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1 - 25 of 69 results for author:"Chen T.T." in Literature citations

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[Association between mannose-binding lectin 2 gene and protein kinase C-beta 1 gene polymorphisms and type 2 diabetic macrovascular complications in northern Chinese Han population].

Zhang N.N., Yao L., Zhuang M.Q., Wang G.C., Chen T.T., Yang Y.J., Zhang J., Lv M., Jin L.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 29:709-714(2012) · Mapped (3)

ApoB-containing lipoproteins regulate angiogenesis by modulating expression of VEGF receptor 1.

Avraham-Davidi I., Ely Y., Pham V.N., Castranova D., Grunspan M., Malkinson G., Gibbs-Bar L., Mayseless O., Allmog G., Lo B. et al.

Nat. Med. 18:967-973(2012) · Mapped (52)

CCN2/connective tissue growth factor is essential for pericyte adhesion and endothelial basement membrane formation during angiogenesis.

Hall-Glenn F., De Young R.A., Huang B.L., van Handel B., Hofmann J.J., Chen T.T., Choi A., Ong J.R., Benya P.D., Mikkola H. et al.

PLoS ONE 7:e30562-e30562(2012) · Mapped (73)

VEGF internalization is not required for VEGFR-2 phosphorylation in bioengineered surfaces with covalently linked VEGF.

Anderson S.M., Shergill B., Barry Z.T., Manousiouthakis E., Chen T.T., Botvinick E., Platt M.O., Iruela-Arispe M.L., Segura T.

Integr Biol (Camb) 3:887-896(2011) · Mapped (9)

PML-RARalpha enhances constitutive autophagic activity through inhibiting the Akt/mTOR pathway.

Huang Y., Hou J.K., Chen T.T., Zhao X.Y., Yan Z.W., Zhang J., Yang J., Kogan S.C., Chen G.Q.

Autophagy 7:1132-1144(2011) · Mapped (20)

Activated NOTCH2 is overexpressed in hepatoblastomas: an immunohistochemical study.

Litten J.B., Chen T.T., Schultz R., Herman K., Comstock J., Schiffman J., Tomlinson G.E., Rakheja D.

Pediatr. Dev. Pathol. 14:378-383(2011) · Mapped (11)

Polymorphisms in CYP1A1 and ethnic-specific susceptibility to acute lymphoblastic leukemia in children.

Swinney R.M., Beuten J., Collier A.B., Chen T.T., Winick N.J., Pollock B.H., Tomlinson G.E.

Cancer Epidemiol. Biomarkers Prev. 20:1537-1542(2011) · Mapped (10)

Identification and functional characterization of rare mutations of the neuroligin-2 gene (NLGN2) associated with schizophrenia.

Sun C., Cheng M.C., Qin R., Liao D.L., Chen T.T., Koong F.J., Chen G., Chen C.H.

Hum. Mol. Genet. 20:3042-3051(2011) · Mapped (1)

[TfR2 mRNA expression in bone marrow mononuclear cells of children with hyperplastic anemia and its implications].

Chen T.T., Yuan L.X., Pan L.L., Ma Z.G., Gu L., Zhu Y.P., Gao J.

Zhongguo Shi Yan Xue Ye Xue Za Zhi 19:439-443(2011) · Mapped (2)

Impact of apolipoprotein A5 (APOA5) polymorphisms on serum triglyceride levels in schizophrenic patients under long-term atypical antipsychotic treatment.

Hong C.J., Chen T.T., Bai Y.M., Liou Y.J., Tsai S.J.

World J. Biol. Psychiatry 13:22-29(2012) · Mapped (3)

Knockout of Zn transporters Zip-1 and Zip-3 attenuates seizure-induced CA1 neurodegeneration.

Qian J., Xu K., Yoo J., Chen T.T., Andrews G., Noebels J.L.

J. Neurosci. 31:97-104(2011) · Mapped (5)

Association between HTR2C polymorphisms and metabolic syndrome in patients with schizophrenia treated with atypical antipsychotics.

Bai Y.M., Chen T.T., Liou Y.J., Hong C.J., Tsai S.J.

Schizophr. Res. 125:179-186(2011) · Mapped (2)

Analysis of genetic variations in the dopamine D1 receptor (DRD1) gene and antipsychotics-induced tardive dyskinesia in schizophrenia.

Lai I.C., Mo G.H., Chen M.L., Wang Y.C., Chen J.Y., Liao D.L., Bai Y.M., Lin C.C., Chen T.T., Liou Y.J.

Eur. J. Clin. Pharmacol. 67:383-388(2011) · Mapped (2)

Gene-gene interactions of the INSIG1 and INSIG2 in metabolic syndrome in schizophrenic patients treated with atypical antipsychotics.

Liou Y.J., Bai Y.M., Lin E., Chen J.Y., Chen T.T., Hong C.J., Tsai S.J.

Pharmacogenomics J. 12:54-61(2012) · Mapped (5)

Analysis of genetic variations in the human melatonin receptor (MTNR1A, MTNR1B) genes and antipsychotics-induced tardive dyskinesia in schizophrenia.

Lai I.C., Chen M.L., Wang Y.C., Chen J.Y., Liao D.L., Bai Y.M., Lin C.C., Chen T.T., Liou Y.J.

World J. Biol. Psychiatry 12:143-148(2011) · Mapped (5)

Resequencing of the vesicular glutamate transporter 2 gene (VGLUT2) reveals some rare genetic variants that may increase the genetic burden in schizophrenia.

Shen Y.C., Liao D.L., Lu C.L., Chen J.Y., Liou Y.J., Chen T.T., Chen C.H.

Schizophr. Res. 121:179-186(2010) · Mapped (2)

Hypoxia inducible factor-1 mediates expression of galectin-1: the potential role in migration/invasion of colorectal cancer cells.

Zhao X.Y., Chen T.T., Xia L., Guo M., Xu Y., Yue F., Jiang Y., Chen G.Q., Zhao K.W.

Carcinogenesis 31:1367-1375(2010) · Mapped (11)

Kv1.1 potassium channel deficiency reveals brain-driven cardiac dysfunction as a candidate mechanism for sudden unexplained death in epilepsy.

Glasscock E., Yoo J.W., Chen T.T., Klassen T.L., Noebels J.L.

J. Neurosci. 30:5167-5175(2010) · Mapped (4)

Dopamine receptor D2 gene is associated with weight gain in schizophrenic patients under long-term atypical antipsychotic treatment.

Hong C.J., Liou Y.J., Bai Y.M., Chen T.T., Wang Y.C., Tsai S.J.

Pharmacogenet. Genomics 20:359-366(2010) · Mapped (4)

[Expression of mitochondrial ferritin in K562 leukemic cell during ATRA-induced cell differentiation].

Sun L., Liao G., Gao J., Chen T.T., Pan L.L., Yuan L.X.

Sichuan Da Xue Xue Bao Yi Xue Ban 41:77-80, 2010:90-90(2010) · Mapped (1)

Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death.

Goldman A.M., Glasscock E., Yoo J., Chen T.T., Klassen T.L., Noebels J.L.

Sci Transl Med 1:2ra6-2ra6(2009) · Mapped (4)

CCAAT/enhancer binding protein beta2 is involved in growth hormone-regulated insulin-like growth factor-II gene expression in the liver of rainbow trout (Oncorhynchus mykiss).

Lo J.H., Chen T.T.

Endocrinology 151:2128-2139(2010) · UniProtKB (1)

Anchorage of VEGF to the extracellular matrix conveys differential signaling responses to endothelial cells.

Chen T.T., Luque A., Lee S., Anderson S.M., Segura T., Iruela-Arispe M.L.

J. Cell Biol. 188:595-609(2010) · Mapped (6)

[Expression of transferrin receptor 2 in mononuclear cells from children with acute leukemia].

Pan L.L., Gao J., Chen T.T., Ma Z.G., Guo X., Zhu Y.P., Li Q., Yuan L.X.

Sichuan Da Xue Xue Bao Yi Xue Ban 40:20-3, 2009:76-76(2009) · Mapped (2)

The coding-synonymous polymorphism rs1045280 (Ser280Ser) in beta-arrestin 2 (ARRB2) gene is associated with tardive dyskinesia in Chinese patients with schizophrenia.

Liou Y.J., Wang Y.C., Chen J.Y., Chen M.L., Chen T.T., Bai Y.M., Lin C.C., Liao D.L., Lai I.C.

Eur. J. Neurol. 15:1406-1408(2008) · Mapped (5)

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