LitCoin-entities  

Documents (400) JSON TSV

source DB source ID text size updated at # proj. # Ann. updated_at
PubMed 16611040 Gene therapy for cystic fibrosis airway disease- is clinical success imminent? Cystic fibrosis (CF) was one of the first inherited disorders for which gene therapy was seriously considered as a realis 1.55 KB 2015-11-23 39 15 2021-12-05
PubMed 16720068 Possible neuroleptic malignant syndrome related to concomitant treatment with paroxetine and alprazolam. A 74-year-old man with depressive symptoms was admitted to a psychiatric hospital due to insomn 1.72 KB 2017-09-11 32 46 2021-12-05
PubMed 16801510 Drug-induced long QT syndrome in injection drug users receiving methadone: high frequency in hospitalized patients and risk factors. BACKGROUND: Drug-induced long QT syndrome is a serious adverse drug 1.87 KB 2015-11-23 23 35 2021-12-05
PubMed 16810074 Mechanisms of hypertension induced by nitric oxide (NO) deficiency: focus on venous function. Loss of endothelial cell-derived nitric oxide (NO) in hypertension is a hallmark of arterial dysfunction. 2.09 KB 2015-11-23 23 45 2021-12-05
PubMed 16820346 Atorvastatin prevented and reversed dexamethasone-induced hypertension in the rat. To assess the antioxidant effects of atorvastatin (atorva) on dexamethasone (dex)-induced hypertension, 60 male Sprag 1.09 KB 2015-11-23 25 37 2021-12-05
PubMed 16867021 Antipsychotic-like profile of thioperamide, a selective H3-receptor antagonist in mice. Experimental and clinical evidence points to a role of central histaminergic system in the pathogenesis of schiz 1.88 KB 2015-11-23 40 48 2021-12-05
PubMed 17006606 A polymorphism of C-to-T substitution at -31 IL1B is associated with the risk of advanced gastric adenocarcinoma in a Japanese population. Proinflammatory cytokine gene polymorphisms have been demonst 1.74 KB 2015-11-23 25 45 2021-12-05
PubMed 17033686 A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation. X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) a 1.62 KB 2017-09-11 33 30 2021-12-05
PubMed 17185386 Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1. We have previously reported a robust association between an alleli 1.58 KB 2015-11-23 27 17 2021-12-05
PubMed 17304550 Disruption of a synaptotagmin (SYT14) associated with neurodevelopmental abnormalities. We report cytogenetic and molecular studies of a de novo, apparently balanced t(1;3)(q32.1;q25.1) identified in 1.02 KB 2015-11-23 28 16 2021-12-05