Search Results - "Legos, J J"
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Dabrafenib plus trametinib versus dabrafenib monotherapy in patients with metastatic BRAF V600E/K-mutant melanoma: long-term survival and safety analysis of a phase 3 study
Published in Annals of oncology (01-07-2017)“…Previous analysis of COMBI-d (NCT01584648) demonstrated improved progression-free survival (PFS) and overall survival (OS) with combination dabrafenib and…”
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Comparison of dabrafenib and trametinib combination therapy with vemurafenib monotherapy on health-related quality of life in patients with unresectable or metastatic cutaneous BRAF Val600-mutation-positive melanoma (COMBI-v): results of a phase 3, open-label, randomised trial
Published in The lancet oncology (01-10-2015)“…Summary Background In the COMBI-v trial, patients with previously untreated BRAF Val600Glu or Val600Lys mutant unresectable or metastatic melanoma who were…”
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Dabrafenib plus trametinib versus dabrafenib monotherapy in patients with metastatic BRAF V600E/K-mutant melanoma: long-term survival and safety analysis of a phase 3 study
Published in ANNALS OF ONCOLOGY (01-11-2019)Get full text
Journal Article Publication -
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Caspase 3 Activation Is Essential for Neuroprotection in Preconditioning
Published in Proceedings of the National Academy of Sciences - PNAS (21-01-2003)“…Sublethal insults can induce tolerance to subsequent stressors in neurons. As cell death activators such as ROS generation and decreased ATP can initiate…”
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SB 239063, a second-generation p38 mitogen-activated protein kinase inhibitor, reduces brain injury and neurological deficits in cerebral focal ischemia
Published in The Journal of pharmacology and experimental therapeutics (01-02-2001)“…The stress-activated mitogen-activated protein kinase (MAPK) p38 has been linked to the production of inflammatory cytokines/mediators/inflammation and…”
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Inhibition of p38 mitogen-activated protein kinase provides neuroprotection in cerebral focal ischemia
Published in Medicinal research reviews (01-03-2001)“…Mitogen‐activated protein kinases (MAPKs) are involved in many cellular processes. The stress‐activated MAPK, p38, has been linked to inflammatory cytokine…”
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3301 Two year estimate of overall survival in COMBI-v, a randomized, open-label, phase III study comparing the combination of dabrafenib (D) and trametinib (T) with vemurafenib (Vem) as first-line therapy in patients (pts) with unresectable or metastatic BRAF V600E/K mutation-positive cutaneous melanoma
Published in European journal of cancer (1990) (01-09-2015)Get full text
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Association of body-mass index and outcomes in patients with metastatic melanoma treated with targeted therapy, immunotherapy, or chemotherapy: a retrospective, multicohort analysis
Published in The lancet oncology (01-03-2018)“…Obesity has been linked to increased mortality in several cancer types; however, the relation between obesity and survival outcomes in metastatic melanoma is…”
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Quantitative changes in interleukin proteins following focal stroke in the rat
Published in Neuroscience letters (24-03-2000)“…The aim of the present study was to quantitate the temporal changes in protein concentration for interleukin (IL)-1α, IL-1β, IL-1ra, and IL-6 from 1 h to 15…”
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Dabrafenib and trametinib versus dabrafenib and placebo for Val600 BRAF-mutant melanoma: a multicentre, double-blind, phase 3 randomised controlled trial
Published in The Lancet (British edition) (01-08-2015)“…Summary Background Previously, a study of ours showed that the combination of dabrafenib and trametinib improves progression-free survival compared with…”
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Three-year pooled analysis of factors associated with clinical outcomes across dabrafenib and trametinib combination therapy phase 3 randomised trials
Published in European journal of cancer (1990) (01-09-2017)“…Understanding predictors of long-term benefit with currently available melanoma therapies is the key for optimising individualised treatments. A prior pooled…”
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SB 239063, a novel p38 inhibitor, attenuates early neuronal injury following ischemia
Published in Brain research (16-02-2001)“…The aim of the present study was to evaluate p38 MAPK activation following focal stroke and determine whether SB 239063, a novel second generation p38…”
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Stroke Genomics: Approaches to Identify, Validate, and Understand Ischemic Stroke Gene Expression
Published in Journal of Cerebral Blood Flow & Metabolism (01-07-2001)“…Sequencing of the human genome is nearing completion and biologists, molecular biologists, and bioinformatics specialists have teamed up to develop global…”
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Pharmacological interventions for stroke: failures and future
Published in Expert opinion on investigational drugs (01-05-2002)“…Given the few options currently available for patients following ischaemic stroke, the recent disappointing failures of several large-scale Phase III clinical…”
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Nonpeptide tachykinin receptor antagonists. III. SB 235375, a low central nervous system-penetrant, potent and selective neurokinin-3 receptor antagonist, inhibits citric acid-induced cough and airways hyper-reactivity in guinea pigs
Published in The Journal of pharmacology and experimental therapeutics (01-01-2002)“…In this report the in vitro and in vivo pharmacological and pharmacokinetic profile of…”
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BRAF(V600) Inhibitor GSK2118436 Targeted Inhibition of Mutant BRAF in Cancer Patients Does Not Impair Overall Immune Competency
Published in Clinical cancer research (15-04-2012)“…An intact immune system likely contributes to the outcome of treatment and may be important for clearance of drug-resistant tumor cells and for prevention of…”
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Expression of PEP-19 inhibits apoptosis in PC12 cells
Published in Neuroreport (27-11-2000)“…PEP-19 is a calmodulin-regulatory protein found specifically within neurons, though cellular functions of this protein have not been determined. In an effort…”
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Nonpeptide tachykinin receptor antagonists. II. Pharmacological and pharmacokinetic profile of SB-222200, a central nervous system penetrant, potent and selective NK-3 receptor antagonist
Published in The Journal of pharmacology and experimental therapeutics (01-10-2000)“…The pharmacological and pharmacokinetic profile of SB-222200 [(S)-(-)-N-(alpha-ethylbenzyl)-3-methyl-2-phenylquinoline-4-car boxami de], a human NK-3 receptor…”
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Inhibition of phosphodiesterase type 4 decreases stress-induced defecation in rats and mice
Published in Pharmacology (01-01-2008)“…Phosphodiesterase type 4 (PDE4) has been previously shown to regulate colonic contractile activity in vitro. In this study, the effects of PDE4 inhibition were…”
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