![]() ; Brunner, Martin ![]() in Journal of Experimental Education (2016), 85 Detailed reference viewed: 97 (1 UL)![]() Roelens, Nathalie ![]() ![]() in Il lavoro culturale (2016) Detailed reference viewed: 103 (12 UL)![]() Te Heesen, Kerstin ![]() Speeches/Talks (2016) Detailed reference viewed: 15 (0 UL)![]() Te Heesen, Kerstin ![]() Speeches/Talks (2016) Detailed reference viewed: 20 (0 UL)![]() Te Heesen, Kerstin ![]() Scientific Conference (2016) Detailed reference viewed: 14 (0 UL)![]() ; ; et al in Neurobiology of Aging (2016), 39 Presenilin-associated rhomboid-like (PARL), a serine protease located in the inner mitochondrial membrane, has been shown to genetically interact and process PTEN-induced putative kinase a protein known ... [more ▼] Presenilin-associated rhomboid-like (PARL), a serine protease located in the inner mitochondrial membrane, has been shown to genetically interact and process PTEN-induced putative kinase a protein known for its critical role in mitochondrial homeostasis and early-onset forms of Parkinson’s disease (PD). The identification of a PD-associated variant in the PARL gene (p.Ser77Asn) led us to assess the relevance of PARL for PD pathogenesis using a mutation screening of the coding sequences and adjacent intronic sequences. We investigated 3 single nucleotide polymorphisms (rs3792589, rs13091, and rs3732581), a synonymous base substitution (Leu79Leu) and the previously described p.Ser77Asn mutation, which were subsequently screened in more than 2000 patients and controls. Not detecting the p.Ser77Asn mutation in our cohort, nor a robust association between variations in the PARL gene and PD, the role of disease causing genetic variants in the PARL gene could not be further substantiated in our samples. Our findings indicate that PARL mutations are a rare cause of PD and genetic variants are neither strong nor common risk factors in PD. [less ▲] Detailed reference viewed: 222 (30 UL)![]() Fridgen, Gilbert ![]() ![]() in Applied Energy (2016), 180 Detailed reference viewed: 74 (8 UL)![]() Mersch, Sam ![]() in Philologica Jassyensia (2016), 23 Detailed reference viewed: 136 (1 UL)![]() Gabbay, Dov M. ![]() in Journal of Logic and Computation (2016), 26(1), 247--292 Detailed reference viewed: 126 (2 UL)![]() Gabbay, Dov M. ![]() in Journal of Logic and Computation (2016), 26(4), 1065--1147 Detailed reference viewed: 137 (2 UL)![]() ; Gabbay, Dov M. ![]() in Journal of Logic and Computation (2016), 26(4), 1051--1053 Detailed reference viewed: 144 (1 UL)![]() Cebotari, Victor ![]() in Journal of Ethnic and Migration Studies (2016), 42(5), 834856 Detailed reference viewed: 48 (0 UL)![]() Cebotari, Victor ![]() in Identities: Global Studies in Culture and Power (2016), 23(6), 648-666 While the topic of identity of ethnic minorities abounds in theoretical insights, most discussion is still clustered around the civic?ethnic divide while assuming conclusions with limited empirical ... [more ▼] While the topic of identity of ethnic minorities abounds in theoretical insights, most discussion is still clustered around the civic?ethnic divide while assuming conclusions with limited empirical evidence. By contrast, this article uses a four-category typology of identity that considers both in-group and out-group attachments to address hypotheses about competing identities and about factors influencing minorities to adopt one identity type over others. Based on unique data evidence of 12 ethnic minorities in Central and Eastern Europe, this study concludes that the ?hybrid? identity, rather than the literature-assumed ?ethnic? identity, tops the identification preference of minorities, although there are differences in levels and patterns when controlling for various covariates. The choice of identity depends on the socialisation process, the economic status, the perceived discrimination and intergroup tensions, reflecting variations in the system of values common to a region with complex ethnic dynamics. [less ▲] Detailed reference viewed: 91 (1 UL)![]() Cebotari, Victor ![]() in International Journal of Educational Development (2016), 51(November), 96107 Detailed reference viewed: 48 (2 UL)![]() Derian, Maxime ![]() in IFRATH (2016) Cette recherche étudie la frontière entre réparation et augmentation du corps humain par la technologie au travers de l’étude de l’agénésie de membre, c’est à dire de l’absence congénitale d’un ou ... [more ▼] Cette recherche étudie la frontière entre réparation et augmentation du corps humain par la technologie au travers de l’étude de l’agénésie de membre, c’est à dire de l’absence congénitale d’un ou plusieurs membre(s), segment(s) de membre(s) ou extrémité(s). L’analyse porte sur les enjeux sociologiques et psychologiques liés à la vulnérabilité somatique et à la suppléance prothétique par l’étude de ce cas particulier de malformation de naissance. [less ▲] Detailed reference viewed: 90 (3 UL)![]() ; ; et al in Cellulose (2016) We report the ability of cellulose to support cells without the use of matrix ligands on the surface of the material, thus creating a two-component system for tissue engineering of cells and materials ... [more ▼] We report the ability of cellulose to support cells without the use of matrix ligands on the surface of the material, thus creating a two-component system for tissue engineering of cells and materials. Sheets of bacterial cellulose, grown from a culture medium containing Acetobacter organism were chemically modified with glycidyltrimethylammonium chloride or by oxidation with sodium hypochlorite in the presence of sodium bromide and 2,2,6,6-tetramethylpipiridine 1-oxyl radical to introduce a positive, or negative, charge, respectively. This modification process did not degrade the mechanical properties of the bulk material, but grafting of a positively charged moiety to the cellulose surface (cationic cellulose) increased cell attachment by 70 compared to unmodified cellulose, while negatively charged, oxidised cellulose films (anionic cellulose), showed low levels of cell attachment comparable to those seen for unmodified cellulose. Only a minimal level of cationic surface derivitisation (ca 3 degree of substitution) was required for increased cell attachment and no mediating proteins were required. Cell adhesion studies exhibited the same trends as the attachment studies, while the mean cell area and aspect ratio was highest on the cationic surfaces. Overall, we demonstrated the utility of positively charged bacterial cellulose in tissue engineering in the absence of proteins for cell attachment. [less ▲] Detailed reference viewed: 86 (1 UL)![]() ; Mettus, Denis ![]() in Journal of Alloys and Compounds (2016), 661 Detailed reference viewed: 145 (11 UL)![]() ; ; Neyses, Ludwig ![]() in Pharmacology and Therapeutics (2016), 159 The incidence of hypertension, the major modifiable risk factor for cardiovascular disease, is increasing. Thus, there is a pressing need for the development of new and more effective strategies to ... [more ▼] The incidence of hypertension, the major modifiable risk factor for cardiovascular disease, is increasing. Thus, there is a pressing need for the development of new and more effective strategies to prevent and treat hypertension. Development of these relies on a continued evolution of our understanding of the mechanisms which control blood pressure (BP). Resistance arteries are important in the regulation of total peripheral resistance and BP; changes in their structure and function are strongly associated with hypertension. Anti-hypertensives which both reduce BP and reverse changes in resistance arterial structure reduce cardiovascular risk more than therapies which reduce BP alone. Hence, identification of novel potential vascular targets which modify BP is important. Hypertension is a multifactorial disorder which may include a genetic component. Genome wide association studies have identified ATP2B1, encoding the calcium pump plasma membrane calcium ATPase 1 (PMCA1), as having a strong association with BP and hypertension. Knockdown or reduced PMCA1 expression in mice has confirmed a physiological role for PMCA1 in BP and resistance arterial regulation. Altered expression or inhibition of PMCA4 has also been shown to modulate these parameters. The mechanisms whereby PMCA1 and 4 can modulate vascular function remain to be fully elucidated but may involve regulation of intracellular calcium homeostasis and/or comprise a structural role. However, clear physiological links between PMCA and BP, coupled with experimental studies directly linking PMCA1 and 4 to changes in BP and arterial function, suggest that they may be important targets for the development of new pharmacological modulators of BP. [less ▲] Detailed reference viewed: 146 (3 UL)![]() ; Titov, Ivan ![]() in Journal of Alloys and Compounds (2016), 677 Detailed reference viewed: 141 (2 UL)![]() Tommasini, Matteo ![]() in Journal of Geometry and Physics (2016), 108 Detailed reference viewed: 94 (1 UL) |
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