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1.
Opt Express ; 32(2): 1305-1313, 2024 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-38297685

RESUMO

We present a study of homodyne measurements of two-mode, vacuum-seeded, quadrature-squeezed light generated by four-wave mixing in warm rubidium vapor. Our results reveal that the vacuum squeezing can extend down to measurement frequencies of less than 1 Hz, and the squeezing bandwidth, similar to the seeded intensity-difference squeezing measured in this system, reaches up to approximately 20 MHz for typical pump parameters. By dividing the squeezing bandwidth into smaller frequency bins, we show that different sideband frequencies represent independent sources of two-mode squeezing. These properties are useful for quantum sensing and quantum information processing applications. We also investigate the impact of group velocity delays on the correlations in the system, which allows us to optimize the useful spectrum.

2.
Phytopathology ; 114(3): 500-502, 2024 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-37750871

RESUMO

The strains in Lysobacter spp. have the potential to control plant-parasitic nematodes. In our experiment, L. gummosus YMF3.00690 showed antagonistic effects against plant root-knot nematode. Nine metabolites were isolated and identified from cultures of L. gummosus YMF3.00690, of which compound 1 was identified as a new metabolite tetrahydro-4,4,6-trimethyl-6-[(tetrahydro-6,6-dimethyl-2-oxo-4(1H)-pyrimidinylidene) methyl]-2(1H)-pyrimidinone. The activity assay showed that two compounds, 5-(hydroxymethyl)-1H-pyrrole-2-carbaldehyde (2) and 1H-pyrrole-2-carboxylic acid (3), had nematicidal activities against Meloidogyne javanica with mortalities of 69.93 and 90.54% at 400 ppm for 96 h, respectively. These two compounds were further tested for the inhibition activity of eggs hatching, and compound 3 showed a significant inhibition rate of 63.36% at 50 ppm for 48 h. In the chemotactic activity assay, three compounds (1 to 3) were found to have concentration-dependent chemotactic activity, of which compound 1 showed attractive activity. This experiment explored the active metabolites of L. gummosus YMF3.00690 against M. javanica and laid the foundation for biopesticide development.


Assuntos
Lysobacter , Tylenchoidea , Animais , Tylenchoidea/fisiologia , Doenças das Plantas/prevenção & controle , Doenças das Plantas/parasitologia , Antinematódeos/farmacologia
3.
ACS Appl Mater Interfaces ; 15(36): 42170-42181, 2023 Sep 13.
Artigo em Inglês | MEDLINE | ID: mdl-37654059

RESUMO

Magnetic-assisted DNA testing technology has attracted much attention in genetics, clinical diagnostics, environmental microbiology, and molecular biology. However, achieving satisfying DNA adsorption and desorption efficiency in real samples is still a big challenge. In this paper, a new kind of high-quality magnetic composite microsphere of MM@PGMA-PA-Ti4+ was designed and prepared for DNA extraction and detection based on the strong interaction of Ti4+ and phosphate groups. By taking the advantages of high magnetic susceptibility and high Ti4+ content, the MM@PGMA-PA-Ti4+ microspheres possessed remarkable extraction capacity for mimic biological samples (salmon sperm specimens) with saturated loadings up to 533.0 mg/g. When the DNA feeding amount was 100 µg and the MM@PGMA-PA-Ti4+ dosage was 1 mg, the adsorption and desorption efficiencies were 80 and 90%, respectively. The kinetic and equilibrium extraction data were found to fit well with the pseudo-second-order model and Freundlich isotherm model. Furthermore, the MM@PGMA-PA-Ti4+ microspheres were successfully employed for DNA extraction from mouse epithelial-like fibroblasts. The extraction ability (84 ± 4 µg/mg) and DNA purity were superior to the comparative commercial spin kits, as evaluated by electrophoresis assays and qPCR analysis. The experimental results suggest that the MM@PGMA-PA-Ti4+ microspheres possess great potential as an adsorbent for DNA purification from complex biological samples.


Assuntos
Sêmen , Titânio , Masculino , Animais , Camundongos , Microesferas , Cátions , Fenômenos Magnéticos
4.
Anal Chem ; 94(28): 10151-10158, 2022 07 19.
Artigo em Inglês | MEDLINE | ID: mdl-35794045

RESUMO

Surface-enhanced Raman spectroscopy (SERS), providing near-single-molecule-level fingerprint information, is a powerful tool for the trace analysis of a target in a complicated matrix and is especially facilitated by the development of modern machine learning algorithms. However, both the high demand of mass data and the low interpretability of the mysterious black-box operation significantly limit the well-trained model to real systems in practical applications. Aiming at these two issues, we constructed a novel machine learning algorithm-based framework (Vis-CAD), integrating visual random forest, characteristic amplifier, and data augmentation. The introduction of data augmentation significantly reduced the requirement of mass data, and the visualization of the random forest clearly presented the captured features, by which one was able to determine the reliability of the algorithm. Taking the trace analysis of individual polycyclic aromatic hydrocarbons in a mixture as an example, a trustworthy accuracy no less than 99% was realized under the optimized condition. The visualization of the algorithm framework distinctly demonstrated that the captured feature was well correlated to the characteristic Raman peaks of each individual. Furthermore, the sensitivity toward the trace individual could be improved by least 1 order of magnitude as compared to that with the naked eye. The proposed algorithm distinguished by the lesser demand of mass data and the visualization of the operation process offers a new way for the indestructible application of machine learning algorithms, which would bring push-to-the-limit sensitivity toward the qualitative and quantitative analysis of trace targets, not only in the field of SERS, but also in the much wider spectroscopy world. It is implemented in the Python programming language and is open-source at https://github.com/3331822w/Vis-CAD.


Assuntos
Aprendizado de Máquina , Hidrocarbonetos Policíclicos Aromáticos , Algoritmos , Reprodutibilidade dos Testes , Análise Espectral Raman/métodos
5.
Rev Sci Instrum ; 92(10): 104102, 2021 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-34717398

RESUMO

The qualitative and quantitative analysis of polycyclic aromatic hydrocarbons (PAHs) has been important for the environmental control of persistent organic pollutants for decades. Considering the potential risk of deterioration, degradation, and external pollution during transportation, the development of rapid and onsite detection of trace PAHs is in demand. Here, taking the advantage of high sensitivity of surface-enhanced Raman spectroscopy (SERS), we developed a shipboard instrument by combining a portable Raman instrument and a flow injection device, integrating the sample pretreatment and target detection step by step. The feasibility of the instrument was demonstrated by detecting trace benzo[a]pyrene from different water environments with the lowest detection concentration less than 1 µg/l. The reliable stability and repeatability indicate that in the case of emergency response, the developed flow injection analysis-SERS instrument is very promising for the quantitative and qualitative analysis of diverse organic pollutants other than PAHs in water environments.

6.
Anal Chem ; 93(24): 8408-8413, 2021 06 22.
Artigo em Inglês | MEDLINE | ID: mdl-34110787

RESUMO

In spectroscopic analysis, push-to-the-limit sensitivity is one of the important topics, particularly when facing the qualitative and quantitative analyses of the trace target. Normally, the effective recognition and extraction of weak signals are the first key steps, for which there has been considerable effort in developing various denoising algorithms for decades. Nevertheless, the lower the signal-to-noise ratio (SNR), the greater the deviation of the peak height and shape during the denoising process. Therefore, we propose a denoising algorithm along with peak extraction and retention (PEER). First, both the first and second derivatives of the Raman spectrum are used to determine Raman peaks with a high SNR whose peak information is kept away from the denoising process. Second, an optimized window smoothing algorithm is applied to the left part of the Raman spectrum, which is combined with the untreated Raman peaks to obtain the denoised Raman spectrum. The PEER algorithm is demonstrated with much better signal extraction and retention and successfully improves the temporal resolution of Raman imaging of a living cell by at least 1 order of magnitude higher than those by traditional algorithms.


Assuntos
Algoritmos , Análise Espectral Raman , Razão Sinal-Ruído
7.
Sci Adv ; 7(22)2021 May.
Artigo em Inglês | MEDLINE | ID: mdl-34049876

RESUMO

The Stern-Gerlach effect, found a century ago, has become a paradigm of quantum mechanics. Unexpectedly, until recently, there has been little evidence that the original scheme with freely propagating atoms exposed to gradients from macroscopic magnets is a fully coherent quantum process. Several theoretical studies have explained why a Stern-Gerlach interferometer is a formidable challenge. Here, we provide a detailed account of the realization of a full-loop Stern-Gerlach interferometer for single atoms and use the acquired understanding to show how this setup may be used to realize an interferometer for macroscopic objects doped with a single spin. Such a realization would open the door to a new era of fundamental probes, including the realization of previously inaccessible tests at the interface of quantum mechanics and gravity.

8.
Angew Chem Int Ed Engl ; 60(27): 15080-15086, 2021 Jun 25.
Artigo em Inglês | MEDLINE | ID: mdl-33860594

RESUMO

Spontaneous deracemization has been used to separate homochiral domains from the racemic system. However, homochirality can only be referred to when the scales of these domains and systems are specified. To clarify this, we report self-assembly of racemates of dissymmetric cages DC-1 with a cone-shape propeller geometry, forming a centrosymmetric columnar crystalline phase (racemic at crystallographic level). Owing to their anisotropic geometry, the two enantiomers are packed in a frustrated fashion in this crystalline phase; single-handed double helices are observed (single-handedness at supramolecular level). The frustrated packing (layer continuity break-up) in turn facilitates screw dislocation during the crystal growth, forming left- or right-handed spiral platelets (symmetry-breaking at morphological level), although each platelet is composed of DC-1 racemates. The symmetry correlation between DC-1 molecules, the crystalline phase and spiral platelets, all exhibit C3 symmetry.

9.
Parkinsonism Relat Disord ; 80: 65-72, 2020 11.
Artigo em Inglês | MEDLINE | ID: mdl-32961396

RESUMO

INTRODUCTION: Genetic inheritance plays key roles in patients with ataxia and/or spastic paraplegia in consanguineous families. This study aims to clarify the genetic spectrum of patients with autosomal recessive hereditary ataxia and spastic paraplegias (AR-HA/HSPs) in consanguineous families. METHODS: A total of 36 AR-HA/HSPs consanguineous pedigrees from China were recruited into this study. Next generation sequencing (NGS), guided by homozygosity mapping (HM), was applied to identify the pathogenic variants in known genes or novel candidate genes. RESULTS: We totally made molecular diagnosis in 47.2% (17/36) of AR-HA/HSPs families. Among them, 13 AR-HAs carried pathogenic variants in SETX (n = 4), SACS (n = 2), STUB1, HSD17B4, NEU1, ADCK3, TPP1, PLA2G6 and MTCL1, while four AR-HSPs carried pathogenic variants in SPG11, ZFYVE26, ATP13A2 and ABCD1. One homozygous nonsense mutation in MRPS27 was identified in an AR-HA family, which was potentially a novel candidate gene of AR-HA. CONCLUSION: HM and NGS can serve as an efficient molecular diagnostic tool for AR-HA/HSPs in consanguineous families. Our findings provide a better understanding of genetic architecture of AR-HA/HSPs in consanguinity and broaden the clinical-genetic spectrum of the disease.


Assuntos
Consanguinidade , Paraplegia Espástica Hereditária/diagnóstico , Paraplegia Espástica Hereditária/genética , Degenerações Espinocerebelares/diagnóstico , Degenerações Espinocerebelares/genética , Adulto , Pré-Escolar , China , Mapeamento Cromossômico , DNA Helicases/genética , Feminino , Testes Genéticos , Sequenciamento de Nucleotídeos em Larga Escala , Homozigoto , Humanos , Masculino , Pessoa de Meia-Idade , Proteínas Mitocondriais/genética , Enzimas Multifuncionais/genética , Linhagem , RNA Helicases/genética , Proteínas Ribossômicas/genética , Tripeptidil-Peptidase 1 , Adulto Jovem
10.
Sci Adv ; 6(9): eaay8345, 2020 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-32158945

RESUMO

The geometric phase due to the evolution of the Hamiltonian is a central concept in quantum physics and may become advantageous for quantum technology. In noncyclic evolutions, a proposition relates the geometric phase to the area bounded by the phase-space trajectory and the shortest geodesic connecting its end points. The experimental demonstration of this geodesic rule proposition in different systems is of great interest, especially due to the potential use in quantum technology. Here, we report a previously unshown experimental confirmation of the geodesic rule for a noncyclic geometric phase by means of a spatial SU(2) matter-wave interferometer, demonstrating, with high precision, the predicted phase sign change and π jumps. We show the connection between our results and the Pancharatnam phase. Last, we point out that the geodesic rule may be applied to obtain the red shift in general relativity, enabling a new quantum tool to measure gravity.

11.
Spectrochim Acta A Mol Biomol Spectrosc ; 234: 118250, 2020 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-32197231

RESUMO

Polycyclic aromatic hydrocarbons (PAHs) are among the most hazardous pollutants and have attracted significant attention in the last decades. Up to now, rapid and on-site trace detection of PAHs remains a challenging issue. Here, taking advantage of the high sensitivity and reliable qualification of Surface-enhanced Raman Spectroscopy (SERS), we firstly carried out trace analyses of 16 typical PAHs in water at concentrations as low as 100-0.1 µg/L, depending on the number of aromatic rings of the molecule. Furthermore, owing to the simplicity of the liquid-liquid extraction (LLE) step, the sensitivity was further improved 2-3 orders of magnitude, and the lowest detectable concentrations were 100, 50, and 5 ng/L for anthracene, pyrene, and benzo[a]pyrene (the three PAHs typically found in heavily polluted waters), respectively. The LLE-SERS approach was successfully applied to the qualitative and quantitative analyses of different (ocean and coast) water samples being spiked by these three PAHs, which showed great promise as a trace detection tool of PAHs under water environments having different contaminant matrices.

12.
FEBS Open Bio ; 9(6): 1119-1127, 2019 06.
Artigo em Inglês | MEDLINE | ID: mdl-30985981

RESUMO

Cystic fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. CF cells and tissues exhibit various mitochondrial abnormalities. However, the underlying molecular mechanisms remain elusive. Here, we examined the mechanisms through which CFTR regulates Bcl-2 family proteins, which in turn regulate permeabilization of the mitochondrial outer membrane. Notably, inhibition of CFTR activated Bax and Bad, but inhibited Bcl-2. Moreover, degradation of phosphorylated extracellular signal-regulated kinase 1/2 (ERK1/2) and AKT increased significantly in CFTR-knockdown cells. Dysfunction of CFTR decreased heat-shock protein 90 (Hsp90) mRNA levels, and CFTR was found to interact with Hsp90. Inhibition of Hsp90 by SNX-2112 induced the degradation of phosphorylated AKT and ERK1/2 in Caco2 and HRT18 cells. These findings may help provide insights into the physiological role of CFTR in CF-related diseases.


Assuntos
Neoplasias Colorretais/metabolismo , Regulador de Condutância Transmembrana em Fibrose Cística/genética , Regulador de Condutância Transmembrana em Fibrose Cística/metabolismo , Proteínas de Choque Térmico HSP90/metabolismo , Sistema de Sinalização das MAP Quinases , Proteínas Proto-Oncogênicas c-akt/metabolismo , Células CACO-2 , Neoplasias Colorretais/patologia , Fibrose Cística/genética , Técnicas de Silenciamento de Genes , Proteínas de Choque Térmico HSP90/antagonistas & inibidores , Proteínas de Choque Térmico HSP90/genética , Compostos Heterocíclicos de 4 ou mais Anéis/farmacologia , Humanos , Mitocôndrias/metabolismo , Fosforilação , Proteólise/efeitos dos fármacos , Proteínas Proto-Oncogênicas c-bcl-2/genética , Proteínas Proto-Oncogênicas c-bcl-2/metabolismo , Transdução Genética , Regulação para Cima/genética , Proteína X Associada a bcl-2/genética , Proteína X Associada a bcl-2/metabolismo , Proteína de Morte Celular Associada a bcl/genética , Proteína de Morte Celular Associada a bcl/metabolismo
13.
Cell Biol Int ; 43(6): 642-650, 2019 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-30958600

RESUMO

Most traditional cytotoxic chemotherapeutic agents have poor aqueous solubility and significant toxicity. Hence, there is a need to develop molecule-targeted drugs. Programmed death-ligand 1 (PD-L1) is associated with the prognosis of several cancer types, and blockade of PD-1/PD-L1 signaling increases the amplitude of anti-tumor immunity. In the present study, we investigated the effects of JQ1, a bromodomain and extraterminal-bromodomain inhibitor, on cell growth, and messenger RNA (mRNA) and protein levels of PD-L1 in renal cell carcinoma primary culture cells, and prostate, liver, and lung cancer cell lines. The results of the cell counting kit-8 assay suggested that JQ1 inhibits cell growth in a dose-dependent manner. The mRNA and protein levels of PD-L1 decreased in the primary culture of JQ1-treated renal carcinoma, prostate cancer, liver cancer, and lung cancer cell lines. In addition, the mRNA level of PD-L2 also decreased in the JQ1-treated cells. Overall, JQ1 might be a potential anti-tumor agent.


Assuntos
Azepinas/farmacologia , Antígeno B7-H1/antagonistas & inibidores , Carcinoma de Células Renais/metabolismo , Neoplasias/tratamento farmacológico , Triazóis/farmacologia , Azepinas/metabolismo , Antígeno B7-H1/biossíntese , Antígeno B7-H1/genética , Carcinoma de Células Renais/genética , Ciclo Celular/efeitos dos fármacos , Linhagem Celular Tumoral/efeitos dos fármacos , Proliferação de Células/efeitos dos fármacos , Expressão Gênica/efeitos dos fármacos , Humanos , Neoplasias/genética , Neoplasias/metabolismo , Cultura Primária de Células , RNA Mensageiro , Transdução de Sinais/efeitos dos fármacos , Triazóis/metabolismo
14.
Front Oncol ; 9: 1447, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31921692

RESUMO

Breast cancer is the leading cause of cancer-related deaths in women; however, its underlying etiology remains largely unknown. In this study, we systematically analyzed breast cancer tissues using comprehensive iTRAQ labeled quantitative proteomics, identifying 841 differentially expressed proteins (474 and 367 significantly over- and under-expressed, respectively), which were annotated by protein domain analysis. All the heat shock proteins identified were upregulated in breast cancer tissues; Hsp90 upregulation was also validated by RT-qPCR and immunohistochemistry, and high Hsp90 protein levels correlated with poorer survival. Hsp90AA1 overexpression promoted MDA-MB-231 cell proliferation, whilst BJ-B11, an Hsp90 inhibitor, hampered their invasion, migration, and proliferation in a time and dose-dependent manner and induced cell cycle arrest and apoptosis. BJ-B11 inhibited the expression of epithelial-mesenchymal transition (EMT) marker in MDA-MB-231 cells, whereas Hsp90AA1 promoted its expression. Moreover, BJ-B11 inhibited tumor growth in xenograft model. Altogether, Hsp90 activation is a risk factor in breast cancer patients, and BJ-B11 could be used to treat breast cancer.

16.
Front Neurol ; 8: 714, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29312133

RESUMO

OBJECTIVE: Spinocerebellar ataxia type 3 (SCA3) is the most commonly occurring type of autosomal dominant spinocerebellar ataxia. The present study aims to investigate progressive changes in white matter (WM) fiber in asymptomatic and symptomatic patients with SCA3. METHODS: A total of 62 participants were included in this study. Among them, 16 were asymptomatic mutation carriers (pre-SCA3), 22 were SCA3 patients with clinical symptoms, and 24 were normal controls (NC). Group comparison of tract-based spatial statistics was performed to identify microstructural abnormalities at different SCA3 disease stages. RESULTS: Decreased fractional anisotropy (FA) and increased mean diffusivity (MD) were found in the left inferior cerebellar peduncle and superior cerebellar peduncle (SCP) in the pre-SCA3 group compared with NC. The symptomatic SCA3 group showed brain-wide WM tracts impairment in both supratentorial and infratentorial networks, and the mean FA value of the WM skeleton showed a significantly negative correlation with the International Cooperative Ataxia Rating Scale (ICARS) scores. Specifically, FA of the bilateral posterior limb of the internal capsule negatively correlated with SCA3 disease duration. We also found that FA values in the right medial lemniscus and SCP negatively correlated with ICARS scores, whereas FA in the right posterior thalamic radiation positively correlated with Montreal Cognitive Assessment scores. In addition, MD in the middle cerebellar peduncle, left anterior limb of internal capsule, external capsule, and superior corona radiate positively correlated with ICARS scores in SCA3 patients. CONCLUSION: WM microstructural changes are present even in the asymptomatic stages of SCA3. In individuals in which the disease has progressed to the symptomatic stage, the integrity of WM fibers across the whole brain is affected. Furthermore, abnormalities in WM tracts are closely related to SCA3 disease severity, including movement disorder and cognitive dysfunction. These findings can deepen our understanding of the neural basis of SCA3 dysfunction.

17.
Sci Rep ; 6: 32478, 2016 09 08.
Artigo em Inglês | MEDLINE | ID: mdl-27604643

RESUMO

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease affecting motor neurons of the brain, brainstem and spinal cord. To date, mutations in more than 30 genes have been linked to the pathogenesis of ALS. Among them, SOD1, FUS and TARDBP are ranked as the three most common genes associated with ALS. However, no mutation analysis has been reported in central-southern China. In this study, we sequenced SOD1, FUS and TARDBP in a central-southern Chinese cohort of 173 patients with ALS (15 familial ALS and 158 sporadic ALS) to detect mutations. As a result, five missense mutations in SOD1, namely, p.D101N, p.D101G, p.C111Y, p.N86S and p.V87A, were identified in three unrelated familial probands and three sporadic cases; two mutations in FUS were found in two unrelated familial probands, including an insertion mutation (p.P525_Y526insY) and a missense mutation (p.R521H); no variants of TARDBP were observed in patients. Therefore, SOD1 mutations were present in 20.0% of familial ALS patients and 1.9% of sporadic ALS patients, while FUS mutations were responsible for 13.3% of familial ALS cases, and TARDBP mutations were rare in either familial or sporadic ALS cases. This study broadens the known mutational spectrum in patients with ALS and further demonstrates the necessity for genetic screening in ALS patients from central-southern China.


Assuntos
Esclerose Lateral Amiotrófica/genética , Proteínas de Ligação a DNA/genética , Predisposição Genética para Doença , Mutação , Proteína FUS de Ligação a RNA/genética , Superóxido Dismutase-1/genética , Adulto , Idoso , Esclerose Lateral Amiotrófica/classificação , Esclerose Lateral Amiotrófica/etnologia , Esclerose Lateral Amiotrófica/patologia , Sequência de Bases , China , Estudos de Coortes , Análise Mutacional de DNA , Éxons , Feminino , Expressão Gênica , Testes Genéticos , Humanos , Masculino , Pessoa de Meia-Idade , Linhagem
19.
Sci Rep ; 6: 24327, 2016 Apr 13.
Artigo em Inglês | MEDLINE | ID: mdl-27071546

RESUMO

Schizophrenia (SCZ) is a serious psychiatric disease with strong heritability. Its complexity is reflected by extensive genetic heterogeneity and much of the genetic liability remains unaccounted for. We applied a combined strategy involving detection of copy number variants (CNVs), whole-genome mapping, and exome sequencing to identify the genetic basis of autosomal-dominant SCZ in a Chinese family. To rule out pathogenic CNVs, we first performed Illumina single nucleotide polymorphism (SNP) array analysis on samples from two patients and one psychiatrically healthy family member, but no pathogenic CNVs were detected. In order to further narrow down the susceptible region, we conducted genome-wide linkage analysis and mapped the disease locus to chromosome 7q21.13-22.3, with a maximum multipoint logarithm of odds score of 2.144. Whole-exome sequencing was then carried out with samples from three affected individuals and one unaffected individual in the family. A missense variation c.9575 C > G (p.Thr3192Ser) was identified in RELN, which is known as a risk gene for SCZ, located on chromosome 7q22, in the pedigree. This rare variant, as a highly penetrant risk variant, co-segregated with the phenotype. Our results provide genetic evidence that RELN may be one of pathogenic gene in SCZ.


Assuntos
Moléculas de Adesão Celular Neuronais/genética , Variações do Número de Cópias de DNA , Proteínas da Matriz Extracelular/genética , Proteínas do Tecido Nervoso/genética , Esquizofrenia/genética , Serina Endopeptidases/genética , Adulto , Sequência de Aminoácidos , Animais , China , Feminino , Ligação Genética , Humanos , Masculino , Pessoa de Meia-Idade , Mutação de Sentido Incorreto , Linhagem , Proteína Reelina , Homologia de Sequência de Aminoácidos
20.
Science ; 349(6253): 1205-8, 2015 Sep 11.
Artigo em Inglês | MEDLINE | ID: mdl-26249229

RESUMO

In Einstein's general theory of relativity, time depends locally on gravity; in standard quantum theory, time is global-all clocks "tick" uniformly. We demonstrate a new tool for investigating time in the overlap of these two theories: a self-interfering clock, comprising two atomic spin states. We prepare the clock in a spatial superposition of quantum wave packets, which evolve coherently along two paths into a stable interference pattern. If we make the clock wave packets "tick" at different rates, to simulate a gravitational time lag, the clock time along each path yields "which path" information, degrading the pattern's visibility. In contrast, in standard interferometry, time cannot yield "which path" information. This proof-of-principle experiment may have implications for the study of time and general relativity and their impact on fundamental effects such as decoherence and the emergence of a classical world.

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