Search results for "Dwarf"

showing 10 items of 136 documents

LOW VIGOR PEACH × ALMOND ROOTSTOCKS FOR INTENSIVE PEACH PLANTINGS IN MEDITERRANEAN ENVIRONMENTS

2014

A three-year trial was carried out to evaluate the vegetative and productive performance of five peach rootstocks of varied vigor. The study was conducted in south-western Sicily using 45 V-trained trees of 'Tropic Snow' peach planted in 2005 and grafted on GF677 and four low-vigor rootstocks selected at the Department of Agricultural, Food and Environmental Sciences, University of Pisa, namely IS5/8 (Polluce), IS5/19 (Castore), IS5/23, IS5/29. Trunk circumference, winter and summer pruning weight, number and mass of fruit were recorded from 2010 to 2012. All IS selections reduced trunk cross-sectional area (TCSA) and pruning weight compared to GF677 with IS5/23 inducing the highest reducti…

crop load dwarfing fruit size Prunus persica tree vigor yieldSettore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreeMediterranean climateHorticultureAgronomyHorticultureBiologyRootstockActa Horticulturae
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Incantesimi in inglese antico contro un dweorg

2021

The word dweorg with the meaning ‘dwarf’ was certainly available in Anglo-Saxon England, as attested to by the earliest glossaries, such as those of Épinal and Erfurt, where it is used to render the Latin nanus and pumilio. OE dweorg also occurs in a group of five charms and medical recipes, where it seems to designate an ailment, characterized by a strong and sudden onset of fever. Particularly, in the remedies contained in the Medicina de quadrupedibus and in the Peri didaxeon – both translations of Latin medical treatises – OE dweorg means ‘fever’. In the Old English period, the semantic value of the term shifted, ending up to denote the pathological condition itself. More specifically, …

dwarf Old English charms Anglo-Saxon Medicine and MagicSettore L-FIL-LET/15 - Filologia Germanica
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Defining the Island Dwarfing Rate of an Extinct Sicilian Elephant Using Ancient DNA

2020

Evolution on islands, and the often extreme phenotypic changes associated with it, has attracted much interest from evolutionary biologists. However, measuring the rate of change of a particular phenotypic trait of extinct animals can be challenging, due to the incompleteness of the fossil record. Here, we use combined molecular and fossil evidence to define the minimum and maximum rate of dwarfing in an extinct Mediterranean dwarf elephant from Puntali Cave (Sicily). Despite the challenges associated with recovering ancient DNA from warm climates, we successfully retrieved a mitogenome from a sample with an estimated age between 147,000 and 50,000 years. Our results suggest that this speci…

geographygeography.geographical_feature_categoryPleistocenePalaeoloxodonbiologyLineage (evolution)Phenotypic traitbiology.organism_classificationlanguage.human_languageDwarfingAncient DNACaveEvolutionary biologylanguageSicilianSSRN Electronic Journal
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Progenitor death drives retinal dysplasia and neuronal degeneration in a mouse model of Atrip-Seckel syndrome

2020

ABSTRACT Seckel syndrome is a type of microcephalic primordial dwarfism (MPD) that is characterized by growth retardation and neurodevelopmental defects, including reports of retinopathy. Mutations in key mediators of the replication stress response, the mutually dependent partners ATR and ATRIP, are among the known causes of Seckel syndrome. However, it remains unclear how their deficiency disrupts the development and function of the central nervous system (CNS). Here, we investigated the cellular and molecular consequences of ATRIP deficiency in different cell populations of the developing murine neural retina. We discovered that conditional inactivation of Atrip in photoreceptor neurons …

lcsh:MedicineMedicine (miscellaneous)315BlindnessMicechemistry.chemical_compoundImmunology and Microbiology (miscellaneous)Cell DeathneurodevelopmentStem CellsNeurodegenerationapoptosisneurodegenerationSyndromeCell biologyDNA-Binding Proteinsdna damage responsemedicine.anatomical_structurePhotoreceptor Cells VertebrateResearch Articlelcsh:RB1-214NeurogenesisNeuroscience (miscellaneous)Embryonic DevelopmentBiologyRetinaGeneral Biochemistry Genetics and Molecular Biologylcsh:PathologymedicineAnimalsAbnormalities MultipleProgenitor cellVision OcularAdaptor Proteins Signal TransducingCell ProliferationProgenitorRetinalcsh:RRetinalEmbryo Mammalianmedicine.diseasephotoreceptorDisease Models AnimalSeckel syndromechemistryvisual system developmentNerve DegenerationRetinal dysplasiaRetinal DysplasiaTumor Suppressor Protein p53Primordial dwarfismDNA DamageDisease Models & Mechanisms
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The VST Photometric Hα Survey of the Southern Galactic Plane and Bulge (VPHAS+)

2014

The VST Photometric Halpha Survey of the Southern Galactic Plane and Bulge (VPHAS+) is surveying the southern Milky Way in u, g, r, i and Halpha at 1 arcsec angular resolution. Its footprint spans the Galactic latitude range -5 < b < +5 at all longitudes south of the celestial equator. Extensions around the Galactic Centre to Galactic latitudes +/-10 bring in much of the Galactic Bulge. This ESO public survey, begun on 28th December 2011, reaches down to 20th magnitude (10-sigma) and will provide single-epoch digital optical photometry for around 300 million stars. The observing strategy and data pipelining is described, and an appraisal of the segmented narrowband Halpha filter in us…

media_common.quotation_subjectMilky WayAstronomyFOS: Physical sciencesAstrophysicsAstrophysics::Cosmology and Extragalactic Astrophysics7. Clean energyPhotometry (optics)BulgeQB460Astrophysics::Solar and Stellar AstrophysicsQCAstrophysics::Galaxy Astrophysicsmedia_commonQBPhysicsCelestial equatorWhite dwarfAstronomyAstronomy and AstrophysicsGalactic planeAstrophysics - Astrophysics of GalaxiesStars13. Climate actionSpace and Planetary ScienceSkyAstrophysics of Galaxies (astro-ph.GA)ComputingMethodologies_DOCUMENTANDTEXTPROCESSINGAstrophysics::Earth and Planetary Astrophysics
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Autosomal recessive severe dwarfism in a Sicilian girl: a new form of osteodysplastic primordial dwarfism?

1996

A new type of osteodysplastic primordial dwarfism is delineated in a 5- year-old female child with severe growth retardation of prenatal onset, gross skeletal changes, a non-Seckel facial phenotype, and presumed autosomal recessive inheritance.

media_common.quotation_subjectgrowth retardationDwarfismDwarfismGenes RecessiveOsteodysplastic primordial dwarfismBiologyBone and BonesCraniofacial AbnormalitiesConsanguinitymedicineHumansAbnormalities MultipleGirlGenetics (clinical)media_commonGeneticsAutosomal recessive inheritanceGrowth retardationautosomal recessive inheritancemedicine.diseasePrenatal onsetOsteochondrodysplasiaRadiographyChild Preschoolosteodysplastic primordial dwarfismFemalesense organsAmerican journal of medical genetics
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The effect of nacom (L-dopa and L-carbidopa) on growth hormone secretion in 75 patients with short stature.

1977

The stimulatory effect of Nacom (250 mg L-Dopa and 25 mg L-Carbidopa) on the HGH secretion was evaluated in 75 short stature patients. The number of blood samples was restricted to only three (0, 45 and 90 min). 63 patients reached adequate HGH concentrations after the ingestion of 1 tablet Nacom (84%). Somatotropin levels increased from 2.08 (Sx 0.28) to a maximal HGH value of 14.22 (Sx 0.87) ng/ml. When the stimulatory effect of Nacom was compared with the standard method of arginine infusion in children with normal stature the arginine test was not superior to the Nacom-test. The Nacom-test appears to be a simple and reliable screening method for HGH deficiency, particularly in outpatien…

medicine.medical_specialtyAdolescentArginine testDwarfismArginineShort statureInternal medicineMedicineIngestionHumansChildbusiness.industryCarbidopaGrowth hormone secretionDihydroxyphenylalanineEndocrinologyHydrazinesCarbidopaChild PreschoolGrowth HormonePediatrics Perinatology and Child Healthmedicine.symptombusinessSecretory Ratehormones hormone substitutes and hormone antagonistsmedicine.drugEuropean journal of pediatrics
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LARP7 variants and further delineation of the Alazami syndrome phenotypic spectrum among primordial dwarfisms: 2 sisters.

2019

Abstract Alazami syndrome (AS) (MIM# 615071 ) is an autosomal recessive microcephalic primordial dwarfism (PD) with recognizable facial features and severe intellectual disability due to depletion or loss of function variants in LARP7. To date, 15 patients with AS have been reported. Here we describe two consanguineous Algerian sisters with Alazami PD due to LARP7 homozygous pathogenic variants detected by whole exome sequencing. By comparing these two additional cases with those previously reported, we strengthen the key features of AS: severe growth restriction, severe intellectual disability and some distinguishing facial features such as broad nose, malar hypoplasia, wide mouth, full li…

medicine.medical_specialtyHeart malformation[SDV]Life Sciences [q-bio]Dwarfism03 medical and health sciencesLoss of Function MutationIntellectual DisabilityIntellectual disabilityGeneticsmedicineHumansChildGenetics (clinical)Exome sequencingLoss function030304 developmental biology0303 health sciencesbusiness.industrySiblings030305 genetics & heredityGeneral MedicineSyndromemedicine.diseaseDermatologyPhenotype[SDV] Life Sciences [q-bio]PhenotypeRibonucleoproteinsEtiologyMicrocephalyFemalePrimordial dwarfismbusinessMild microcephalyEuropean journal of medical genetics
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A rare form of spondylometaphyseal dysplasia-type A4

1998

We present 2 cases of a previously apparently unreported spondylo-metaphyseal dysplasia comprising dwarfism, severe metaphyseal changes, ovoid vertebrae and mild platyspondyly with anterior tonguing of the vertebral bodies. The inheritance may be autosomal recessive.

musculoskeletal diseasesmedicine.medical_specialtybusiness.industryDwarfismOvoid vertebraeAnatomymusculoskeletal systemmedicine.diseaseOsteochondrodysplasiaEndocrinologySpondylometaphyseal dysplasiaDysplasiaInternal medicinemedicinePlatyspondylysense organsMild platyspondylyCongenital diseasebusinessGenetics (clinical)American Journal of Medical Genetics
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WRKY gene family drives dormancy release in onion bulbs

2022

Onion (Allium cepa L.) is an important bulb crop grown worldwide. Dormancy in bulbous plants is an important physiological state mainly regulated by a complex gene network that determines a stop of vegetative growth during unfavorable seasons. Limited knowledge on the molecular mechanisms that regulate dormancy in onion were available until now. Here, a comparison between uninfected and onion yellow dwarf virus (OYDV)-infected onion bulbs highlighted an altered dormancy in the virus-infected plants, causing several symptoms, such as leaf striping, growth reduction, early bulb sprouting and rooting, as well as a lower abscisic acid (ABA) level at the start of dormancy. Furthermore, by compar…

onion yellow dwarf virusPotyvirusfungiAllium cepa Lfood and beveragesSettore CHIM/06 - Chimica OrganicaGeneral Medicinede novo transcriptome assemblyOnion yellow dwarf virusGibberellinsPlant BreedingLaboratorium voor Plantenveredelingbiotic stressBiotic stressGene Expression Regulation PlantOnions<i>Allium cepa</i> L.; onion yellow dwarf virus; de novo transcriptome assembly; transcription factor; RNA-seq; biotic stressGene Regulatory NetworksTranscription factorRNA-seqDe novo transcriptome assemblytranscription factorAbscisic Acid
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