Search results for "M2"

showing 10 items of 256 documents

Development of a Novel Object Detection System Based on Synthetic Data Generated from Unreal Game Engine

2022

This paper presents a novel approach to training a real-world object detection system based on synthetic data utilizing state-of-the-art technologies. Training an object detection system can be challenging and time-consuming as machine learning requires substantial volumes of training data with associated metadata. Synthetic data can solve this by providing unlimited desired training data with automatic generation. However, the main challenge is creating a balanced dataset that closes the reality gap and generalizes well when deployed in the real world. A state-of-the-art game engine, Unreal Engine 4, was used to approach the challenge of generating a photorealistic dataset for deep learnin…

Fluid Flow and Transfer ProcessesVDP::Teknologi: 500Process Chemistry and TechnologyGeneral Engineeringcomputer vision; deep learning; domain randomization; object detection; NDDS; PyTorch; sim2real; synthetic data; Unreal Engine; YOLOv5General Materials ScienceVDP::Matematikk og Naturvitenskap: 400InstrumentationComputer Science ApplicationsApplied Sciences
researchProduct

Chapter 17 Muscarinic receptors and cell signalling

1996

Publisher Summary Cells have developed signal transduction mechanisms in order to communicate with the cell exterior. Acetylcholine as an external signal is recognized by nicotinic and muscarinic receptors. This chapter presents various muscarinic receptors belonging to the superfamily of G protein-coupled receptors consisting of seven transmembrane (TM) helices tightly packed in a ring-like structure and arranged in a counter-clockwise fashion. Agonist binding leads to a conformational change of the receptor, thereby activating associated G proteins. Muscarinic stimulation of G proteins leads to the activation or inhibition of ion channels, such as K + and Ca 2+ channels, the activation of…

G proteinHeterotrimeric G proteinMuscarinic acetylcholine receptor M5Muscarinic acetylcholine receptor M2Muscarinic acetylcholine receptor M1BiologyG protein-gated ion channelRhodopsin-like receptorsG protein-coupled receptorCell biology
researchProduct

The transmembrane Bax inhibitor motif (TMBIM) containing protein family: Tissue expression, intracellular localization and effects on the ER CA2+-fil…

2015

Abstract Bax inhibitor-1 (BI-1) is an evolutionarily conserved pH-dependent Ca2+ leak channel in the endoplasmic reticulum and the founding member of a family of six highly hydrophobic mammalian proteins named transmembrane BAX inhibitor motif containing (TMBIM) 1-6 with BI-1 being TMBIM6. Here we compared the structure, subcellular localization, tissue expression and the effect on the cellular Ca2+ homeostasis of all family members side by side. We found that all TMBIM proteins possess the di-aspartyl pH sensor responsible for pH sensing identified in TMBIM6 and its bacterial homologue BsYetJ. TMBIM1-3 and TMBIM4-6 represent two phylogenetically distinct groups that are localized in the Go…

GHITMGAAPProtein familyEndoplasmic reticulumCell BiologyBiologyGolgi apparatusSubcellular localizationFAIM2Transmembrane proteinGHITMCell biologyTransmembrane domainsymbols.namesakeMICS1BiochemistryMembrane proteinGRINAsymbolsRECS1Molecular BiologyBiochimica et Biophysica Acta (BBA) - Molecular Cell Research
researchProduct

THE SHAPLEY-SOLIDARITY VALUE FOR GAMES WITH A COALITION STRUCTURE

2013

A value for games with a coalition structure is introduced, where the rules guiding cooperation among the members of the same coalition are different from the interaction rules among coalitions. In particular, players inside a coalition exhibit a greater degree of solidarity than they are willing to use with players outside their coalition. The Shapley value is therefore used to compute the aggregate payoffs for the coalitions, and the solidarity value to obtain the payoffs for the players inside each coalition.

General Computer ScienceCoalitional value Shapley value Owen value Solidarity value C71ComputingMilieux_PERSONALCOMPUTINGMathematicsofComputing_GENERALStructure (category theory)TheoryofComputation_GENERALComputingMethodologies_ARTIFICIALINTELLIGENCEShapley valueSolidarityjel:M2MicroeconomicsCore (game theory)Value (economics)jel:C0Economicsjel:D5Statistics Probability and UncertaintyBusiness and International Managementjel:B4jel:C6jel:D7Mathematical economicsjel:C7International Game Theory Review
researchProduct

Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy

2002

Nemaline myopathy is a clinically and genetically heterogeneous muscle disorder. In the nebulin gene we have detected a number of autosomal recessive mutations. Both autosomal dominant and recessive mutations have been detected in the genes for alpha -actin and alpha -tropomyosin 3. A recessive mutation causing nemaline myopathy among the Old Order Amish has recently been identified in the gene for slow skeletal muscle troponin T. As linkage studies had shown that at least one further gene exists for nemaline myopathy, we investigated another tropomyosin gene expressed in skeletal muscle, the beta -tropomyosin 2 gene. Screening 66 unrelated patients, using single strand conformation polymor…

Genetic MarkersMaleGenetic LinkageProtein ConformationBiopsyMolecular Sequence DataMutation MissenseTropomyosinmacromolecular substancesMuscle disorderMyopathies NemalineTPM203 medical and health sciencesNebulin0302 clinical medicineNemaline myopathymedicineAnimalsHumansAmino Acid SequenceMuscle SkeletalNemaline bodiesPolymorphism Single-Stranded ConformationalGenetics (clinical)DNA Primers030304 developmental biologyGenetics0303 health sciencesSequence Homology Amino AcidbiologyReverse Transcriptase Polymerase Chain Reactionmusculoskeletal systemmedicine.diseaseMolecular biologyTropomyosinCongenital myopathyPedigree3. Good healthHaplotypesNeurologyMutationPediatrics Perinatology and Child Healthbiology.proteinFemaleNeurology (clinical)Sequence Alignment030217 neurology & neurosurgeryCentral core diseaseNeuromuscular Disorders
researchProduct

Heterodimerization of Two Pathological Mutants Enhances the Activity of Human Phosphomannomutase2

2015

The most frequent disorder of glycosylation is due to mutations in the gene encoding phosphomannomutase2 (PMM2-CDG). For this disease, which is autosomal and recessive, there is no cure at present. Most patients are composite heterozygous and carry one allele encoding an inactive mutant, R141H, and one encoding a hypomorphic mutant. Phosphomannomutase2 is a dimer. We reproduced composite heterozygosity in vitro by mixing R141H either with the wild type protein or the most common hypomorphic mutant F119L and compared the quaternary structure, the activity and the stability of the heterodimeric enzymes. We demonstrated that the activity of R141H/F119L heterodimers in vitro, which reproduces t…

Genetics and Molecular Biology (all)HeterozygoteProtein StructureGlycosylationMutantlcsh:MedicineGlucose-6-PhosphateBiologymedicine.disease_causeBiochemistryQuaternaryCongenital Disorders of GlycosylationProtein structuremedicineAlleles; Congenital Disorders of Glycosylation; Dimerization; Glucose-6-Phosphate; Glycosylation; Heterozygote; Humans; Mutation; Phosphorylation; Phosphotransferases (Phosphomutases); Protein Structure Quaternary; Agricultural and Biological Sciences (all); Biochemistry Genetics and Molecular Biology (all); Medicine (all)HumansPhosphorylationAlleleProtein Structure Quaternarylcsh:ScienceGeneAllelesMutationMultidisciplinaryMedicine (all)lcsh:RWild typeMolecular biologyEnzyme structureProteostasisAgricultural and Biological Sciences (all)heterodimresPhosphotransferases (Phosphomutases)Mutationlcsh:QCDG-PMM2DimerizationResearch ArticlePLOS ONE
researchProduct

Languages associated with saturated formations of groups

2013

International audience; In a previous paper, the authors have shown that Eilenberg's variety theorem can be extended to more general structures, called formations. In this paper, we give a general method to describe the languages corresponding to saturated formations of groups, which are widely studied in group theory. We recover in this way a number of known results about the languages corresponding to the classes of nilpotent groups, soluble groups and supersoluble groups. Our method also applies to new examples, like the class of groups having a Sylow tower.; Dans un article précédent, les auteurs avaient montré comment étendre le théorème des variétés d'Eilenberg à des structures plus g…

Group formationGeneral MathematicsFinite monoid[INFO.INFO-OH]Computer Science [cs]/Other [cs.OH]0102 computer and information sciences01 natural sciencesregular languageRegular languageÁlgebra0101 mathematicsValenciaMathematicsFinite groupbiologyApplied Mathematics010102 general mathematicsACM: F.: Theory of Computation/F.4: MATHEMATICAL LOGIC AND FORMAL LANGUAGES/F.4.3: Formal LanguagesRegular languagebiology.organism_classificationAlgebra010201 computation theory & mathematicsMSC 68Q70 20D10 20F17 20M25finite groupsaturated formationformationsFinite automata
researchProduct

Macrophage MerTK promotes profibrogenic cross-talk with hepatic stellate cells via soluble mediators

2022

Background & aims: Activation of Kupffer cells and recruitment of monocytes are key events in fibrogenesis. These cells release soluble mediators which induce the activation of hepatic stellate cells (HSCs), the main fibrogenic cell type within the liver. Mer tyrosine kinase (MerTK) signaling regulates multiple processes in macrophages and has been implicated in the pathogenesis of non-alcoholic steatohepatitis-related fibrosis. In this study, we explored if MerTK activation in macrophages influences the profibrogenic phenotype of HSCs. Methods: Macrophages were derived from THP-1 cells or differentiated from peripheral blood monocytes towards MerTK+/CD206+/CD163+/CD209- macrophages. Th…

HepatologyCM conditioned medium ECM extracellular matrix Gas-6 Gas-6 growth arrest-specific gene 6 HSC(s) hepatic stellate cells KC(s) Kupffer cell(s) M-CSF macrophage colony-stimulating factor M2c-like macrophages MerTK Myeloid-epithelial-reproductive tyrosine kinase NAFLD non-alcoholic fatty liver disease NASH NASH non-alcoholic steatohepatitis PMA phorbol 12-myristate 13-acetate TGFβ1 transforming growth factor-β1 THP-1 TIMP1 tissue inhibitor of metalloproteinase 1 VEGF-A vascular endothelial growth factor-A liver fibrosis siRNA small-interfering RNAGas-6; liver fibrosis; M2c-like macrophages; NASH; THP-1GastroenterologyInternal MedicineImmunology and AllergyJHEP Reports
researchProduct

Regularity and h-polynomials of toric ideals of graphs

2020

For all integers 4 ≤ r ≤ d 4 \leq r \leq d , we show that there exists a finite simple graph G = G r , d G= G_{r,d} with toric ideal I G ⊂ R I_G \subset R such that R / I G R/I_G has (Castelnuovo–Mumford) regularity r r and h h -polynomial of degree d d . To achieve this goal, we identify a family of graphs such that the graded Betti numbers of the associated toric ideal agree with its initial ideal, and, furthermore, that this initial ideal has linear quotients. As a corollary, we can recover a result of Hibi, Higashitani, Kimura, and O’Keefe that compares the depth and dimension of toric ideals of graphs.

Hilbert seriesBetti numberGeneral MathematicsDimension (graph theory)0102 computer and information sciencesCommutative Algebra (math.AC)01 natural sciencesRegularityCombinatoricssymbols.namesakeMathematics - Algebraic GeometryCorollaryMathematics::Algebraic GeometryGraded Betti numbers; Graphs; Hilbert series; Regularity; Toric idealsFOS: MathematicsIdeal (ring theory)13D02 13P10 13D40 14M25 05E400101 mathematicsAlgebraic Geometry (math.AG)QuotientHilbert–Poincaré seriesMathematicsSimple graphDegree (graph theory)Mathematics::Commutative AlgebraApplied Mathematics010102 general mathematicsMathematics - Commutative AlgebraSettore MAT/02 - AlgebraToric ideals010201 computation theory & mathematicsGraded Betti numbers Graphs Hilbert series Regularity Toric idealssymbolsSettore MAT/03 - GeometriaGraded Betti numbersGraphs
researchProduct

Soluble E-Selectin Enhances Intercellular Adhesion Molecule-1 (ICAM-1) Expression in Human Tumor Cell Lines

1998

E-selectin mediates neovascularization via its soluble form, while its membrane-bound form initiates binding of tumor cells to vascular endothelium. Therefore, it was studied whether soluble E-selectin regulates further adhesion molecules on tumor cells. In tumor cells but not in related nonmalignant cells, intercellular adhesion molecule (ICAM)-1 expression was strikingly increased from 5 to 68% positive cells by in vitro inoculation of a recombinant E-selectin-IgG1 within 24 h, as analyzed by flow cytometry. The absence of changes in the expression of vascular cell adhesion molecule, integrin ligands (CD11a, CD18, integrin alpha 4), and sialyl-Lewis X indicates a specific effect of solubl…

ICAM3Time FactorsICAM2Cell adhesion moleculeT-LymphocytesIntercellular Adhesion Molecule-1Soluble cell adhesion moleculesGene ExpressionCell BiologyBiologyIntercellular Adhesion Molecule-1Intercellular adhesion moleculeMolecular biologyUp-RegulationCell biologySolubilityCell AdhesionTumor Cells CulturedHumansNeoplasm InvasivenessNeural cell adhesion moleculeRNA MessengerE-SelectinCell adhesionExperimental Cell Research
researchProduct