroid lipofuscinosis.

Weimer J.M., Benedict J.W., Getty A.L., Pontikis C.C., Lim M.J., Cooper J.D., Pearce D.A.

Brain Res. 1266:93-107(2009) · Mapped (5)

Structure of human porphobilinogen deaminase at 2.8 A: the molecular basis of acute intermittent porphyria.

Gill R., Kolstoe S.E., Mohammed F., Al D-Bass A., Mosely J.E., Sarwar M., Cooper J.B., Wood S.P., Shoolingin-Jordan P.M.

Biochem. J. 420:17-25(2009) · Mapped (4)

Actin and endocytosis: mechanisms and phylogeny.

Galletta B.J., Cooper J.A.

Curr. Opin. Cell Biol. 21:20-27(2009) · Mapped (15)

Restriction of Src activity by Cullin-5.

Laszlo G.S., Cooper J.A.

Curr. Biol. 19:157-162(2009) · Mapped (9)

IL2RA genetic heterogeneity in multiple sclerosis and type 1 diabetes susceptibility and soluble interleukin-2 receptor production.

International Multiple Sclerosis Genetics Consortium

PLoS Genet. 5:e1000322-e1000322(2009) · Mapped (7)

Analysis of 17 autoimmune disease-associated variants in type 1 diabetes identifies 6q23/TNFAIP3 as a susceptibility locus.

Fung E.Y., Smyth D.J., Howson J.M., Cooper J.D., Walker N.M., Stevens H., Wicker L.S., Todd J.A.

Genes Immun. 10:188-191(2009) · Mapped (64)

Shared and distinct genetic variants in type 1 diabetes and celiac disease.

Smyth D.J., Plagnol V., Walker N.M., Cooper J.D., Downes K., Yang J.H.M., Howson J.M.M., Stevens H., McManus R., Wijmenga C. et al.

N. Engl. J. Med. 359:2767-2777(2008) · UniProtKB (1) · Mapped (95)

A kinesin-13 mutant catalytically depolymerizes microtubules in ADP.

Wagenbach M., Domnitz S., Wordeman L., Cooper J.

J. Cell Biol. 183:617-623(2008) · UniProtKB (1) · Mapped (8)

Dual functions of Dab1 during brain development.

Feng L., Cooper J.A.

Mol. Cell. Biol. 29:324-332(2009) · Mapped (29)

ANGPTL4 E40K and T266M: effects on plasma triglyceride and HDL levels, postprandial responses, and CHD risk.

EARSII Consortium

Arterioscler. Thromb. Vasc. Biol. 28:2319-2325(2008) · Mapped (3)

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