Search results for " carni"

showing 10 items of 21 documents

Brown bear behaviour in human-modified landscapes: The case of the endangered Cantabrian population, NW Spain

2018

Large carnivores are recolonizing parts of their historical range in Europe, a heavily modified human landscape. This calls for an improvement of our knowledge on how large carnivores manage to coexist with humans, and on the effects that human activity has on large carnivore behaviour, especially in areas where carnivore populations are still endangered. Brown bears Ursus arctos have been shown to be sensitive to the presence of people and their activities. Thus, bear conservation and management should take into account potential behavioural alterations related to living in human-modified landscapes. We studied the behaviour of brown bears in the Cantabrian Mountains, NW Spain, where an en…

0106 biological sciencesCantabrian mountainsRange (biology)PopulationEndangered speciesVigilance010603 evolutionary biology01 natural sciencesStress levelLarge carnivoreslcsh:QH540-549.5General patternCarnivoreUrsuseducationEcology Evolution Behavior and SystematicsNature and Landscape Conservationeducation.field_of_studyEcologybiologyEcologybiology.organism_classification010601 ecologyVideo recordingVigilance (behavioural ecology)GeographyHuman-dominated landscapesBrown bearlcsh:Ecology
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Record of a 10-year old European Wildcat Felis silvestris silvestris Schreber, 1777 (Mammalia: Carnivora: Felidae) from Mt. Etna, Sicily, Italy

2020

Longevity data for wild felids are lacking in the literature.  Here we report a camera trap recapture of a European Wildcat Felis silvestris at Mt. Etna in Sicily, Italy after nine years.  This individual was clearly identifiable as its tail ended with a white ring rather than the typical black ring and had a unique shape of the dorsal stripe.  At first capture on 26 May 2009, this cat was assessed as an adult, so that the likely minimum age of this individual at the time of recapture on 10 June 2018 must have been be at least 10 years.  This finding represents the oldest known European Wildcat in the wild and provides insight into age structure in wildcat populations.

0106 biological scienceslcsh:QH1-199.5biology.animal_breedcapture-recaptureZoologyManagement Monitoring Policy and Lawlcsh:General. Including nature conservation geographical distribution010603 evolutionary biology01 natural sciencesFelis silvestris silvestrilongevitysmall carnivoreslcsh:QH540-549.5CarnivoraSicilyEcology Evolution Behavior and SystematicsNature and Landscape Conservationbiologysmall wild cats010604 marine biology & hydrobiologyFelisEuropean Wildcatbiology.organism_classificationcamera trappingGeographyEuropean wildcatAnimal Science and Zoologylcsh:EcologyJournal of Threatened Taxa
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Invasive Species as Hosts of Zoonotic Infections: The Case of American Mink (Neovison vison) and Leishmania infantum

2021

Leishmania infantum produces an endemic disease in the Mediterranean Basin that affects humans and domestic and wild mammals, which can act as reservoir or minor host. In this study, we analyzed the presence of the parasite in wild American minks, an invasive species in Spain. We screened for L. infantum DNA by PCR using five primer pairs: Two targeting kinetoplast DNA (kDNA), and the rest targeting the ITS1 region, the small subunit of ribosomal RNA (SSU) and a repetitive sequence (Repeat region). The detection limit was determined for each method using a strain of L. infantum and a bone marrow sample from an infected dog. PCR approaches employing the Repeat region and kDNA (RV1/RV2 primer…

0301 basic medicineMicrobiology (medical)Sanidad animalQH301-705.5030231 tropical medicineRepeat regionMicrobiologyArticleNeovisonwild carnivore03 medical and health sciencesone health0302 clinical medicineVirologyparasitic diseasesmedicineParasite hostingAmerican minkBiology (General)leishmaniasisbiologySSUrRNAZoonosis030108 mycology & parasitologyRibosomal RNAzoonosisbiology.organism_classificationmedicine.diseaseVirologyAmerican minkKinetoplastkDNAInmunología veterinariahostsLeishmania infantumITSNested polymerase chain reactionMicroorganisms
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Late Carnian-Early Norian ammonoids from the GSSP candidate section Pizzo Mondello (Sicani mountain, Sicily).

2012

A small collection of ammonoids from the Upper Triassic Scillato Formation at Pizzo Mondello (Agrigento, Sicily) is studied. The specimens were collected in a framework of a project aimed at providing an integrated high-resolution bio-chronostratigraphic support to the Upper Carnian-Norian magnetostratigraphic scale defined at this site, that is located in an historical area from which G.G. Gemmellaro collected the Upper Triassic of ammonoids monographed at the beginning of the XX century. The specimens from Pizzo Mondello were bed-by-bed sampled and represent the first collection of Upper Triassic ammonoids described from Sicily since Gemmellaro time. Quite several levels of the Pizzo Mond…

Carnian/Norian boundarySicanian Domainlcsh:QE1-996.5AmmonoidsBiostratigraphyUpper Triassic; Carnian/Norian boundary; Ammonoids; Biostratigraphy; Sicily; Sicanian Domain; Scillato FormationScillato FormationSettore GEO/01 - Paleontologia E Paleoecologialcsh:GeologyUpper Triassic Norian GSSP Ammonoidea Pizzo Mondello Sicilylcsh:PaleontologyUpper TriassicSicilylcsh:QE701-760
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Zvaigžņotā Debess: 2012, Rudens (217)

2012

Saturs: P.Stučkas LVU ieguldījums astronomijas speciālistu sagatavošanā ; Starp "maldugunīm" un zvaigznēm ; A.Alksnis. Dawn kosmosa misija palīdz atklāt asteroīda Vesta noslēpumus ; D.Docenko. Komentārs: Par Higsa bozona atklāšanu ; I.P. Frīdriha Candera 125.dzimšanas dienai Krievijas Pasts izdevis marku ; P.Leckis. Mākoņu pārklātais pavadonis ; D.Kotlere, I.Šmelds. Kosmisko atlūzu novērojumi Ventspils Starptautiskajā radioastronomijas centrā ; Pirmo reizi “ZvD”: Dace Kotlere ; I.P. Divas dienas, godinot Jāni Ikaunieku (28.IV 1912.–27.IV 1969.) ; I.Pundure. Jāņa Ikaunieka devums Latvijas astronomijai ; N.Cimahoviča, Imants Vilks, R.Saveļjeva, T.Millers, A.Krastiņš. Atmiņas par Ikaunieku ; E…

Frīdriham Canderam – 125 (Pastmarkas)LVU astronomijas studenti – 1952. gada diplomandiSfērisks saules pulkstenis (Kocēni)Marss – nolaišanās bez izpletņiemKonkurss skolēniem OdysseusZvaigžņu tēma mākslā – dzeja un zīmējumiJānis IkaunieksLU Astronomiskā observatorija (vēsture):NATURAL SCIENCES::Physics::Astronomy and astrophysics [Research Subject Categories]Dawn misija – asteroīds VestaJauno zinātnieku EXPO 2012 Briselē – sarkano zvaigžņu pētījumiAstronomiskās parādības – 2012.gada rudenīFizikas docents Jānis Kariss (22.06.1927.-22.09.2011.)Higsa bozons – atklāšanaMagnusam Georgam Paukeram – 225Venēras pāriešana – novērojumi Rīgā Jūrmalā Carnikavā Ventspils novadāLatvijas 62. matemātikas olimpiāde – uzdevumiTitānsKosmiskās atlūzas – novērojumi Ventspils Starptautiskajā radioastronomijas centrā
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Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a severe fatty acid oxidation disorder

1994

3-Hydroxyacyl-CoA dehydrogenase deficiency is a newly recognised fatty acid oxidation disorder with a usually fatal outcome. We present a further patient who presented with hypoketotic hypoglycaemia, hepatopathy, secondary carnitine deficiency and increased plasma long-chain acylcarnitines. 3-Hydroxydicarboxylic aciduria was present and the diagnosis confirmed in cultured skin fibroblasts. Our patient is compared with those reported in the literature with respect to clinical symptoms, differential diagnosis and possible therapeutic regimens.

Malemedicine.medical_specialtyCardiomyopathyLipid Metabolism Inborn ErrorsFatal OutcomeInternal medicineCarnitineMedicineHumansBeta oxidationchemistry.chemical_classificationCultured skinbusiness.industryLiver DiseasesInfant Newborn3-Hydroxyacyl CoA DehydrogenasesMitochondrial MyopathiesClinical Enzyme Testsmedicine.diseaseDehydrogenase deficiencyHypoglycemiaEnzymeEndocrinologychemistrySecondary carnitine deficiencyPediatrics Perinatology and Child HealthDifferential diagnosisbusinessCardiomyopathiesLong-Chain-3-Hydroxyacyl-CoA DehydrogenaseEuropean journal of pediatrics
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Palazzo Abatellis, Matteo Carnilivari e i suoi collaboratori

2015

Il contributo esamina l'attività dell'architetto Matteo Carnelivari e quella dei suoi collaboratori nella Sicilia di fine Quattrocento. Sullo sfondo del cantiere di palazzo Abatellis e con l'ausilio della documentazione, la ricerca indaga la figura di Carnilivari, la sua formazione, le relazioni con la committenza e con i collaboratori locali e stranieri, i modelli desunti dall'architettura spagnola del XV secolo.

Matteo Carnilivari Committenti collaboratori architettura Sicilia XV secoloSettore ICAR/18 - Storia Dell'Architettura
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Tradizioni carnevalesche a Mezzojuso: dal Mastro di Campo al rogo del Nannu

2023

Il Mastro di Campo di Mezzojuso è una performance carnevalesca tradizionale che presenta un articolato simbolismo rituale riconducibile al pattern delle cerimonie di capodanno. In particolare si osservano il tema della ierogamia e della lotta rituale come elementi di promozione della fecondità. Ambedue i simboli rituali, la rappresentazione di una danza o di uno scontro armato, con l'eventuale coinvolgimento degli astanti e la celebrazione di un matrimonio, correlati o disgiunti, sono, come è noto, costitutivi ab antico delle cerimonie di capodanno, segnatamente di quelle primaverili. Altri rituali carnevaleschi europei hanno una simile articolazione. Il saggio presenta una serie di esempi …

Nozze sacre capodanno carnevale alberi metodo storico-comparativoSettore M-DEA/01 - Discipline DemoetnoantropologicheSacred marriage New Year Carnival trees historical-comparative method
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First Case Report of Primary Carnitine Deficiency Manifested as Intellectual Disability and Autism Spectrum Disorder

2019

Systemic primary carnitine deficiency (PCD) is a genetic disorder caused by decreased or absent organic cation transporter type 2 (OCTN2) carnitine transporter activity, resulting in low serum carnitine levels and decreased carnitine accumulation inside cells. In early life, PCD is usually diagnosed as a metabolic decompensation, presenting as hypoketotic hypoglycemia, Reye syndrome, or sudden infant death; in childhood, PCD presents with skeletal or cardiac myopathy. However, the clinical presentation of PCD characterized by autism spectrum disorder (ASD) with intellectual disability (ID) has seldom been reported in the literature. In this report, we describe the clinical features of a sev…

Pediatricsmedicine.medical_specialtymuscleautismrare diseaseCase ReportSLC22A5lcsh:RC321-57103 medical and health sciences0302 clinical medicineSystemic primary carnitine deficiencymedicineReye SyndromeCarnitineMyopathylcsh:Neurosciences. Biological psychiatry. Neuropsychiatry030304 developmental biology0303 health sciencesbiologybusiness.industryGeneral Neurosciencecarnitinemedicine.diseaseAutism spectrum disorderintellectual disabilitybiology.proteinAutismmedicine.symptombusinessPrimary Carnitine Deficiency030217 neurology & neurosurgerymedicine.drugBrain Sciences
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Mboat7 down-regulation by hyper-insulinemia induces fat accumulation in hepatocytes.

2020

Background: Naturally occurring variation in Membrane-bound O-acyltransferase domain-containing 7 (MBOAT7), encoding for an enzyme involved in phosphatidylinositol acyl-chain remodelling, has been associated with fatty liver and hepatic disorders. Here, we examined the relationship between hepatic Mboat7 down-regulation and fat accumulation. Methods: Hepatic MBOAT7 expression was surveyed in 119 obese individuals and in experimental models. MBOAT7 was acutely silenced by antisense oligonucleotides in C57Bl/6 mice, and by CRISPR/Cas9 in HepG2 hepatocytes. Findings: In obese individuals, hepatic MBOAT7 mRNA decreased from normal liver to steatohepatitis, independently of diabetes, inflammatio…

Research paperTGFβ Transforming Growth Factor BetaIntracellular SpaceCRISPR Clustered Regularly Interspaced Short Palindromic RepeatshHEPS Human HepatocytesMice0302 clinical medicineLPIAT1DAG Diacylglyceroli.p. Intraperitonealmedia_commonFatty AcidsGeneral Medicine3. Good health030220 oncology & carcinogenesisHOMA-IR homeostasis Model Assessment of Insulin ResistanceMPO morpholinolcsh:Medicine (General)medicine.medical_specialtyPE Phosphatidyl-EthanolamineNashGeneral Biochemistry Genetics and Molecular Biology03 medical and health sciencesTNFα tumor Necrosis Factor AlphaLDL Low Density LipoproteinsHyperinsulinismNAFLDSD Standard Dietmedia_common.cataloged_instanceHumansCPT1 Carnitine Palmitoyltransferase IPhosphatidylinositolGene SilencingEuropean unionVLDL Very Low Density Lipoproteinlcsh:RhHSC Human Hepatic Stellate Cellsmedicine.diseaseLipid MetabolismOA Oleic AcidCI Confidence IntervalMboat7 Membrane bound O-acyltransferase domain containing 7MCD methionine choline deficient diet030104 developmental biologyEndocrinologychemistryCDP Cytidine-DiphosphateFOXO1 Forkhead Box protein O1NAFLD nonalcoholic fatty liver diseaseSteatohepatitisBMI Body Mass IndexCL CardiolipinAcyltransferases0301 basic medicineAlcoholic liver diseaseCXCL10 C-X-C Motif Chemokine 10lcsh:Medicinechemistry.chemical_compoundNon-alcoholic Fatty Liver DiseaseIFG Impaired Fasting GlucoseAPOB Apolipoprotein BNonalcoholic fatty liver diseasePIP Phosphatidyl-Inositol-PhosphateSteatohepatitisqRT-PCR quantitative Real Time Polymerase Chain ReactionMice Knockoutlcsh:R5-920ORO Oil Red O StainingPI PhosphatidylinositolFatty liverTM6SF2 Transmembrane 6 Superfamily Member 2PhospholipidTAG TriglyceridesNASH Nonalcoholic SteatohepatitisLipogenesisLPA Lyso-Phosphatidic AcidPhosphatidylinositolSignal TransductionPS Phosphatidyl-SerinePA Palmitic AcidALD alcoholic liver diseasePC Phosphatidylcholinei.v. IntravenousFATP1 Fatty Acid Transport Protein 1Models BiologicalInternal medicinemedicineAnimalsNonalcoholic fatty liver diseasePPARα Peroxisome Proliferator-Activated Receptor alphaObesityG3P Glyceraldehyde-3-PhosphateSREBP1c Sterol Regulatory Element-Binding Protein 1HDL High Density Lipoproteinsbusiness.industryPI3K Phosphatidylinositol 3 KinaseMembrane ProteinsNHEJ Non-Homologues End JoiningPNPLA3 Patatin-like Phospholipase Domain-containing-3MTTP Microsomal Triglyceride Transfer ProteinLPIAT1 Lysophosphatidylinositol Acyltransferase 1TMC4 Transmembrane Channel-Like 4Disease Models AnimalGene Expression RegulationHepatocytesFOXA2 Forkhead Box A2mTOR mammalian target of RapamycinSteatosisInsulin ResistancebusinessPG Phosphatidyl-GlycerolFABP1 Fatty Acid-Binding Protein 1 FAS Fatty Acid SynthaseT2DM Type 2 Diabetes MellitusEBioMedicine
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