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Extent of foetal exposure to maternal elexacaftor/tezacaftor/ivacaftor during pregnancy

British journal of pharmacology, 2024-08, Vol.181 (15), p.2413-2428

2024

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Targeting MDR‐1 gene expression, BAX/BCL2, caspase‐3, and Ki‐67 by nanoencapsulated imatinib and hesperidin to enhance anticancer activity and ameliorate cardiotoxicity

Fundamental & clinical pharmacology, 2020-08, Vol.34 (4), p.458-475

2020

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Design, synthesis and pharmacophoric model building of new 3‐alkoxymethyl/3‐phenyl indole‐2‐carboxamides with potential antiproliferative activity

Chemical biology & drug design, 2017-07, Vol.90 (1), p.64-82

2017

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miR‐1 is increased in pulmonary hypertension and downregulates Kv1.5 channels in rat pulmonary arteries

The Journal of physiology, 2019-02, Vol.597 (4), p.1185-1197

2019

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Chronic drug‐induced effects on contractile motion properties and cardiac biomarkers in human induced pluripotent stem cell‐derived cardiomyocytes

British journal of pharmacology, 2017-11, Vol.174 (21), p.3766-3779

2017

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Pharmaco‐toxicological effects of the novel third‐generation fluorinate synthetic cannabinoids, 5F‐ADBINACA, AB‐FUBINACA, and STS‐135 in mice. In vitro and in vivo studies

Human psychopharmacology, 2017-05, Vol.32 (3), p.n/a

2017

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Duocarmycin Analogues Target Aldehyde Dehydrogenase 1 in Lung Cancer Cells

Angewandte Chemie (International ed.), 2012-03, Vol.51 (12), p.2874-2877

2012

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Synthesis, structure-activity relationship studies and biological evaluation of novel 2,5-disubstituted indole derivatives as anticancer agents

Chemical biology & drug design, 2016-11, Vol.88 (5), p.766-778

2016

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Phthalocyanine-Polyamine Conjugates as pH-Controlled Photosensitizers for Photodynamic Therapy

Chemistry : a European journal, 2010-04, Vol.16 (16), p.4777-4783

2010

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CrossTalk proposal: The mouse SuHx model is a good model of pulmonary arterial hypertension

The Journal of physiology, 2019-02, Vol.597 (4), p.975-977

2019

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CB1 receptor-mediated signaling underlies the hippocampal synaptic, learning, and memory deficits following treatment with JWH-081, a new component of spice/K2 preparations

Hippocampus, 2014-02, Vol.24 (2), p.178-188

2014

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Evaluating tumor metastatic potential by imaging intratumoral acidosis via pH‐activatable near‐infrared fluorescent probe

International journal of cancer, 2015-02, Vol.136 (4), p.E107-E116

2015

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CrossTalk opposing view: The mouse SuHx model is not a good model of pulmonary arterial hypertension

The Journal of physiology, 2019-02, Vol.597 (4), p.979-981

Vitali, Sally H.

2019

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Toxicity of imine-iminium dyes and pigments: electron transfer, radicals, oxidative stress and other physiological effects

Journal of applied toxicology, 2014-08, Vol.34 (8), p.825-834

2014

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The phosphatidylinositol 3‐kinases (PI3K) inhibitor GS‐1101 synergistically potentiates histone deacetylase inhibitor‐induced proliferation inhibition and apoptosis through the inactivation of PI3K and extracellular signal‐regulated kinase pathways

British journal of haematology, 2013-10, Vol.163 (1), p.72-80

2013

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Retrospective evaluation of toceranib phosphate (Palladia®) toxicity in cats

Veterinary & comparative oncology, 2017-09, Vol.15 (3), p.710-717

2017

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Rationally Designed Less Toxic SPD-304 Analogs and Preliminary Evaluation of Their TNF Inhibitory Effects

Archiv der Pharmazie (Weinheim), 2014-11, Vol.347 (11), p.798-805

2014

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Statins and fenofibrate affect skeletal muscle chloride conductance in rats by differently impairing ClC‐1 channel regulation and expression

British journal of pharmacology, 2009-04, Vol.156 (8), p.1206-1215

2009

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Chloride channels as tools for developing selective insecticides

Archives of insect biochemistry and physiology, 2003-12, Vol.54 (4), p.145-156

Bloomquist, Jeffrey R

2003

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The potential of enzastaurin to enhance platelet aggregation and growth factor secretion: implications for cancer cell survival

Journal of thrombosis and haemostasis, 2015-08, Vol.13 (8), p.1514-1520

2015

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Involvement of organic anion transporting polypeptides in the toxicity of hydrophilic pravastatin and lipophilic fluvastatin in rat skeletal myofibres

British journal of pharmacology, 2008-08, Vol.154 (7), p.1482-1490

2008

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Carcinogenicity and hormone studies with the tissue-selective estrogen receptor modulator bazadoxifene

Journal of cellular physiology, 2013-04, Vol.228 (4), p.724-733

2013

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Antibody-Directed Enzyme Prodrug Therapy: A Promising Approach for a Selective Treatment of Cancer Based on Prodrugs and Monoclonal Antibodies

Chemical biology & drug design, 2009-09, Vol.74 (3), p.205-211

2009

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Anticonvulsant Activity of Novel 1-(Substituted Benzylidene)-4-(1-(Morpholino/Piperidino Methyl)-2,3-Dioxoindolin-5-yl) Semicarbazide Derivatives in Mice and Rats Acute Seizure Models

Chemical biology & drug design, 2012-10, Vol.80 (4), p.524-532

2012

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5-Nitro-5'hydroxy-indirubin-3'oxime is a novel inducer of somatic cell transdifferentiation

Archiv der Pharmazie (Weinheim), 2014-11, Vol.347 (11), p.806-818

2014

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Extent of foetal exposure to maternal elexacaftor/tezacaftor/ivacaftor during pregnancy

Targeting MDR‐1 gene expression, BAX/BCL2, caspase‐3, and Ki‐67 by nanoencapsulated imatinib and hesperidin to enhance anticancer activity and ameliorate cardiotoxicity

Design, synthesis and pharmacophoric model building of new 3‐alkoxymethyl/3‐phenyl indole‐2‐carboxamides with potential antiproliferative activity

miR‐1 is increased in pulmonary hypertension and downregulates Kv1.5 channels in rat pulmonary arteries

Chronic drug‐induced effects on contractile motion properties and cardiac biomarkers in human induced pluripotent stem cell‐derived cardiomyocytes

Pharmaco‐toxicological effects of the novel third‐generation fluorinate synthetic cannabinoids, 5F‐ADBINACA, AB‐FUBINACA, and STS‐135 in mice. In vitro and in vivo studies

Duocarmycin Analogues Target Aldehyde Dehydrogenase 1 in Lung Cancer Cells

Synthesis, structure-activity relationship studies and biological evaluation of novel 2,5-disubstituted indole derivatives as anticancer agents

Phthalocyanine-Polyamine Conjugates as pH-Controlled Photosensitizers for Photodynamic Therapy

CrossTalk proposal: The mouse SuHx model is a good model of pulmonary arterial hypertension

CB1 receptor-mediated signaling underlies the hippocampal synaptic, learning, and memory deficits following treatment with JWH-081, a new component of spice/K2 preparations

Evaluating tumor metastatic potential by imaging intratumoral acidosis via pH‐activatable near‐infrared fluorescent probe

CrossTalk opposing view: The mouse SuHx model is not a good model of pulmonary arterial hypertension

Toxicity of imine-iminium dyes and pigments: electron transfer, radicals, oxidative stress and other physiological effects

The phosphatidylinositol 3‐kinases (PI3K) inhibitor GS‐1101 synergistically potentiates histone deacetylase inhibitor‐induced proliferation inhibition and apoptosis through the inactivation of PI3K and extracellular signal‐regulated kinase pathways

Retrospective evaluation of toceranib phosphate (Palladia®) toxicity in cats

Rationally Designed Less Toxic SPD-304 Analogs and Preliminary Evaluation of Their TNF Inhibitory Effects

Statins and fenofibrate affect skeletal muscle chloride conductance in rats by differently impairing ClC‐1 channel regulation and expression

Chloride channels as tools for developing selective insecticides

The potential of enzastaurin to enhance platelet aggregation and growth factor secretion: implications for cancer cell survival

Involvement of organic anion transporting polypeptides in the toxicity of hydrophilic pravastatin and lipophilic fluvastatin in rat skeletal myofibres

Carcinogenicity and hormone studies with the tissue-selective estrogen receptor modulator bazadoxifene

Antibody-Directed Enzyme Prodrug Therapy: A Promising Approach for a Selective Treatment of Cancer Based on Prodrugs and Monoclonal Antibodies

Anticonvulsant Activity of Novel 1-(Substituted Benzylidene)-4-(1-(Morpholino/Piperidino Methyl)-2,3-Dioxoindolin-5-yl) Semicarbazide Derivatives in Mice and Rats Acute Seizure Models

5-Nitro-5'hydroxy-indirubin-3'oxime is a novel inducer of somatic cell transdifferentiation

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