RESUMO
We report measurements of quantum oscillations detected in the putative nematic phase of Sr3Ru2O7. Improvements in sample purity enabled the resolution of small amplitude de Haas-van Alphen (dHvA) oscillations between two first order metamagnetic transitions delimiting the phase. Two distinct frequencies were observed, whose amplitudes follow the normal Lifshitz-Kosevich profile. Variations of the dHvA frequencies are explained in terms of a chemical potential shift produced by reaching a peak in the density of states, and an anomalous field dependence of the oscillatory amplitude provides information on domains.
RESUMO
We present a detailed quantum oscillation study of the Fermi surface of the recently discovered Yb-based heavy fermion superconductor beta-YbAlB4. We compare the data, obtained at fields from 10 to 45 T, to band structure calculations performed using the local density approximation. Analysis of the data suggests that f holes participate in the Fermi surface up to the highest magnetic fields studied. We comment on the significance of these findings for the unconventional superconducting properties of this material.
Assuntos
Sistema Límbico/metabolismo , Miocárdio/metabolismo , Canais de Sódio/genética , Animais , Autorradiografia/métodos , Hibridização In Situ , Canal de Sódio Disparado por Voltagem NAV1.5 , Neurônios/metabolismo , Sondas de Oligonucleotídeos , Especificidade de Órgãos , Células Piramidais/metabolismo , Ratos , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Canais de Sódio/análise , Radioisótopos de EnxofreRESUMO
The nervous system maintains a delicate balance between excitation and inhibition, partly through the complex interplay between voltage-gated sodium and potassium ion channels. Because K+ channel blockade or gene deletion causes hyperexcitability, it is generally assumed that increases in K+ channel gene expression should reduce neuronal network excitability. We have tested this hypothesis by creating a transgenic mouse that expresses a Shaker-type K+ channel gene. Paradoxically, we find that addition of the extra K+ channel gene results in a hyperexcitable rather than a hypoexcitable phenotype. The presence of the transgene leads to a complex deregulation of endogenous Shaker genes in the adult central nervous system as well as an increase in network excitability that includes spontaneous cortical spike and wave discharges and a lower threshold for epileptiform bursting in isolated hippocampal slices. These data suggest that an increase in K+ channel gene dosage leads to dysregulation of normal K+ channel gene expression, and it may underlie a mechanism contributing to the pathogenesis of human aneuploidies such as Down syndrome.
Assuntos
Encéfalo/fisiologia , Regulação da Expressão Gênica , Neurônios/fisiologia , Canais de Potássio/fisiologia , Animais , Córtex Cerebral/fisiologia , Giro Denteado/fisiologia , Eletroencefalografia , Hipocampo/fisiologia , Humanos , Hibridização In Situ , Camundongos , Camundongos Transgênicos , Fenótipo , Canais de Potássio/genética , RNA Mensageiro/análise , Proteínas Recombinantes/metabolismo , Superfamília Shaker de Canais de Potássio , Transcrição GênicaRESUMO
ABSTRACT The amount of defoliation of elm (Ulmus procera) caused by three Ophiostoma novoulmi Eurasian race isolates over 14 seasons of field trials was found to be strongly correlated with mean air temperature and mean number of sunshine hours over the 12-week period from inoculation to assessment, and with tree age. The coefficient of determination for the regression of percent defoliation on the environmental and tree factors was 0.76, P < 0.001 (33 df). Levels of defoliation were greatest when mean air temperatures exceeded 17 degrees C with moderate light (5 to 7 h of sunshine), and lowest under conditions of either high light (>7.5 h of sunshine) at all air temperatures or low light (<4.5 h of sunshine) and air temperatures of less than 15.5 degrees C. The model varied in its intercept for the three isolates, reflecting their different levels of aggressiveness. The role of environmental factors in the development of Dutch elm disease symptoms and the implications for elm resistance breeding are discussed.
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The transition to managed care raises concerns about the resulting quality of care. The report card, a publicly released, standardized report on quality, has received widespread acceptance as a method to evaluate physician performance. Current report cards provide insufficient information to allow purchasers of health care to assess accurately the performance of professionals who provide breast care. To overcome these limitations, we propose an expanded report card on breast cancer care. Mammographers and general surgeons would assess an independent series of at least 100 consecutive cases of newly diagnosed breast cancer. Mammographers would determine the percentage of invasive cancers < 15 mm detected on screening mammograms in asymptomatic women aged 50 to 74 years. Surgeons would determine the percentage of combined stages 0 and 1 breast cancers detected and the percentage of patients receiving breast-conserving surgical therapy. Performance targets are set at 60% for invasive cancers < 15 mm detected on screening mammography, 60% for combined stage 0 and 1 breast cancers, and 50% for patients receiving breast-conserving therapy.
Assuntos
Neoplasias da Mama/prevenção & controle , Programas de Assistência Gerenciada/normas , Programas de Rastreamento/normas , Avaliação de Processos e Resultados em Cuidados de Saúde , Qualidade da Assistência à Saúde/normas , Idoso , Neoplasias da Mama/diagnóstico por imagem , Neoplasias da Mama/patologia , Competência Clínica , Feminino , Reforma dos Serviços de Saúde/normas , Humanos , Mamografia , Pessoa de Meia-Idade , Estadiamento de Neoplasias , Estados UnidosRESUMO
Neuronal migration, differentiation, and synapse formation are developmental processes within the CNS significantly influenced by ionotropic and metabotropic glutamate receptor activity. Extracellular glutamate concentrations mediating this activity are regulated by transport proteins localized in neuronal and glial cell membranes. We have used in situ hybridization analysis with subtype-specific antisense-oligonucleotides to study the distribution of glia-specific excitatory amino acid transporter (mEAAT1 and mEAAT2) mRNAs during the later stages of embryogenesis and postnatal CNS development. Distinct but overlapping embryonic and postnatal patterns of localization were observed for the two transporter transcripts. Both mEAAT1 and mEAAT2 mRNAs were found during the peak period of gliogenesis (E15-E19) in the telencephalic and mesencephalic CNS proliferative zones. The overall expression of mEAAT1 mRNA diminished after the completion of cell migration, whereas mEAAT2 mRNA expression increased significantly during postnatal development. Interestingly, mEAAT2 transcript expression continued in the subventricular zone postnatally and persisted in this proliferative zone in the adult brain. From PO onward, mEAAT1 mRNA was present predominantly in the cerebellar Purkinje cell layer and at a much lower abundance in the cortex, hippocampus, basal nuclei, and septum, whereas from P7 onward, mEAAT2 mRNA expression increased throughout most of the neuraxis. Postnatally, transcripts for mEAAT1 and mEAAT2 were found in cell bodies, processes, and commissural white matter tracts of the CNS. The divergent temporal and spatial expression of EAAT subtypes and their persistence in mature fiber tracts and radial glia layers reveal that specific EAATs are likely to play multiple distinct roles in the developing and adult CNS, including the regulation of cell proliferation, axon-glia interactions, and neuronal survival.
Assuntos
Transportadores de Cassetes de Ligação de ATP/genética , Encéfalo/fisiologia , Fatores Etários , Sequência de Aminoácidos , Sistema X-AG de Transporte de Aminoácidos , Animais , Axônios/fisiologia , Gânglios da Base/fisiologia , Sequência de Bases , Transporte Biológico/fisiologia , Química Encefálica/fisiologia , Cerebelo/fisiologia , Córtex Cerebral/fisiologia , Diencéfalo/fisiologia , Embrião de Mamíferos/fisiologia , Regulação da Expressão Gênica no Desenvolvimento/fisiologia , Hipocampo/fisiologia , Hibridização In Situ , Camundongos , Camundongos Endogâmicos C57BL , Dados de Sequência Molecular , Neuroglia/fisiologia , Neuroglia/ultraestrutura , RNA Mensageiro/análise , Transcrição Gênica/fisiologiaRESUMO
Defined transgenic models of epilepsy in the mouse represent unique opportunities to examine interactions between synchronous synaptic activity and cellular programs of brain development. We are beginning to acquire a list of the kinds of genes favoring sudden, intermittent aberrant discharges in central neurons, and we have found that, rather than arising from a few gene superfamilies regulating membrane excitability, they are involved in many diverse functions of the cell. Whereas some primary gene defects impinge directly on membrane electrogenesis and neurotransmitter signaling at synapses, others are too far removed from these processes to clearly visualize the steps by which they promote epileptogenesis. We have tantalizing evidence that several, and probably all, epilepsy genes entrain some degree of secondary molecular and cellular plasticity, and we can guess that these downstream rearrangements may account for the delayed onset of epileptic phenotypes in some syndromes. It is too early to tell whether these, or other induced changes, provide the basis for the reversibility of some epilepsies. The diversity of epilepsy genes and their intervening cellular phenotypes promise to provide a rich source of novel molecular targets for therapeutic discovery and will have a lot to teach us in the future about the developmental potential of neural circuits in the mammalian brain.
Assuntos
Epilepsia/genética , Epilepsia/patologia , Regulação da Expressão Gênica/fisiologia , Plasticidade Neuronal/genética , Animais , Humanos , Camundongos , Camundongos Transgênicos , Plasticidade Neuronal/fisiologiaRESUMO
The complete coding sequence of a mouse glutamate transporter (mEAAT2) has been cloned by polymerase chain reaction (PCR) from adult whole-brain total RNA. Southern hybridization analysis of PCR products amplified from templates derived from various murine adult tissues demonstrated that the transcript for mEAAT2 was specific to the central nervous system. High-affinity transport of D-aspartate, Km value (17 +/- 5 microM), was determined in a vaccinia/T7 RNA polymerase expression system. The deduced amino-acid sequence of mEAAT2 shares 96 and 93% identity with the rat and human EAAT2 homologues, respectively.
Assuntos
Transportadores de Cassetes de Ligação de ATP/genética , Transportadores de Cassetes de Ligação de ATP/metabolismo , Sequência de Aminoácidos , Sistema X-AG de Transporte de Aminoácidos , Animais , Sequência de Bases , Encéfalo/metabolismo , Clonagem Molecular , DNA Complementar/genética , Expressão Gênica , Genes , Camundongos , Dados de Sequência Molecular , RNA Mensageiro/genética , Proteínas Recombinantes , Solubilidade , Distribuição TecidualRESUMO
Combinations of cloned GABAA receptor subtypes, having the subunit combinations alpha i + beta 1 or alpha i + beta 1 + gamma 2 (i = 1, 2, 3), were expressed in Xenopus oocytes. The endogenous steroid 3 alpha-hydroxy-5 alpha-pregnan-20-one potentiates GABA currents induced therein by GABA. This potentiation was greater in the alpha 1 + beta and alpha 3 + beta 1 than in the alpha 2 + beta 1 combinations. The presence of the gamma 2-subunit increased the steroid potency in alpha 1 + beta 1 and alpha 2 + beta 1, but the combination alpha 3 + beta 1 + gamma 2 became much less steroid-sensitive. It is concluded that the steroid modification of the GABAA receptor is strongly influenced by the alpha- and the gamma 2-subunit types.
Assuntos
Neurotransmissores/farmacologia , Pregnanolona/farmacologia , Receptores de GABA-A/efeitos dos fármacos , Xenopus/metabolismo , Animais , Clonagem Molecular , Eletrofisiologia , Expressão Gênica , Oócitos/metabolismo , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Receptores de GABA-A/química , Receptores de GABA-A/genéticaRESUMO
To determine the variability of pulsed Doppler peak velocity measurements, four radiologists with differing experience were tested using a calibrated flow phantom. Two ultrasound units, three probes and eight velocity rates varying between 40.5 and 78 cm/sec were studied, with a total of 303 measurements. The results were normalized against a set of 106 separate measurements made under highly-controlled conditions. The residual error standard deviation (not attributable to any systematically varied factor, including the velocity rate) was 6.8 cm/sec, with most of the remaining variation due to changing transducer or machine. Observer/equipment interactions accounted for 15.8% of the observed variability. The duration of the radiologist's Doppler experience had no significant effect.
Assuntos
Velocidade do Fluxo Sanguíneo , Variações Dependentes do Observador , Ultrassonografia/estatística & dados numéricos , Humanos , Modelos Cardiovasculares , Modelos Estruturais , UltrassomRESUMO
Transabdominal and endovaginal pelvic sonograms were obtained in 108 nonpregnant patients referred for pelvic sonography. The studies were independently obtained by two radiologists and interpreted on the basis of identical clinical information. The sonograms were then compared for anatomic detail and abnormalities. A determination was made about which examination, if either, was superior. Follow-up was performed through a review of the medical records and follow-up studies. Overall, the endovaginal study was judged superior in 65 cases (60.2%), equal in 39 (36.1%), and inferior in four (3.7%). The authors conclude that the endovaginal examination can effectively replace the transabdominal examination as the initial approach for routine pelvic sonography.