Search results for "N8"

showing 7 items of 17 documents

Computational methodologies applied to Protein-Protein Interactions for molecular insights in Medicinal Chemistry

2021

In living systems, proteins usually team up into “molecular machinery” implementing several protein-to-protein physical contacts – or protein-protein interactions (PPIs) – to exert biological effects at both cellular and systems levels. Deregulations of protein-protein contacts have been associated with a huge number of diseases in a wide range of medical areas, such as oncology, cancer immunotherapy, infectious diseases, neurological disorders, heart failure, inflammation and oxidative stress. PPIs are very complex and usually characterised by specific shape, size and complementarity. The protein interfaces are generally large, broad and shallow, and frequently protein-protein contacts are…

InflammationComputer-Aided Drug DesignMolecular DynamicFactor HMolecular ModelingCOVID-19ACE2MUC1SpikeDrug AddictionHOXComputational Alanine ScanningC3bSettore CHIM/08 - Chimica FarmaceuticaProtein-Protein InteractionMolecular DockingComputational ChemistryNLRP3PBXCIN85RasGRF1RaCancer
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Evaluating resistance to Bt Toxin Cry1Ab by F-2 Screen in European populations of Ostrinia nubilalis (Lepidoptera: Crambidae)

2010

The large-scale cultivation of transgenic crops producing Bacillus thuringiensis (Bt) toxins have already lead to the evolution of Bt resistance in some pest populations targeted by these crops. We used the F2 screening method for further estimating the frequency of resistance alleles of the European corn borer, Ostrinia nubilalis (Hübner) (Lepidoptera: Crambidae), to Bt maize, Zea mays L., producing the Cry1Ab toxin. In France, Germany, and Italy, 784, 455, and 80 lines of European corn borer were screened for resistance to Mon810 maize, respectively. In Slovakia, 26 lines were screened for resistance to the Cry1Ab toxin. The cost of F2 screen performed in the four countries varied from U.…

MaleBt maizeresistance management[SDV]Life Sciences [q-bio]Drug ResistanceZea maysHemolysin ProteinsBacterial ProteinsGermanyAnimalsEuropean corn borer Bt maize Mon810 resistance management HDR strategyPest Control BiologicalBacillus thuringiensis ToxinsReproductionfungifood and beveragesHDR strategyEndotoxinsEuropeLepidopteraeuropean corn borerSettore AGR/11 - Entomologia Generale E ApplicataCosts and Cost AnalysisFemaleFranceMon810
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Sport as a vehicle for implementing corporate social responsibility: firms listed on the Warsaw and Moscow stock exchanges

2021

This paper provides a descriptive account of the extent to which firms listed on the Warsaw (WSE) and Moscow (MSE) Stock Exchanges use sport for their corporate social responsibility agendas. Drawing on institutional isomorphism, we deductively categorised CSR through sport cases based on the framework developed by Bason and Anagnostopoulos (2015). A total of 1317 documents were content-analysed, 442 from WSE firms and 875 from MSE firms. A total of 2501 CSR-through-sport initiatives were reported over the five-year period studied (2013-2017) in the WSE case and 2175 in the MSE case. Our results show that internationally listed firms are increasingly embracing sport for their CSR programs, …

Organizational Behavior and Human Resource ManagementStock exchangebusiness.industryCorporate social responsibilityAccountingBusinessBusiness and International ManagementN880EducationIsomorphism (sociology)European J. of International Management
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Neuronal ceroid-lipofuscinosis--late-infantile or Jansky-Bielschowsky type--revisited.

1996

Among the now eight genetic types of neuronal ceroid-lipofuscinoses (NCL), CLN1 to CLN8, CLN2 is considered classic late-infantile NCL. It was originally described by Janský in a family of eight children with four of them affected [Janský J (1908) Sborn Lek 13:165-196] and, subsequently, by Bielschowsky in a family of three children each of whom was affected, and, hence, termed Janský-Bielschowsky type of NCL. Earlier, archival studies of Bielschowsky's original post-mortem tissue blocks had documented accumulation of autofluorescent lipopigments with a curvilinear ultrastructure. In a subsequent study, described here, immunohistochemical absence of the CLN2-related lysosomal enzyme tripept…

Pathologymedicine.medical_specialtyFamilial disorderBiologyPathology and Forensic Medicine03 medical and health sciences0302 clinical medicineNeuronal Ceroid-LipofuscinosesmedicinePathologyHumansColoring Agents030304 developmental biologyNeurons0303 health sciencesParaffin EmbeddingGeneral NeuroscienceBrainHistory 20th Centurymedicine.diseaseMicroscopy ElectronMicroscopy FluorescenceCLN8Archival tissueNeuronal ceroid lipofuscinosisNeurology (clinical)030217 neurology & neurosurgeryBrain pathology (Zurich, Switzerland)
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The acetylation of spermidine catalyzed by P/CAF regulates its acetyltransferase activity versus histones

2010

Transcriptional regulation in eukaryotes occurs within a chromatin setting and is strongly inhibited by nucleosomal barriers imposed by histone proteins. Among the well-known covalent modifications of chromatin, the reversible acetylation of specific lysine residues of histones, catalyzed by several acetyltransferase and deacetylases, has been linked to many biological processes including transcriptional regulation. Indeed, many transcriptional coactivators possess histone acetyltransferase (HAT) activity (1). Functional interactions between HAT and polyamines have been previously reported. In particular, it has been shown that polyamines facilitate oligomerization of nucleosomal arrays in …

PolyamineN8-acetylspermidineSpermidineSettore BIO/10 - BiochimicaPCAF
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Commonalities and distinctions between two neurodevelopmental disorder subtypes associated with SCN2A and SCN8A variants and literature review.

2022

This study was aimed to analyze the commonalities and distinctions of voltage-gated sodium channels, Nav1.2, Nav1.6, in neurodevelopmental disorders. An observational study was performed including two patients with neurodevelopmental disorders. The demographic, electroclinical, genetic, and neuropsychological characteristics were analyzed and compared with each other and then with the subjects carrying the same genetic variants reported in the literature. The clinical features of one of them argued for autism spectrum disorder and developmental delay, the other for intellectual disability, diagnoses confirmed by the neuropsychological assessment. The first patient was a carrier of SCN2A (p.…

SCN8AEpilepsyNAV1.2 Voltage-Gated Sodium ChannelAutism Spectrum Disorderautism spectrum disordersObservational Studies as TopicPhenotypeNAV1.6 Voltage-Gated Sodium ChannelNeurodevelopmental DisordersIntellectual DisabilityHumansEEGwhole-exome sequencingSCN2AMolecular geneticsgenomic medicine
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CCDC 2118009: Experimental Crystal Structure Determination

2022

Related Article: Joschua Helmer, Olli J. Pakkanen, Chris Gendy, Alexander Hepp, Heikki M. Tuononen, Felicitas Lips|2022|Chem.Commun.|58|3549|doi:10.1039/D2CC00298A

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters9-bromo-N4N8-bis[dimethyl(phenyl)silyl]-N4N81-tris[26-bis(propan-2-yl)phenyl]-22-dimethyl-14a79-tetrahydro-2H-73-(metheno)silolo[1'2':34]trisileto[21-b][1235]azatrisilole-48-diamine toluene solvateExperimental 3D Coordinates
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