Search results for "ABC"

showing 10 items of 170 documents

Identification of novel mutations in the ABCA12 gene, c.1857delA and c.5653–5655delTAT, causing harlequin ichthyosis

2013

Abstract Harlequin ichthyosis (HI) is a severe autosomal recessive developmental disorder of the skin that is frequently but not always fatal in the first few days of life. In HI, mutations in both ABCA12 gene alleles must have a severe impact on protein function and most mutations are truncating. The presence of at least one nontruncating mutation (predicting a residual protein function) usually causes a less severe congenital ichthyosis (lamellar ichthyosis or congenital ichthyosiform erythroderma). Here we report on a girl with severe HI diagnosed by prenatal ultrasound at 33 5/7 week gestation. Ultrasound findings included ectropion, eclabium, deformed nose, hands and feet, joint contra…

Pathologymedicine.medical_specialtyCongenital ichthyosiform erythrodermaDNA Mutational AnalysisBiologyModels BiologicalPolymorphism Single NucleotideUltrasonography PrenatalExonFatal OutcomePregnancyCongenital ichthyosisGeneticsmedicineHumansABCA12Sequence DeletionGeneticsInfant NewbornEctropionGeneral MedicineLamellar ichthyosisHarlequin Ichthyosismedicine.diseaseEclabiumbiology.proteinATP-Binding Cassette TransportersFemalemedicine.symptomIchthyosis LamellarGene
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Visuomotor competencies and primary monosymptomatic nocturnal enuresis in prepubertal aged children

2013

Maria Esposito,1 Beatrice Gallai,2 Lucia Parisi,3 Michele Roccella,3 Rosa Marotta,4 Serena Marianna Lavano,4 Giovanni Mazzotta,5 Giuseppina Patriciello,1 Francesco Precenzano,1 Marco Carotenuto1 1Clinic of Child and Adolescent Neuropsychiatry, Department of Mental Health, Physical and Preventive Medicine, Second University of Naples, Italy; 2Unit of Child and Adolescent Neuropsychiatry, University of Perugia, Italy; 3Child Neuropsychiatry, Department of Psychology, University of Palermo, Italy; 4Department of Psychiatry, "Magna Graecia" University of Catanzaro, Catanzaro, Italy; 5Unit of Child and Adolescent Neuropsychiatry, AUSL Umbria 2, Terni, Italy Background: Primary …

Pediatricsmedicine.medical_specialtyNeuropsychiatric Disease and TreatmentPopulationNeurosciences. Biological psychiatry. Neuropsychiatryprimary monosymptomatic nocturnal enuresis visuomotor integration childhood rehabilitation VMI M-ABCEnuresisvisuomotor integrationmedicineMass indexM-ABCRC346-429educationBiological PsychiatryOriginal Researcheducation.field_of_studyIntelligence quotientbusiness.industrychildhood rehabilitationprimary monosymptomatic nocturnal enuresisVMISettore MED/39 - Neuropsichiatria InfantileMotor coordinationPsychiatry and Mental healthLanguage developmentLearning disabilityPopulation studyNeurology. Diseases of the nervous systemmedicine.symptombusinessRC321-571
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Ecos de la Junta democrática y de la oposición en el diario ABC (1974-75): la ruptura como pesadilla

2012

International audience; La creación de la Junta democrática como plataforma antifranquista se proponía romper con las instituciones del Régimen iniciando una lucha pacífica que debía permitir una democratización radical del estado. La ruptura con las instituciones del franquismo debía ser llevada a cabo gracias a un gobierno provisional representativo de todas las fuerzas de oposición. Las numerosas acciones y comunicaciones a los órganos de prensa internacionales de la Comisión Exterior de la Junta democrática de España, dirigida por José Vidal Beneyto, permitieron a la JDE darse a conocer a los países europeos siendo aún ilegal dentro del país. Los artículos del diario ABC de 1974-75 se h…

PesadillaOpus Dei[SHS.LITT]Humanities and Social Sciences/LiteraturePlataforma antifranquistaEspañaAnticomunismo estadounidenseIzquierdaAmenazasPSOEPartido Socialista PopularMiedoAntifranquismoComisión ExterioranticomunismoOposiciónDemocraciaPoderCalumnias030504 nursing06 humanities and the artsGeneral Medicinelcsh:PN1-6790Acción políticaTribunalcsh:PQ1-39990602 languages and literatureLuchaRaúl Morodo0305 other medical scienceABCVidal-Beneyto Josélcsh:Literature (General)PolíticaOposición ilegalTierno Galván03 medical and health sciencesrepresiónGarcía TrevijanoPatriaCaosDionisio RidruejoDictadurafranquismoSobre José Vidal-Beneyto: Reseñas críticas y referencias a la obra de Vidal-Beneyto060201 languages & linguisticslcsh:French literature - Italian literature - Spanish literature - Portuguese literatureCensuraTransiciónRupturaComunismoPrensaJOSÉ VIDAL-BENEYTOMonarquíaprensa española (siglo XX)Partido ComunistaAcciones: Acciones de una vida: Democracia (I)Junta democráticaBabel
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2015

Multidrug resistance is a prevailing phenomenon leading to chemotherapy treatment failure in cancer patients. In the current study two known cytotoxic pseudoguaianolide sesquiterpene lactones; neoambrosin (1) and damsin (2) that circumvent MDR were identified. The two cytotoxic compounds were isolated using column chromatography, characterized using 1D and 2D NMR, MS, and compared with literature values. The isolated compounds were investigated for their cytotoxic potential using resazurin assays and thereafter confirmed with immunoblotting and in silico studies. MDR cells overexpressing ABC transporters (P-glycoprotein, BCRP, ABCB5) did not confer cross-resistance toward (1) and (2), indic…

PharmacologyMultiple drug resistanceCancer cellCytotoxic T cellABCB5Pharmacology (medical)ATP-binding cassette transporterTransfectionKinase activityPharmacologyBiologyCytotoxicityMolecular biologyFrontiers in Pharmacology
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Defense Responses of Fusarium oxysporum to 2,4-Diacetylphloroglucinol, a Broad-Spectrum Antibiotic Produced by Pseudomonas fluorescens

2004

A collection of 76 plant-pathogenic and 41 saprophytic Fusarium oxysporum strains was screened for sensitivity to 2,4-diacetylphloroglucinol (2,4-DAPG), a broad-spectrum antibiotic produced by multiple strains of antagonistic Pseudomonas fluorescens. Approximately 17% of the F. oxysporum strains were relatively tolerant to high 2,4-DAPG concentrations. Tolerance to 2,4-DAPG did not correlate with the geographic origin of the strains, formae speciales, intergenic spacer (IGS) group, or fusaric acid production levels. Biochemical analysis showed that 18 of 20 tolerant F. oxysporum strains were capable of metabolizing 2,4-DAPG. For two tolerant strains, analysis by mass spectrometry indicated…

PhysiologyPhloroglucinolPseudomonas fluorescensPhloroglucinoltomatoPseudomonas fluorescensMicrobiologyresistancestrainschemistry.chemical_compoundFusariumtake-allDrug Resistance BacterialFusarium oxysporum[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular Biology[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologybiocontrolPhylogenyPlant DiseasesDose-Response Relationship DrugbiologyEPS-2food and beveragesgenetic diversityGeneral MedicineFungi imperfectiPlantspopulationssensitivitybiology.organism_classificationAnti-Bacterial AgentsLaboratorium voor PhytopathologiePRI BiosciencechemistryLaboratory of PhytopathologyPseudomonadales24-DiacetylphloroglucinolDNA Intergenicbiosynthesisabc transportersAgronomy and Crop ScienceFusaric acidPseudomonadaceaeMolecular Plant-Microbe Interactions®
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Templated synthesis of a large and flexible covalent porphyrinic cage bearing orthogonal recognition sites.

2012

A large covalent cage incorporating two porphyrins attached by four long and flexible polyether chains each bearing two 3-pyridyl ligands was synthesized from a DABCO-templated olefin metathesis reaction. The X-ray structure of the cage with the DABCO coordinated inside the cavity to the two zinc(II) porphyrins reveals a highly symmetric structure.

PorphyrinsSymmetric structureStereochemistryMolecular Conformationchemistry.chemical_elementZincDABCOCrystallography X-RayLigandsCatalysisMolecular conformationPiperazineslaw.inventionchemistry.chemical_compoundlawPolymer chemistryMaterials Chemistryta116Bearing (mechanical)Olefin metathesisMetals and AlloysGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsZincchemistryCovalent bondCeramics and CompositesCageChemical communications (Cambridge, England)
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Pharmacological Induction of Redundant Genes for a Therapy of X-ALD

2003

X-linked adrenoleukodystrophy (X-ALD) is a recessive neurologic disease with an incidence among males of 1/17 000. Since the identification of the X-ALD gene (ABCD1) ten years ago (Mosser et al 1993), no satisfactory therapy has been available. A close homologue (ABCD2) was then cloned and presented as a putative modifier gene that could account for some of the extreme phenotypic variability of X-ALD (Lombard-Platet et al 1996). The inducibility of Abcd2 by the hypolipidemic drug fenofibrate in the liver of rodents (Albet et al 1997), correlated to a partial normalisation of the biochemical phenotype of X-ALD (Netik et al 1999), opened up the way of a pharmacological therapy of X-ALD. The b…

Pristanic acidcongenital hereditary and neonatal diseases and abnormalitiesFenofibrateendocrine system diseasesPharmacological therapybiologyPharmacologymedicine.diseasePhenylbutyrateBiochemical phenotypechemistry.chemical_compoundchemistrymedicineABCD2biology.proteinAdrenoleukodystrophyGenemedicine.drug
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2014

In a subset of inherited retinal degenerations (including cone, cone-rod, and macular dystrophies), cone photoreceptors are more severely affected than rods; ABCA4 mutations are the most common cause of this heterogeneous class of disorders. To identify retinal-disease-associated genes, we performed exome sequencing in 28 individuals with “cone-first” retinal disease and clinical features atypical for ABCA4 retinopathy. We then conducted a gene-based case-control association study with an internal exome data set as the control group. TTLL5, encoding a tubulin glutamylase, was highlighted as the most likely disease-associated gene; 2 of 28 affected subjects harbored presumed loss-of-function…

ProbandGeneticsbiologyABCA4RetinalMolecular biology3. Good healthchemistry.chemical_compoundchemistryGeneticsbiology.proteinMissense mutationsense organsExomePolyglutamylationGenetics (clinical)Retinal DystrophiesExome sequencingThe American Journal of Human Genetics
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Silymarin and Cancer: A Dual Strategy in Both in Chemoprevention and Chemosensitivity

2020

Silymarin extracted from milk thistle consisting of flavonolignan silybin has shown chemopreventive and chemosensitizing activity against various cancers. The present review summarizes the current knowledge on the potential targets of silymarin against various cancers. Silymarin may play on the system of xenobiotics, metabolizing enzymes (phase I and phase II) to protect normal cells against various toxic molecules or to protect against deleterious effects of chemotherapeutic agents on normal cells. Furthermore, silymarin and its main bioactive compounds inhibit organic anion transporters (OAT) and ATP-binding cassettes (ABC) transporters, thus contributing to counteracting potential chemor…

Programmed cell deathsilymarinCellChemosensitizerPharmaceutical SciencechemopreventiveATP-binding cassette transporterApoptosisReviewProtective AgentsChemopreventionsilybinAnalytical Chemistrylcsh:QD241-44103 medical and health sciences0302 clinical medicinelcsh:Organic chemistryDrug DiscoverymedicineHumansPhysical and Theoretical ChemistryReceptor030304 developmental biology0303 health sciencesChemistryOrganic ChemistryCancerCell Cycle CheckpointsCell cyclemedicine.diseasemedicine.anatomical_structureChemistry (miscellaneous)intrinsic and extrinsic pathwayDrug Resistance Neoplasm030220 oncology & carcinogenesisCancer cellchemosensitizerCancer researchMolecular Medicinemetabolizing enzymesATP-Binding Cassette Transporterscell cycleABC transporterSignal TransductionMolecules
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6-mercaptopurine and 9-(2-phosphonyl-methoxyethyl) adenine (PMEA) transport altered by two missense mutations in the drug transporter gene ABCC4

2008

Multiple drug resistance protein 4 (MRP4, ABCC4) belongs to the C subfamily of the ATP-binding cassette (ABC) transporter superfamily and participates in the transport of diverse antiviral and chemotherapeutic agents such as 6-mercaptopurine (6-MP) and 9-(2-phosphonyl methoxyethyl) adenine (PMEA). We have undertaken a comprehensive functional characterization of protein variants of MRP4 found in Caucasians and other ethnicities. A total of 11 MRP4 missense genetic variants (nonsynonymous SNPs), fused to green fluorescent protein (GFP), were examined in Xenopus laevis oocytes for their effect on expression, localization, and function of the transporter. Radiolabeled 6-MP and PMEA were chosen…

Recombinant Fusion ProteinsGreen Fluorescent ProteinsMutation MissenseOrganophosphonatesXenopusATP-binding cassette transporterABCC4BiologyGreen fluorescent proteinXenopus laevisGeneticsAnimalsHumansMissense mutationGenetics (clinical)DNA Primerschemistry.chemical_classificationBase SequenceMercaptopurineAdenineWild typebiology.organism_classificationMolecular biologyTransmembrane proteinAmino acidchemistryBiochemistryMutagenesis Site-Directedbiology.proteinMultidrug Resistance-Associated ProteinsHuman Mutation
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