Works matching IS 00071188 AND DT 2013 AND VI 168 AND IP 6

Results: 33

ARF6 and GASP-1 are post-endocytic sorting proteins selectively involved in the intracellular trafficking of dopamine D₂ receptors mediated by GRK and PKC in transfected cells.

Published in:

2013

By:

Cho, D I;
Zheng, M;
Min, C;
Kwon, K J;
Shin, C Y;
Choi, H K;
Kim, K M

Publication type:

journal article

Cannabidiolic acid prevents vomiting in Suncus murinus and nausea-induced behaviour in rats by enhancing 5-HT1A receptor activation.

Published in:

2013

By:

Bolognini, D;
Rock, E M;
Cluny, N L;
Cascio, M G;
Limebeer, C L;
Duncan, M;
Stott, C G;
Javid, F A;
Parker, L A;
Pertwee, R G

Publication type:

journal article

Sphingosine and FTY720 are potent inhibitors of the transient receptor potential melastatin 7 (TRPM7) channels.

Published in:

2013

By:

Qin, Xin;
Yue, Zhichao;
Sun, Baonan;
Yang, Wenzhong;
Xie, Jia;
Ni, Eric;
Feng, Yi;
Mahmood, Rafat;
Zhang, Yanhui;
Yue, Lixia

Publication type:

journal article

Deferasirox (ICL670A) effectively inhibits oesophageal cancer growth in vitro and in vivo.

Published in:

2013

By:

Ford, Sj;
Obeidy, P;
Lovejoy, Db;
Bedford, M;
Nichols, L;
Chadwick, C;
Tucker, O;
Lui, Gyl;
Kalinowski, Ds;
Jansson, Pj;
Iqbal, Th;
Alderson, D;
Richardson, Dr;
Tselepis, C;
Ford, S J;
Lovejoy, D B;
Lui, G Y L;
Kalinowski, D S;
Jansson, P J;
Iqbal, T H

Publication type:

journal article

Inhibition of endothelial cell Ca²⁺ entry and transient receptor potential channels by Sigma-1 receptor ligands.

Published in:

2013

By:

Amer, Mohamed S;
McKeown, Lynn;
Tumova, Sarka;
Liu, Ruifeng;
Seymour, Victoria Al;
Wilson, Lesley A;
Naylor, Jacqueline;
Greenhalgh, Katriona;
Hou, Bing;
Majeed, Yasser;
Turner, Paul;
Sedo, Alicia;
O'Regan, David J;
Li, Jing;
Bon, Robin S;
Porter, Karen E;
Beech, David J;
Seymour, Victoria A L

Publication type:

journal article

(S)-1-α-naphthylmethyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline (CKD712), promotes wound closure by producing VEGF through HO-1 induction in human dermal fibroblasts and mouse skin.

Published in:

2013

By:

Jang, Hwa Jin;
Tsoyi, Konstantin;
Kim, Young Min;
Park, Eun Jung;
Park, Sang Won;
Kim, Hye Jung;
Lee, Jae Heun;
Chang, Ki Churl

Publication type:

journal article

The sphingosine kinase inhibitor 2-(p-hyroxyanilino)-4-(p-chlorophenyl)thiazole reduces androgen receptor expression via an oxidative stress-dependent mechanism.

Published in:

2013

By:

Tonelli, Francesca;
Alossaimi, Manal;
Williamson, Leon;
Tate, Rothwelle J;
Watson, David G;
Chan, Edmond;
Bittman, Robert;
Pyne, Nigel J;
Pyne, Susan

Publication type:

journal article

Moxifloxacin modifies corneal fibroblast-to-myofibroblast differentiation.

Published in:

2013

By:

Chen, Tc;
Chang, Sw;
Wang, Ty;
Chen, T C;
Chang, S W;
Wang, T Y

Publication type:

journal article

Suppression of PU.1-linked TLR4 expression by cilostazol with decrease of cytokine production in macrophages from patients with rheumatoid arthritis.

Published in:

2013

By:

Park, Sy;
Lee, Sw;
Baek, Sh;
Lee, Cw;
Lee, Ws;
Rhim, By;
Hong, Kw;
Kim, Cd;
Park, S Y;
Lee, S W;
Baek, S H;
Lee, C W;
Lee, W S;
Rhim, B Y;
Hong, K W;
Kim, C D

Publication type:

journal article

(E)-2,4-bis(p-hydroxyphenyl)-2-butenal has an antiproliferative effect on NSCLC cells induced by p38 MAPK-mediated suppression of NF-κB and up-regulation of TNFRSF10B (DR5).

Published in:

2013

By:

Kollipara, Pushpa Saranya;
Jeong, Heon Sang;
Han, Sang Bae;
Hong, Jin Tae

Publication type:

journal article

Benzimidazolones enhance the function of epithelial Na⁺ transport.

Published in:

2013

By:

Laube, M;
Kimpel, Su;
Dietl, P;
Thome, Uh;
Wittekindt, Oh;
Kimpel, S U;
Thome, U H;
Wittekindt, O H

Publication type:

journal article

Activation and desensitization of TRPV1 channels in sensory neurons by the PPARα agonist palmitoylethanolamide.

Published in:

2013

By:

Ambrosino, Paolo;
Soldovieri, Maria Virginia;
Russo, Claudio;
Taglialatela, Maurizio

Publication type:

journal article

Suppression of PU.1-linked TLR4 expression by cilostazol with decrease of cytokine production in macrophages from patients with rheumatoid arthritis.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1401, doi. 10.1111/bph.12021

By:

Park, SY;
Lee, SW;
Baek, SH;
Lee, CW;
Lee, WS;
Rhim, BY;
Hong, KW;
Kim, CD

Publication type:

Article

Cannabidiolic acid prevents vomiting in Suncus murinus and nausea-induced behaviour in rats by enhancing 5- HT1A receptor activation.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1456, doi. 10.1111/bph.12043

By:

Bolognini, D;
Rock, EM;
Cluny, NL;
Cascio, MG;
Limebeer, CL;
Duncan, M;
Stott, CG;
Javid, FA;
Parker, LA;
Pertwee, RG

Publication type:

Article

ARF6 and GASP-1 are post-endocytic sorting proteins selectively involved in the intracellular trafficking of dopamine D2 receptors mediated by GRK and PKC in transfected cells.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1355, doi. 10.1111/bph.12025

By:

Cho, DI;
Zheng, M;
Min, C;
Kwon, KJ;
Shin, CY;
Choi, HK;
Kim, KM

Publication type:

Article

Activation and desensitization of TRPV1 channels in sensory neurons by the PPARα agonist palmitoylethanolamide.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1430, doi. 10.1111/bph.12029

By:

Ambrosino, Paolo;
Soldovieri, Maria Virginia;
Russo, Claudio;
Taglialatela, Maurizio

Publication type:

Article

Hydrogen water consumption prevents osteopenia in ovariectomized rats.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1412, doi. 10.1111/bph.12036

By:

Guo, Ji ‐ Dong;
Li, Li;
Shi, Ya ‐ Min;
Wang, Hua ‐ Dong;
Hou, Shu ‐ Xun

Publication type:

Article

Inhibition of CXCR3-mediated chemotaxis by the human chemokine receptor-like protein CCX-CKR.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1375, doi. 10.1111/bph.12042

By:

Vinet, J;
Zwam, M;
Dijkstra, IM;
Brouwer, N;
Weering, HRJ;
Watts, A;
Meijer, M;
Fokkens, MR;
Kannan, V;
Verzijl, D;
Vischer, HF;
Smit, MJ;
Leurs, R;
Biber, K;
Boddeke, HWGM

Publication type:

Article

( E)-2,4-bis( p-hydroxyphenyl)-2-butenal has an antiproliferative effect on NSCLC cells induced by p38 MAPK-mediated suppression of NF-κ B and up-regulation of TNFRSF10B (DR5).

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1471, doi. 10.1111/bph.12024

By:

Kollipara, Pushpa Saranya;
Jeong, Heon Sang;
Han, Sang Bae;
Hong, Jin Tae

Publication type:

Article

Iron chelation: a potential therapeutic strategy in oesophageal cancer.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1313, doi. 10.1111/bph.12093

By:

Keeler, BD;
Brookes, MJ

Publication type:

Article

( S)-1-α-naphthylmethyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline (CKD712), promotes wound closure by producing VEGF through HO-1 induction in human dermal fibroblasts and mouse skin.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1485, doi. 10.1111/bph.12031

By:

Jang, Hwa Jin;
Tsoyi, Konstantin;
Kim, Young Min;
Park, Eun Jung;
Park, Sang Won;
Kim, Hye Jung;
Lee, Jae Heun;
Chang, Ki Churl

Publication type:

Article

Issue Information.

Published in:: British Journal of Pharmacology, 2013, v. 168, n. 6, p. i, doi. 10.1111/j.1476-5381.2012.02153.x
Publication type:: Article

The sphingosine kinase inhibitor 2-( p-hyroxyanilino)-4-( p-chlorophenyl)thiazole reduces androgen receptor expression via an oxidative stress-dependent mechanism.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1497, doi. 10.1111/bph.12035

By:

Tonelli, Francesca;
Alossaimi, Manal;
Williamson, Leon;
Tate, Rothwelle J;
Watson, David G;
Chan, Edmond;
Bittman, Robert;
Pyne, Nigel J;
Pyne, Susan

Publication type:

Article

Pharmacological characterization of LPS and opioid interactions at the toll-like receptor 4.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1421, doi. 10.1111/bph.12028

By:

Stevens, CW;
Aravind, S;
Das, S;
Davis, RL

Publication type:

Article

Characterization of AQX-1125, a small-molecule SHIP1 activator Characterization of AQX-1125, a small-molecule SHIP1 activator: Part 1. Effects on inflammatory cell activation and chemotaxis in vitro and pharmacokinetic characterization in vivo.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1506, doi. 10.1111/bph.12039

By:

Stenton, Grant R;
Mackenzie, Lloyd F;
Tam, Patrick;
Cross, Jennifer L;
Harwig, Curtis;
Raymond, Jeffrey;
Toews, Judy;
Wu, Joyce;
Ogden, Nancy;
MacRury, Thomas;
Szabo, Csaba

Publication type:

Article

Inhibition of endothelial cell Ca2+ entry and transient receptor potential channels by Sigma-1 receptor ligands.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1445, doi. 10.1111/bph.12041

By:

Amer, Mohamed S;
McKeown, Lynn;
Tumova, Sarka;
Liu, Ruifeng;
Seymour, Victoria AL;
Wilson, Lesley A;
Naylor, Jacqueline;
Greenhalgh, Katriona;
Hou, Bing;
Majeed, Yasser;
Turner, Paul;
Sedo, Alicia;
O'Regan, David J;
Li, Jing;
Bon, Robin S;
Porter, Karen E;
Beech, David J

Publication type:

Article

Sphingosine and the transient receptor potential channel kinase(s).

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1291, doi. 10.1111/bph.12070

By:

Rohacs, Tibor

Publication type:

Article

Sphingosine and FTY720 are potent inhibitors of the transient receptor potential melastatin 7 ( TRPM7) channels.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1294, doi. 10.1111/bph.12012

By:

Qin, Xin;
Yue, Zhichao;
Sun, Baonan;
Yang, Wenzhong;
Xie, Jia;
Ni, Eric;
Feng, Yi;
Mahmood, Rafat;
Zhang, Yanhui;
Yue, Lixia

Publication type:

Article

Deferasirox ( ICL670A) effectively inhibits oesophageal cancer growth in vitro and in vivo.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1316, doi. 10.1111/bph.12045

By:

Ford, SJ;
Obeidy, P;
Lovejoy, DB;
Bedford, M;
Nichols, L;
Chadwick, C;
Tucker, O;
Lui, GYL;
Kalinowski, DS;
Jansson, PJ;
Iqbal, TH;
Alderson, D;
Richardson, DR;
Tselepis, C

Publication type:

Article

Benzimidazolones enhance the function of epithelial Na+ transport.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1329, doi. 10.1111/bph.12027

By:

Laube, M;
Kimpel, SU;
Dietl, P;
Thome, UH;
Wittekindt, OH

Publication type:

Article

Characterization of AQX-1125, a small-molecule SHIP1 activator Characterization of AQX-1125, a small-molecule SHIP1 activator: Part 2. Efficacy studies in allergic and pulmonary inflammation models in vivo.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1519, doi. 10.1111/bph.12038

By:

Stenton, Grant R;
Mackenzie, Lloyd F;
Tam, Patrick;
Cross, Jennifer L;
Harwig, Curtis;
Raymond, Jeffrey;
Toews, Judy;
Chernoff, David;
MacRury, Thomas;
Szabo, Csaba

Publication type:

Article

5- HT3 receptor antagonists ameliorate 5-fluorouracil-induced intestinal mucositis by suppression of apoptosis in murine intestinal crypt cells.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1388, doi. 10.1111/bph.12019

By:

Yasuda, M;
Kato, S;
Yamanaka, N;
Iimori, M;
Matsumoto, K;
Utsumi, D;
Kitahara, Y;
Amagase, K;
Horie, S;
Takeuchi, K

Publication type:

Article

Moxifloxacin modifies corneal fibroblast-to-myofibroblast differentiation.

Published in:

British Journal of Pharmacology, 2013, v. 168, n. 6, p. 1341, doi. 10.1111/bph.12015

By:

Chen, TC;
Chang, SW;
Wang, TY

Publication type:

Article

Works matching IS 00071188 AND DT 2013 AND VI 168 AND IP 6

ARF6 and GASP-1 are post-endocytic sorting proteins selectively involved in the intracellular trafficking of dopamine D₂ receptors mediated by GRK and PKC in transfected cells.

Cannabidiolic acid prevents vomiting in Suncus murinus and nausea-induced behaviour in rats by enhancing 5-HT1A receptor activation.

Sphingosine and FTY720 are potent inhibitors of the transient receptor potential melastatin 7 (TRPM7) channels.

Deferasirox (ICL670A) effectively inhibits oesophageal cancer growth in vitro and in vivo.

Inhibition of endothelial cell Ca²⁺ entry and transient receptor potential channels by Sigma-1 receptor ligands.

(S)-1-α-naphthylmethyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline (CKD712), promotes wound closure by producing VEGF through HO-1 induction in human dermal fibroblasts and mouse skin.

The sphingosine kinase inhibitor 2-(p-hyroxyanilino)-4-(p-chlorophenyl)thiazole reduces androgen receptor expression via an oxidative stress-dependent mechanism.

Moxifloxacin modifies corneal fibroblast-to-myofibroblast differentiation.

Suppression of PU.1-linked TLR4 expression by cilostazol with decrease of cytokine production in macrophages from patients with rheumatoid arthritis.

(E)-2,4-bis(p-hydroxyphenyl)-2-butenal has an antiproliferative effect on NSCLC cells induced by p38 MAPK-mediated suppression of NF-κB and up-regulation of TNFRSF10B (DR5).

Benzimidazolones enhance the function of epithelial Na⁺ transport.

Activation and desensitization of TRPV1 channels in sensory neurons by the PPARα agonist palmitoylethanolamide.

Suppression of PU.1-linked TLR4 expression by cilostazol with decrease of cytokine production in macrophages from patients with rheumatoid arthritis.

Cannabidiolic acid prevents vomiting in Suncus murinus and nausea-induced behaviour in rats by enhancing 5- HT<sub>1A</sub> receptor activation.

ARF6 and GASP-1 are post-endocytic sorting proteins selectively involved in the intracellular trafficking of dopamine D<sub>2</sub> receptors mediated by GRK and PKC in transfected cells.

Activation and desensitization of TRPV1 channels in sensory neurons by the PPARα agonist palmitoylethanolamide.

Hydrogen water consumption prevents osteopenia in ovariectomized rats.

Inhibition of CXCR3-mediated chemotaxis by the human chemokine receptor-like protein CCX-CKR.

( E)-2,4-bis( p-hydroxyphenyl)-2-butenal has an antiproliferative effect on NSCLC cells induced by p38 MAPK-mediated suppression of NF-κ B and up-regulation of TNFRSF10B (DR5).

Iron chelation: a potential therapeutic strategy in oesophageal cancer.

( S)-1-α-naphthylmethyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline (CKD712), promotes wound closure by producing VEGF through HO-1 induction in human dermal fibroblasts and mouse skin.

Issue Information.

The sphingosine kinase inhibitor 2-( p-hyroxyanilino)-4-( p-chlorophenyl)thiazole reduces androgen receptor expression via an oxidative stress-dependent mechanism.

Pharmacological characterization of LPS and opioid interactions at the toll-like receptor 4.

Characterization of AQX-1125, a small-molecule SHIP1 activator Characterization of AQX-1125, a small-molecule SHIP1 activator: Part 1. Effects on inflammatory cell activation and chemotaxis in vitro and pharmacokinetic characterization in vivo.

Inhibition of endothelial cell Ca<sup>2+</sup> entry and transient receptor potential channels by Sigma-1 receptor ligands.

Sphingosine and the transient receptor potential channel kinase(s).

Sphingosine and FTY720 are potent inhibitors of the transient receptor potential melastatin 7 ( TRPM7) channels.

Deferasirox ( ICL670A) effectively inhibits oesophageal cancer growth in vitro and in vivo.

Benzimidazolones enhance the function of epithelial Na<sup>+</sup> transport.

Characterization of AQX-1125, a small-molecule SHIP1 activator Characterization of AQX-1125, a small-molecule SHIP1 activator: Part 2. Efficacy studies in allergic and pulmonary inflammation models in vivo.

5- HT<sub>3</sub> receptor antagonists ameliorate 5-fluorouracil-induced intestinal mucositis by suppression of apoptosis in murine intestinal crypt cells.

Moxifloxacin modifies corneal fibroblast-to-myofibroblast differentiation.