全部文献期刊学位论文会议报纸专利标准年鉴图书|学者科研项目
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作者:Giuseppe Novelli , Leonardo Palombi
来源:[J].European Journal of Clinical Pharmacology(IF 2.741), 2017, Vol.73 (10), pp.1253-1259Springer
摘要:Nevirapine (NVP) is used in developing countries as first-line treatment of HIV infection. Unfortunately, its use is associated with common serious adverse drug reactions, such as liver toxicity and the most severe and rare Stevens-Johnson syndrome (SJS) and toxic epidermal necro...
作者:... Cinzia Ciccacci , Giuseppe Novelli , Paola Borgiani
来源:[J].Immunologic Research(IF 2.963), 2017, Vol.65 (4), pp.811-827Springer
摘要:MicroRNAs (miRNAs) are small non-coding RNA molecules that negatively regulate the expression of multiple protein-encoding genes at the post-transcriptional level. MicroRNAs are involved in different pathways, such as cellular proliferation and differentiation, signal transductio...
作者:... Francesco Garaci , Giuseppe Novelli , Paolo Sbraccia
来源:[J].BMC Medical Genetics(IF 2.536), 2016, Vol.17 (1)Springer
摘要:Abstract(#br) Background(#br)Bilateral posterior periventricular nodular heterotopia PNH is a complex malformation of cortical development with imaging features distinguishing it from classic bilateral PNH associated with filamin ( FLNA ) mutations. It distinctively consists of v...
作者:... Francesco Romeo , Giuseppe Novelli , Alberico Luigi Catapano
来源:[J].PLoS ONE(IF 3.73), 2018, Vol.7 (2)DOAJ
摘要:The lectin-like oxidised LDL receptor-1 (OLR1) gene encodes a scavenger receptor implicated in the pathogenesis of atherosclerosis. Although functional roles have been suggested for two variants, epidemiological studies on OLR1 have been inconsistent.We tested the association bet...
作者:... Francesco Romeo , Giuseppe Novelli , Francesca Amati
来源:[J].PLoS ONE(IF 3.73), 2019, Vol.14 (5)DOAJ
摘要:Coronary artery disease (CAD) and acute myocardial infarction (AMI) are the leading causes of death worldwide. Since only a subset of CAD patients develops myocardial infarction, it is likely that unique factors predispose to AMI. Circulating microRNAs represent diagnostic p...
作者:... Stefano Gambardella , Federica Sangiuolo , Giuseppe Novelli
来源:[J].BMC Medical Genetics(IF 2.536), 2011, Vol.12 (1)Springer
摘要:Abstract(#br) Background(#br)Treacher Collins syndrome (TCS) is one of the most severe autosomal dominant congenital disorders of craniofacial development and shows variable phenotypic expression. TCS is extremely rare, occurring with an incidence of 1 in 50.000 live births. The ...

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