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1,498 result(s) for "Chen, Han-Yu"
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Achromatic metalens array for full-colour light-field imaging
A light-field camera captures both the intensity and the direction of incoming light1–5. This enables a user to refocus pictures and afterwards reconstruct information on the depth of field. Research on light-field imaging can be divided into two components: acquisition and rendering. Microlens arrays have been used for acquisition, but obtaining broadband achromatic images with no spherical aberration remains challenging. Here, we describe a metalens array made of gallium nitride (GaN) nanoantennas6 that can be used to capture light-field information and demonstrate a full-colour light-field camera devoid of chromatic aberration. The metalens array contains an array of 60 × 60 metalenses with diameters of 21.65 μm. The camera has a diffraction-limited resolution of 1.95 μm under white light illumination. The depth of every object in the scene can be reconstructed slice by slice from a series of rendered images with different depths of focus. Full-colour, achromatic light-field cameras could find applications in a variety of fields such as robotic vision, self-driving vehicles and virtual and augmented reality.A metalens array of GaN nanoantennas is used to make a full-colour achromatic light-field camera.
STAT3/LINC00671 axis regulates papillary thyroid tumor growth and metastasis via LDHA-mediated glycolysis
Lactate dehydrogenase A (LDHA), a critical component of the glycolytic pathway, relates to the development of various cancers, including thyroid cancer. However, the regulatory mechanism of LDHA inhibition and the physiological significance of the LDHA inhibitors in papillary thyroid cancer (PTC) are unknown. Long non-coding RNA (lncRNA) plays a vital role in tumor growth and progression. Here, we identified a novel lncRNA LINC00671 negatively correlated with LDHA, downregulating LDHA expression and predicting good clinical outcome in thyroid cancer. Moreover, hypoxia inhibits LINC00671 expression and activates LDHA expression largely through transcriptional factor STAT3. STAT3/LINC00671/LDHA axis regulates thyroid cancer glycolysis, growth, and lung metastasis both in vitro and in vivo. In thyroid cancer patients, LINC00671 expression is negatively correlated with LDHA and STAT3 expression. Our work established STAT3/LINC00671/LDHA as a critical axis to regulate PTC growth and progression. Inhibition of LDHA or STAT3 or supplement of LINC00671 could be potential therapeutic strategies in thyroid cancer.
Assessment of the Performance of Ultrasonography for Detecting Myofascial Trigger Points
Needle electromyogram (EMG) research has suggested that endplate noise (EPN) is a characteristic of myofascial trigger points (MTrPs). Although several studies have observed MTrPs through ultrasonography, whether they are hyperechoic or hypoechoic in ultrasound images is still controversial. Therefore, this study determined the echogenicity of MTrP ultrasonography. In stage 1, the MTrP of rat masseter muscle was identified through palpation and marked. Needle EMG was performed to detect the presence of EPN. When EPN was detected, ultrasound scans and indwelling needles were used to identify the nodule with a different grayscale relative to that of its surrounding tissue, and the echogenicity of the identified MTrP was determined. In stage 2, these steps were reversed. An ultrasound scan was performed to detect the nodule at the marked site, and an EMG needle was inserted into the nodule to detect EPN. There were 178 recordings in each stage, obtained from 45 rats. The stage 1 results indicate that the MTrPs in ultrasound images were hypoechoic with a 100% sensitivity of assessment. In stage 2, the accuracy and precision of MTrP detection through ultrasonography were 89.9% and 89.2%, respectively. The results indicate that ultrasonography produces highly accurate and precise MTrP detection results.
Single-cell sequencing of ascites fluid illustrates heterogeneity and therapy-induced evolution during gastric cancer peritoneal metastasis
Peritoneal metastasis is the leading cause of death for gastrointestinal cancers. The native and therapy-induced ascites ecosystems are not fully understood. Here, we characterize single-cell transcriptomes of 191,987 ascites cancer/immune cells from 35 patients with/without gastric cancer peritoneal metastasis (GCPM). During GCPM progression, an increase is seen of monocyte-like dendritic cells (DCs) that are pro-angiogenic with reduced antigen-presenting capacity and correlate with poor gastric cancer (GC) prognosis. We also describe the evolution of monocyte-like DCs and regulatory and proliferative T cells following therapy. Moreover, we track GC evolution, identifying high-plasticity GC clusters that exhibit a propensity to shift to a high-proliferative phenotype. Transitions occur via the recently described, autophagy-dependent plasticity program, paligenosis. Two autophagy-related genes ( MARCKS and TXNIP ) mark high-plasticity GC with poorer prognosis, and autophagy inhibitors induce apoptosis in patient-derived organoids. Our findings provide insights into the developmental trajectories of cancer/immune cells underlying GCPM progression and therapy resistance. Peritoneal metastasis is one of the most common forms of death for gastrointestinal cancers, however, its cell composition is incompletely understood. Here, the authors use single cell RNA-seq of peritoneal metastases from 35 patients and show diversity in immune cells, and plasticity in cancer cell phenotypes and autophagy related genes as biomarkers of prognosis.
Magnetoencephalography and the infant brain
Magnetoencephalography (MEG) is a non-invasive neuroimaging technique that provides whole-head measures of neural activity with millisecond temporal resolution. Over the last three decades, MEG has been used for assessing brain activity, most commonly in adults. MEG has been used less often to examine neural function during early development, in large part due to the fact that infant whole-head MEG systems have only recently been developed. In this review, an overview of infant MEG studies is provided, focusing on the period from birth to three years. The advantages of MEG for measuring neural activity in infants are highlighted (See Box 1), including the ability to assess activity in brain (source) space rather than sensor space, thus allowing direct assessment of neural generator activity. Recent advances in MEG hardware and source analysis are also discussed. As the review indicates, efforts in this area demonstrate that MEG is a promising technology for studying the infant brain. As a noninvasive technology, with emerging hardware providing the necessary sensitivity, an expected deliverable is the capability for longitudinal infant MEG studies evaluating the developmental trajectory (maturation) of neural activity. It is expected that departures from neuro-typical trajectories will offer early detection and prognosis insights in infants and toddlers at-risk for neurodevelopmental disorders, thus paving the way for early targeted interventions. •MEG provides real-time (msec) measures of neural activity in infants.•MEG signals can be modeled in source (brain) space.•MEG can detect oscillations in the infant brain – probes for connectivity.•Emerging MEG hardware provides increased sensitivity to infant brain activity.
Trait anxiety negatively modulates the coupling of motor event-related desynchronization and event-related synchronization
Background Recent neurophysiological studies showed that patients with psychiatric disorders demonstrated abnormalities in sensorimotor functions in addition to cognitive deficits. These findings intrigued us to investigate whether trait anxiety, a persistent inclination towards being anxious in multiple contexts, would affect motor cortical functions. Event-related desynchronization (ERD) and event-related synchronization (ERS) of α and β oscillations are associated with movement execution and movement termination, respectively. However, no study has comprehensively examined the effects of trait anxiety on motor ERD and ERS. Therefore, this study aimed to determine how trait anxiety influences these motor cortical oscillations. Methods Twenty subjects (top 10% of the trait anxiety score distribution from 400 college students) with higher trait anxiety (HTA) and 20 subjects (bottom 10% of trait anxiety score distribution from the same sample) with lower trait anxiety (LTA) were recruited to perform a Go-Nogo task during electroencephalographic recordings. ERD and ERS of α and β oscillations to Go responses were compared between these two groups. The associations between ERD and ERS in each group were also examined. Results Neither ERD nor ERS power changes were significantly different between LTA and HTA groups. Interestingly, a significant correlation between β ERD and α ERS/β ERS was found in the individuals with LTA; however, such functional coupling was not present in the individuals with HTA. Conclusion Trait anxiety negatively modulates the coupling of motor ERD and ERS.
A 4‐month‐old female infant with complete colonic duplication presenting with stool leaking out of the vestibule
Complete colonic duplication (Figure 1E) and double appendixes (Figure 1F) were discovered through the laparoscopy. [...]instead of excision of the duplicated colon, the patient was treated with anastomosis of the duplicated colon to the native colon (Figure 1E), alongside ligation of the fistula and resection of the duplicated appendix. Colonic and rectal duplications are rare congenital malformations, accounting for less than 20% of all enteric duplications. 1 Hindgut duplications, which include colonic and rectal duplications, can be categorized into three classes: small intra-mesenteric duplications, presacral midline masses, and side-by-side tubular duplications. CONFLICT OF INTEREST STATEMENT The authors declare no conflict of interest.