Skip Header

 

1 - 25 of 57 results for author:"Flint J."Drop in Literature Citations

Customize display Download...

Page of 3 | Next »

Understanding how diverse beta-mannanases recognize heterogeneous substrates.

Tailford L.E., Ducros V.M., Flint J.E., Roberts S.M., Morland C., Zechel D.L., Smith N., Bjornvad M.E., Borchert T.V., Wilson K.S. et al.

Biochemistry 48:7009-7018(2009) · Mapped (3)

The active site of a carbohydrate esterase displays divergent catalytic and noncatalytic binding functions.

Montanier C., Money V.A., Pires V.M., Flint J.E., Pinheiro B.A., Goyal A., Prates J.A., Izumi A., Stalbrand H., Morland C. et al.

PLoS Biol. 7:e71-e71(2009) · Mapped (3)

Two common single nucleotide polymorphisms in the gene encoding beta-carotene 15,15'-monoxygenase alter beta-carotene metabolism in female volunteers.

Leung W.C., Hessel S., Meplan C., Flint J., Oberhauser V., Tourniaire F., Hesketh J.E., von Lintig J., Lietz G.

FASEB J. 23:1041-1053(2009) · Mapped (2)

Gene X environment interactions at the serotonin transporter locus.

Munafo M.R., Durrant C., Lewis G., Flint J.

Biol. Psychiatry 65:211-219(2009) · Mapped (4)

5-HTTLPR genotype and anxiety-related personality traits: a meta-analysis and new data.

Munafo M.R., Freimer N.B., Ng W., Ophoff R., Veijola J., Miettunen J., Jarvelin M.R., Taanila A., Flint J.

Am. J. Med. Genet. B Neuropsychiatr. Genet. 150B:271-281(2009) · Mapped (4)

Engineering hyperthermostability into a GH11 xylanase is mediated by subtle changes to protein structure.

Dumon C., Varvak A., Wall M.A., Flint J.E., Lewis R.J., Lakey J.H., Morland C., Luginbuhl P., Healey S., Todaro T. et al.

J. Biol. Chem. 283:22557-22564(2008) · UniProtKB (1)

Crystal structure of a cellulosomal family 3 carbohydrate esterase from Clostridium thermocellum provides insights into the mechanism of substrate recognition.

Correia M.A., Prates J.A., Bras J., Fontes C.M., Newman J.A., Lewis R.J., Gilbert H.J., Flint J.E.

J. Mol. Biol. 379:64-72(2008) · Mapped (2)

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women.

Shifman S., Johannesson M., Bronstein M., Chen S.X., Collier D.A., Craddock N.J., Kendler K.S., Li T., O'Donovan M., O'Neill F.A. et al.

PLoS Genet. 4:e28-e28(2008) · Mapped (6)

Understanding the structural basis for substrate and inhibitor recognition in eukaryotic GH11 xylanases.

Vardakou M., Dumon C., Murray J.W., Christakopoulos P., Weiner D.P., Juge N., Lewis R.J., Gilbert H.J., Flint J.E.

J. Mol. Biol. 375:1293-1305(2008) · Mapped (1)

Neuregulin 1 genotype and schizophrenia.

Munafo M.R., Attwood A.S., Flint J.

Schizophr Bull 34:9-12(2008) · Mapped (26)

Nuclear factor-kappaB p65 facilitates longitudinal bone growth by inducing growth plate chondrocyte proliferation and differentiation and by preventing apoptosis.

Wu S., Flint J.K., Rezvani G., De Luca F.

J. Biol. Chem. 282:33698-33706(2007) · Mapped (1)

A whole genome association study of neuroticism using DNA pooling.

Shifman S., Bhomra A., Smiley S., Wray N.R., James M.R., Martin N.G., Hettema J.M., An S.S., Neale M.C., van den Oord E.J. et al.

Mol. Psychiatry 13:302-312(2008) · Mapped (4)

Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A).

Poirier K., Keays D.A., Francis F., Saillour Y., Bahi N., Manouvrier S., Fallet-Bianco C., Pasquier L., Toutain A., Tuy F.P. et al.

Hum. Mutat. 28:1055-1064(2007) · UniProtKB (1) · Mapped (5)

Association of the dopamine D4 receptor (DRD4) gene and approach-related personality traits: meta-analysis and new data.

Munafo M.R., Yalcin B., Willis-Owen S.A., Flint J.

Biol. Psychiatry 63:197-206(2008) · Mapped (59)

Association of the DRD2 gene Taq1A polymorphism and alcoholism: a meta-analysis of case-control studies and evidence of publication bias.

Munafo M.R., Matheson I.J., Flint J.

Mol. Psychiatry 12:454-461(2007) · Mapped (6)

Mapping regulatory variants for the serotonin transporter gene based on allelic expression imbalance.

Martin J., Cleak J., Willis-Owen S.A., Flint J., Shifman S.

Mol. Psychiatry 12:421-422(2007) · Mapped (4)

Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans.

Keays D.A., Tian G., Poirier K., Huang G.J., Siebold C., Cleak J., Oliver P.L., Fray M., Harvey R.J., Molnar Z. et al.

Cell 128:45-57(2007) · Mapped (6)

The brain-derived neurotrophic factor Val66Met polymorphism is associated with sense of coherence in a non-clinical community sample of 7335 adults.

Surtees P.G., Wainwright N.W., Willis-Owen S.A., Sandhu M.S., Luben R., Day N.E., Flint J.

J Psychiatr Res 41:707-710(2007) · Mapped (6)

Genome-wide genetic association of complex traits in heterogeneous stock mice.

Valdar W., Solberg L.C., Gauguier D., Burnett S., Klenerman P., Cookson W.O., Taylor M.S., Rawlins J.N., Mott R., Flint J.

Nat. Genet. 38:879-887(2006) · Mapped (10)

Probing the structural basis for the difference in thermostability displayed by family 10 xylanases.

Xie H., Flint J., Vardakou M., Lakey J.H., Lewis R.J., Gilbert H.J., Dumon C.

J. Mol. Biol. 360:157-167(2006) · Mapped (1)

Rgs 2 gene polymorphisms as modulators of anxiety in humans?

Leygraf A., Hohoff C., Freitag C., Willis-Owen S.A., Krakowitzky P., Fritze J., Franke P., Bandelow B., Fimmers R., Flint J. et al.

J Neural Transm 113:1921-1925(2006) · Mapped (2)

Association of the NRG1 gene and schizophrenia: a meta-analysis.

Munafo M.R., Thiselton D.L., Clark T.G., Flint J.

Mol. Psychiatry 11:539-546(2006) · Mapped (26)

No association between the BDNF Val66Met polymorphism and mood status in a non-clinical community sample of 7389 older adults.

Surtees P.G., Wainwright N.W., Willis-Owen S.A., Sandhu M.S., Luben R., Day N.E., Flint J.

J Psychiatr Res 41:404-409(2007) · Mapped (6)

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans.

Aitman T.J., Dong R., Vyse T.J., Norsworthy P.J., Johnson M.D., Smith J., Mangion J., Roberton-Lowe C., Marshall A.J., Petretto E. et al.

Nature 439:851-855(2006) · UniProtKB (1) · Mapped (4)

DCNP1: a novel candidate gene for major depression.

Willis-Owen S.A.G., Shifman S., Copley R.R., Flint J.

Mol. Psychiatry 11:121-122(2006) · UniProtKB (1)

Page of 3 | Next »