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Structure of the alkalohyperthermophilic Archaeoglobus fulgidus lipase contains a unique C-terminal domain essential for long-chain substrate binding.

Chen C.K., Lee G.C., Ko T.P., Guo R.T., Huang L.M., Liu H.J., Ho Y.F., Shaw J.F., Wang A.H.

J. Mol. Biol. 390:672-685(2009) · Mapped (1)

Association study of promoter polymorphisms at the dopamine transporter gene in Attention Deficit Hyperactivity Disorder.

Xu X., Mill J., Sun B., Chen C.K., Huang Y.S., Wu Y.Y., Asherson P.

BMC Psychiatry 9:3-3(2009) · Mapped (4)

Trypanosoma cruzi CYP51 Inhibitor Derived from a Mycobacterium tuberculosis Screen Hit.

Chen C.K., Doyle P.S., Yermalitskaya L.V., Mackey Z.B., Ang K.K., McKerrow J.H., Podust L.M.

PLoS Negl Trop Dis 3:e372-e372(2009) · Mapped (1)

Psoriasis independently associated with hyperleptinemia contributing to metabolic syndrome.

Chen Y.J., Wu C.Y., Shen J.L., Chu S.Y., Chen C.K., Chang Y.T., Chen C.M.

Arch Dermatol 144:1571-1575(2008) · Mapped (5)

Role of LPA4/p2y9/GPR23 in negative regulation of cell motility.

Lee Z., Cheng C.T., Zhang H., Subler M.A., Wu J., Mukherjee A., Windle J.J., Chen C.K., Fang X.

Mol. Biol. Cell 19:5435-5445(2008) · Mapped (3)

Association of CT60 polymorphism of the CTLA4 gene with Graves' disease in Taiwanese children.

Tsai S.T., Huang C.Y., Lo F.S., Chang Y.T., Tanizawa T., Chen C.K., Wang Z.C., Liu H.F., Chu C.C., Lin M. et al.

J. Pediatr. Endocrinol. Metab. 21:665-672(2008) · Mapped (8)

Glycine N-methyltransferase is a favorable prognostic marker for human cholangiocarcinoma.

Huang Y.C., Chen M., Shyr Y.M., Su C.H., Chen C.K., Li A.F., Ho D.M., Chen Y.M.

J. Gastroenterol. Hepatol. 23:1384-1389(2008) · Mapped (1)

Genetic polymorphisms in the CD40 ligand gene and Kawasaki disease.

Huang F.Y., Chang T.Y., Chen M.R., Chiu N.C., Chi H., Lee H.C., Lin S.P., Chen C.K., Chan H.W., Chen W.F. et al.

J. Clin. Immunol. 28:405-410(2008) · Mapped (5)

Structures of a potent phenylalkyl bisphosphonate inhibitor bound to farnesyl and geranylgeranyl diphosphate synthases.

Cao R., Chen C.K., Guo R.T., Wang A.H., Oldfield E.

Proteins 73:431-439(2008) · Mapped (2)

Molecular architecture of Galphao and the structural basis for RGS16-mediated deactivation.

Slep K.C., Kercher M.A., Wieland T., Chen C.K., Simon M.I., Sigler P.B.

Proc. Natl. Acad. Sci. U.S.A. 105:6243-6248(2008) · Mapped (4)

Gbeta5 is required for normal light responses and morphology of retinal ON-bipolar cells.

Rao A., Dallman R., Henderson S., Chen C.K.

J. Neurosci. 27:14199-14204(2007) · Mapped (18)

Expression and localization of RGS9-2/G 5/R7BP complex in vivo is set by dynamic control of its constitutive degradation by cellular cysteine proteases.

Anderson G.R., Lujan R., Semenov A., Pravetoni M., Posokhova E.N., Song J.H., Uversky V., Chen C.K., Wickman K., Martemyanov K.A.

J. Neurosci. 27:14117-14127(2007) · Mapped (12)

Sphingosine-1-phosphate and endothelin-1 induce the expression of rgs16 protein in cardiac myocytes by transcriptional activation of the rgs16 gene.

Stuebe S., Wieland T., Kraemer E., Stritzky A., Schroeder D., Seekamp S., Vogt A., Chen C.K., Patten M.

Naunyn Schmiedebergs Arch. Pharmacol. 376:363-373(2008) · Mapped (5)

Analysis of association of clinical correlates and 5-HTTLPR polymorphism with suicidal behavior among Chinese methamphetamine abusers.

Chen C.K., Lin S.K., Huang M.C., Su L.W., Hsiao C.C., Chiang Y.L., Ree S.C., Chiang S.C., Liu H.C.

Psychiatry Clin. Neurosci. 61:479-486(2007) · Mapped (4)

Bisphosphonates target multiple sites in both cis- and trans-prenyltransferases.

Guo R.-T., Cao R., Liang P.-H., Ko T.-P., Chang T.-H., Hudock M.P., Jeng W.-Y., Chen C.K.-M., Zhang Y., Song Y. et al.

Proc. Natl. Acad. Sci. U.S.A. 104:10022-10027(2007) · UniProtKB (1) · Mapped (1)

CTLA-4 gene and susceptibility to human papillomavirus-16-associated cervical squamous cell carcinoma in Taiwanese women.

Su T.H., Chang T.Y., Lee Y.J., Chen C.K., Liu H.F., Chu C.C., Lin M., Wang P.T., Huang W.C., Chen T.C. et al.

Carcinogenesis 28:1237-1240(2007) · Mapped (8)

Association study between the monoamine oxidase A gene and attention deficit hyperactivity disorder in Taiwanese samples.

Xu X., Brookes K., Chen C.K., Huang Y.S., Wu Y.Y., Asherson P.

BMC Psychiatry 7:10-10(2007) · Mapped (9)

Transducin translocation in rods is triggered by saturation of the GTPase-activating complex.

Lobanova E.S., Finkelstein S., Song H., Tsang S.H., Chen C.K., Sokolov M., Skiba N.P., Arshavsky V.Y.

J. Neurosci. 27:1151-1160(2007) · Mapped (1)

Insulin-like growth factor-II (IGF-II), IGF-binding protein-3 (IGFBP-3), and IGFBP-4 in follicular fluid are associated with oocyte maturation and embryo development.

Wang T.H., Chang C.L., Wu H.M., Chiu Y.M., Chen C.K., Wang H.S.

Fertil. Steril. 86:1392-1401(2006) · Mapped (19)

Family-based association study between brain-derived neurotrophic factor gene polymorphisms and attention deficit hyperactivity disorder in UK and Taiwanese samples.

Xu X., Mill J., Zhou K., Brookes K., Chen C.K., Asherson P.

Am. J. Med. Genet. B Neuropsychiatr. Genet. 144B:83-86(2007) · Mapped (6)

RGS expression rate-limits recovery of rod photoresponses.

Krispel C.M., Chen D., Melling N., Chen Y.-J., Martemyanov K.A., Quillinan N., Arshavsky V.Y., Wensel T.G., Chen C.-K., Burns M.E.

Neuron 51:409-416(2006) · UniProtKB (3)

Association analysis of SOD2 variants with methamphetamine psychosis in Japanese and Taiwanese populations.

Nakamura K., Chen C.K., Sekine Y., Iwata Y., Anitha A., Loh e.l.-W., Takei N., Suzuki A., Kawai M., Takebayashi K. et al.

Hum. Genet. 120:243-252(2006) · Mapped (13)

Phototransduction in a transgenic mouse model of Nougaret night blindness.

Moussaif M., Rubin W.W., Kerov V., Reh R., Chen D., Lem J., Chen C.K., Hurley J.B., Burns M.E., Artemyev N.O.

J. Neurosci. 26:6863-6872(2006) · Mapped (1)

GAP-independent termination of photoreceptor light response by excess gamma subunit of the cGMP-phosphodiesterase.

Tsang S.H., Woodruff M.L., Chen C.K., Yamashita C.Y., Cilluffo M.C., Rao A.L., Farber D.B., Fain G.L.

J. Neurosci. 26:4472-4480(2006) · Mapped (8)

DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.

Zody M.C., Garber M., Adams D.J., Sharpe T., Harrow J., Lupski J.R., Nicholson C., Searle S.M., Wilming L., Young S.K. et al.

Nature 440:1045-1049(2006) · UniProtKB (913)

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