Search results for "Ilio"

showing 10 items of 429 documents

An Enigmatic European Harvestman (Opiliones): New Record and Redescription of Dicranopalpus larvatus (Canestrini, 1874)

2019

Dicranopalpus larvatus is redescribed based on type material. Recent first findings of this rare species on Sardinia enable to provide the essential morphological characters. Original drawings are presented with emphasis on penial and pedipalpal morphology. Dicranopalpus larvatus is a small, short-legged, ground-dwelling species endemic to Italy that matures in autumn and winter and has completed its life cycle in April. Additional information on phenology, life cycle, ecology, distribution and systematic position is given.

0106 biological sciencesSystematicsbiologyPhenologyRare species010607 zoologyZoologyMorphology (biology)Opilionesbiology.organism_classification010603 evolutionary biology01 natural sciencesGeographyType (biology)Insect ScienceDicranopalpusEcology Evolution Behavior and SystematicsArachnology
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A harvestman with elaborate palpal pliers, Thunbergia gretae n. gen. n. sp. from China (Opiliones: Sclerosomatidae: Gagrellinae)

2020

Abstract Based on the unusual characteristics of the male pedipalp and male genital morphology, a new genus and new species of Gagrellinae harvestmen, Thunbergia gretae n. gen. n. sp. (male and female) from Shaanxi Province, China, is proposed. The tibia and tarsus of the pedipalp form elaborate palpal claws, resembling gaspipe pliers, probably used to grasp the legs or the pedipalps of the female during courtship. There is no comparable modification of the pedipalp in the female. The penis lacks wing or sac-like (saccate) elements normally present in Gagrellinae, and the penis base is markedly inflated to form a bulb-like structure harbouring the penis muscle. Two or three opisthosomal ter…

0106 biological sciencesbiologyCourtship display010607 zoologySclerosomatidaeOpilionesAnatomybiology.organism_classification010603 evolutionary biology01 natural sciencesType speciesmedicine.anatomical_structureGenusmedicineAnimal Science and ZoologyPedipalpThunbergiaPenisZoologischer Anzeiger
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Social flexibility and social evolution in mammals: a case study of the African striped mouse (Rhabdomys pumilio)

2011

Environmental change poses challenges to many organisms. The resilience of a species to such change depends on its ability to respond adaptively. Social flexibility is such an adaptive response, whereby individuals of both sexes change their reproductive tactics facultatively in response to fluctuating environmental conditions, leading to changes in the social system. Social flexibility focuses on individual flexibility, and provides a unique opportunity to study both the ultimate and proximate causes of sociality by comparing between solitary and group-living individuals of the same population: why do animals form groups and how is group-living regulated by the environment and the neuro-en…

0106 biological scienceseducation.field_of_studybiologyEcology05 social sciencesPopulationbiology.organism_classification010603 evolutionary biology01 natural sciencesMate choiceSocial systemGeneticsBiological dispersal0501 psychology and cognitive sciences050102 behavioral science & comparative psychologySocial evolutioneducationPaternal careEcology Evolution Behavior and SystematicsSocialityRhabdomys pumilioMolecular Ecology
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Bachelor groups form due to individual choices or environmental disrupters in African striped mice

2021

International audience; In several mammal species, bachelor groups occur as a regular life history stage between dispersal and becoming the breeding male of a multi-female group. However, it is rarely investigated how such groups come into existence and how males that choose this strategy differ in life history traits from other males. Males of the socially flexible African striped mouse Rhabdomys pumilio have been historically reported to adopt one of three alternative tactics, i.e., small group-living philopatric males, intermediate solitary living roaming males, or large group-living territorial males. Here, we describe for the first time, bachelors as a fourth male tactic. Using long-te…

0106 biological sciencesmedia_common.quotation_subjecteducationBachelor010603 evolutionary biology01 natural sciencessocial flexibilityPredationLife history theorymale-male groups03 medical and health sciences[SDV.BA.ZV]Life Sciences [q-bio]/Animal biology/Vertebrate ZoologySeasonal breederLife historyEcology Evolution Behavior and Systematics030304 developmental biologymedia_common135-143 alternative reproductive tactics0303 health sciencesthermoregulationbiology182biology.organism_classificationreproductive successBiological dispersalAnimal Science and ZoologyPhilopatryAnimal Behaviouralternative reproductive tacticsstrategyRhabdomys pumilioDemography
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Evaluation of Planar-Cell-Polarity Phenotypes in Ciliopathy Mouse Mutant Cochlea

2016

In recent years, primary cilia have emerged as key regulators in development and disease by influencing numerous signaling pathways. One of the earliest signaling pathways shown to be associated with ciliary function was the non-canonical Wnt signaling pathway, also referred to as planar cell polarity (PCP) signaling. One of the best places in which to study the effects of planar cell polarity (PCP) signaling during vertebrate development is the mammalian cochlea. PCP signaling disruption in the mouse cochlea disrupts cochlear outgrowth, cellular patterning and hair cell orientation, all of which are affected by cilia dysfunction. The goal of this protocol is to describe the analysis of PCP…

0301 basic medicineCell signalingGeneral Chemical EngineeringStereocilia (inner ear)Cochlear ductBiologyGeneral Biochemistry Genetics and Molecular BiologyStereociliaMice03 medical and health sciencesHair Cells AuditorymedicineAnimalsCochleaGeneral Immunology and MicrobiologyGeneral NeuroscienceCiliumWnt signaling pathwayCell PolarityCochlear DuctEmbryo Mammalianmedicine.diseaseImmunohistochemistryCiliopathiesCochleaCell biologyDisease Models AnimalCiliopathyPhenotype030104 developmental biologymedicine.anatomical_structureMicroscopy Electron ScanningMedicinesense organsHair cellSignal TransductionJournal of Visualized Experiments
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OFIP/KIAA0753 forms a complex with OFD1 and FOR20 at pericentriolar satellites and centrosomes and is mutated in one individual with oral-facial-digi…

2016

Item does not contain fulltext Oral-facial-digital (OFD) syndromes are rare heterogeneous disorders characterized by the association of abnormalities of the face, the oral cavity and the extremities, some due to mutations in proteins of the transition zone of the primary cilia or the closely associated distal end of centrioles. These two structures are essential for the formation of functional cilia, and for signaling events during development. We report here causal compound heterozygous mutations of KIAA0753/OFIP in a patient with an OFD VI syndrome. We show that the KIAA0753/OFIP protein, whose sequence is conserved in ciliated species, associates with centrosome/centriole and pericentrio…

0301 basic medicineCentriolecell-cycle progressionGene Expressionmedicine.disease_causeCiliopathieshuman-disease genemolecular characterizationbbs proteinsGenetics (clinical)Conserved SequenceCentriolesGeneticsMutationCiliumCiliary transition zoneMetabolic Disorders Radboud Institute for Molecular Life Sciences [Radboudumc 6]General MedicineOrofaciodigital Syndromes3. Good healthcentriolar satellitesmultiple sequence alignmentbasal body dockingFemaleMicrotubule-Associated ProteinsProtein BindingHeterozygoteMolecular Sequence DataBiology03 medical and health sciencesIntraflagellar transportCiliogenesis[ SDV.MHEP ] Life Sciences [q-bio]/Human health and pathologyGeneticsmedicineHumansAmino Acid SequenceCiliaMolecular BiologyCentrosomeintraflagellar transportBase SequenceInfant NewbornProteins030104 developmental biologyCentrosomeMutationciliary transition zoneSequence Alignment[SDV.MHEP]Life Sciences [q-bio]/Human health and pathologyciliogenesis
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Universidad e Hispanidad. Tres décadas de trayectorias entrecruzadas del ministro José Ibáñez Martín y el catedrático exiliado Mariano Ruiz-Funes

2017

Presentamos la lucha desde el exilio intelectual republicano contra dos de las políticas del franquismo, la reforma de la universidad y la apropiación del término de hispanidad para los fines propagandísticos y proselitistas del nuevo régimen. Estas cuestiones son tratadas a partir de las trayectorias profesionales y vitales de dos políticos destacados, Mariano Ruiz-Funes y José Ibáñez Martín, desde sus inicios en la provincia de Murcia durante la década de 1920, en la cátedra de derecho penal uno y de enseñanza secundaria el otro, su militancia política, los servicios en misiones internacionales durante la guerra y, finalmente, la actividad de uno en la Unión de Profesores Universitarios E…

0301 basic medicineCultural StudiesHistorySecondary educationuniversidad españolaSociology and Political Scienceministros franquistasUniversitatsNational education03 medical and health sciencesAppropriationPolitics0302 clinical medicineexilio universitarioSociologyhispanidadLatin America. Spanish Americaexilio republicano españolF1201-3799lucha contra el franquismo030104 developmental biologySpanish Civil WarCriminal lawPolitical activismChristian ministryHumanities030217 neurology & neurosurgery
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Non-essential role for cilia in coordinating precise alignment of lens fibres

2016

The primary cilium, a microtubule-based organelle found in most cells, is a centre for mechano-sensing fluid movement and cellular signalling, notably through the Hedgehog pathway. We recently found that each lens fibre cell has an apically situated primary cilium that is polarised to the side of the cell facing the anterior pole of the lens. The direction of polarity is similar in neighbouring cells so that in the global view, lens fibres exhibit planar cell polarity (PCP) along the equatorial-anterior polar axis. Ciliogenesis has been associated with the establishment of PCP, although the exact relationship between PCP and the role of cilia is still controversial. To test the hypothesis t…

0301 basic medicineEmbryologyBBSomeBiologyArticle03 medical and health sciences0302 clinical medicineIntraflagellar transportMicrotubuleCiliogenesisLens CrystallineAnimalsBasal bodyLens placodeCiliaCells CulturedMice KnockoutTumor Suppressor ProteinsCiliumCell PolarityEpithelial CellsAnatomyCell biologyCytoskeletal Proteins030104 developmental biologyFiber cellMicrotubule-Associated Proteins030217 neurology & neurosurgeryDevelopmental BiologyMechanisms of Development
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p73 is required for ependymal cell maturation and neurogenic SVZ cytoarchitecture

2015

The adult subventricular zone (SVZ) is a highly organized microenvironment established during the first postnatal days when radial glia cells begin to transform into type B-cells and ependymal cells, all of which will form regenerative units, pinwheels, along the lateral wall of the lateral ventricle. Here, we identify p73, a p53 homologue, as a critical factor controlling both cell-type specification and structural organization of the developing mouse SVZ. We describe that p73 deficiency halts the transition of the radial glia into ependymal cells, leading to the emergence of immature cells with abnormal identities in the ventricle and resulting in loss of the ventricular integrity. p73-de…

0301 basic medicineEpendymal CellCiliumNeurogenesisSubventricular zoneBiology03 medical and health sciencesCellular and Molecular NeuroscienceLateral ventricles030104 developmental biologymedicine.anatomical_structureDevelopmental NeuroscienceCytoarchitectureCiliogenesismedicineskin and connective tissue diseasesEpendymaneoplasmsNeuroscienceDevelopmental Neurobiology
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Update on oral-facial-digital syndromes (OFDS)

2016

Oral-facial-digital syndromes (OFDS) represent a heterogeneous group of rare developmental disorders affecting the mouth, the face and the digits. Additional signs may involve brain, kidneys and other organs thus better defining the different clinical subtypes. With the exception of OFD types I and VIII, which are X-linked, the majority of OFDS is transmitted as an autosomal recessive syndrome. A number of genes have already found to be mutated in OFDS and most of the encoded proteins are predicted or proven to be involved in primary cilia/basal body function. Preliminary data indicate a physical interaction among some of those proteins and future studies will clarify whether all OFDS prote…

0301 basic medicineGeneticsCiliumOral facial digitalDevelopmental disorderDevelopmental disordersCell BiologyReviewBiologyBioinformaticsmedicine.diseasePhenotypeCiliopathiesHuman geneticsJoubert syndrome3. Good health03 medical and health sciences030104 developmental biologymedicineOFDSCiliaMeckel syndromeGene[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology
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