Familial influences on the full range of variability in attention and activity levels during adolescence: A longitudinal twin study

AbstractTo investigate familial influences on the full range of variability in attention and activity across adolescence, we collected maternal ratings of 339 twin pairs at ages 12, 14, and 16, and estimated the transmitted and new familial influences on attention and activity as measured by the Strengths and Weaknesses of Attention-Deficit/Hyperactivity Disorder Symptoms and Normal Behavior Scale. Familial influences were substantial for both traits across adolescence: genetic influences accounted for 54%–73% (attention) and 31%–73% (activity) of the total variance, and shared environmental influences accounted for 0%–22% of the attention variance and 13%–57% of the activity variance. The longitudinal stability of individual differences in attention and activity was largely accounted for by familial influences transmitted from previous ages. Innovations over adolescence were also partially attributable to familial influences. Studying the full range of variability in attention and activity may facilitate our understanding of attention-deficit/hyperactivity disorder's etiology and intervention.</jats:p

A Low-Power Passive UHF Tag With High-Precision Temperature Sensor for Human Body Application

Radio frequency identification (RFID) tags are widely used in various electronic devices due to their low cost, simple structure, and convenient data reading. This topic aims to study the key technologies of ultra-high frequency (UHF) RFID tags and high-precision temperature sensors, and how to reduce the power consumption of the temperature sensor and the overall circuits while maintaining minimal loss of performance. Combined with the biomedicine, an innovative high-precision human UHF RFID chip for body temperature monitoring is designed. In this study, a ring oscillator whose output frequency is linearly related to temperature is designed and proposed as a temperature-sensing circuit by innovatively combining auxiliary calibration technology. Then, a binary counter is used to count the pulses, and the temperature is ultimately calculated. This topic designed a relaxation oscillator independent of voltage and current. The various types of resistors were used to offset the temperature deviation. A current mirror array calibration circuit is used to calibrate the process corner deviation of the clock circuit with a self-calibration algorithm. This study mainly contributes to reducing power consumption and improving accuracy. The total power consumption of the RF/analog front-end and temperature sensor is 7.65µW. The measurement error of the temperature sensor in the range of 0 to 60◦C is less than ±0.1%, and the accuracy of the output frequency of the clock circuit is ±2.5%

Massive Galaxies in COSMOS: Evolution of Black hole versus bulge mass but not versus total stellar mass over the last 9 Gyrs?

We constrain the ratio of black hole (BH) mass to total stellar mass of type-1 AGN in the COSMOS survey at 1<z<2. For 10 AGN at mean redshift z~1.4 with both HST/ACS and HST/NICMOS imaging data we are able to compute total stellar mass M_(*,total), based on restframe UV-to-optical host galaxy colors which constrain mass-to-light ratios. All objects have virial BH mass-estimates available from the COSMOS Magellan/IMACS and zCOSMOS surveys. We find zero difference between the M_BH--M_(*,total)-relation at z~1.4 and the M_BH--M_(*,bulge)-relation in the local Universe. Our interpretation is: (a) If our objects were purely bulge-dominated, the M_BH--M_(*,bulge)-relation has not evolved since z~1.4. However, (b) since we have evidence for substantial disk components, the bulges of massive galaxies (logM_(*,total)=11.1+-0.25 or logM_BH~8.3+-0.2) must have grown over the last 9 Gyrs predominantly by redistribution of disk- into bulge-mass. Since all necessary stellar mass exists in the galaxy at z=1.4, no star-formation or addition of external stellar material is required, only a redistribution e.g. induced by minor and major merging or through disk instabilities. Merging, in addition to redistributing mass in the galaxy, will add both BH and stellar/bulge mass, but does not change the overall final M_BH/M_(*,bulge) ratio. Since the overall cosmic stellar and BH mass buildup trace each other tightly over time, our scenario of bulge-formation in massive galaxies is independent of any strong BH-feedback and means that the mechanism coupling BH and bulge mass until the present is very indirect.Comment: Published in ApJL; 7 pages, 2 figures; updated to accepted version (methods changed, results unchanged

Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives

The synthesis and characterisation of a homologous series of quinoid sulfur-containing imidazolyl-substituted heteroacenes is described. The optoelectronic and magnetic properties were investigated by UV/vis, fluorescence and EPR spectroscopy as well as quantum-chemical calculations, and were compared to those of the corresponding benzo congener. The room-temperature and atmospherically stable quinoids display strong absorption in the NIR region between 678 and 819 nm. The dithieno[3,2-b:2′,3′-d]thiophene and the thieno[2′,3′:4,5]thieno[3,2-b]thieno[2,3-d]thiophene derivatives were EPR active at room temperature. For the latter, variable-temperature EPR spectroscopy revealed the presence of a thermally accessible triplet state, with a singlet-triplet separation of 14.1 kJ mol$^{-1}$

Structural mechanism for gating of a eukaryotic mechanosensitive channel of small conductance

Mechanosensitive ion channels transduce physical force into electrochemical signaling that underlies an array of fundamental physiological processes, including hearing, touch, proprioception, osmoregulation, and morphogenesis. The mechanosensitive channels of small conductance (MscS) constitute a remarkably diverse superfamily of channels critical for management of osmotic pressure. Here, we present cryo-electron microscopy structures of a MscS homolog from Arabidopsis thaliana, MSL1, presumably in both the closed and open states. The heptameric MSL1 channel contains an unusual bowl-shaped transmembrane region, which is reminiscent of the evolutionarily and architecturally unrelated mechanosensitive Piezo channels. Upon channel opening, the curved transmembrane domain of MSL1 flattens and expands. Our structures, in combination with functional analyses, delineate a structural mechanism by which mechanosensitive channels open under increased membrane tension. Further, the shared structural feature between unrelated channels suggests the possibility of a unified mechanical gating mechanism stemming from membrane deformation induced by a non-planar transmembrane domain

Clinical trial-identified inflammatory biomarkers in breast and pancreatic cancers

Breast cancer and pancreatic cancer are two common cancer types characterized by high prevalence and high mortality rates, respectively. However, breast cancer has been more well-studied than pancreatic cancer. This narrative review curated inflammation-associated biomarkers from clinical studies that were systematically selected for both breast and pancreatic cancers and discusses some of the common and unique elements between the two endocrine-regulated malignant diseases. Finding common ground between the two cancer types and specifically analyzing breast cancer study results, we hoped to explore potential feasible methods and biomarkers that may be useful also in diagnosing and treating pancreatic cancer. A PubMed MEDLINE search was used to identify articles that were published between 2015-2022 of different kinds of clinical trials that measured immune-modulatory biomarkers and biomarker changes of inflammation defined in diagnosis and treatment of breast cancer and pancreatic cancer patients. A total of 105 papers (pancreatic cancer 23, breast cancer 82) were input into Covidence for the title and abstract screening. The final number of articles included in this review was 73 (pancreatic cancer 19, breast cancer 54). The results showed some of the frequently cited inflammatory biomarkers for breast and pancreatic cancers included IL-6, IL-8, CCL2, CD8+ T cells and VEGF. Regarding unique markers, CA15-3 and TNF-alpha were two of several breast cancer-specific, and CA19 and IL-18 were pancreatic cancer-specific. Moreover, we discussed leptin and MMPs as emerging biomarker targets with potential use for managing pancreatic cancer based on breast cancer studies in the future, based on inflammatory mechanisms. Overall, the similarity in how both types of cancers respond to or result in further disruptive inflammatory signaling, and that point to a list of markers that have been shown useful in diagnosis and/or treatment method response or efficacy in managing breast cancer could potentially provide insights into developing the same or more useful diagnostic and treatment measurement inflammatory biomarkers for pancreatic cancer. More research is needed to investigate the relationship and associated inflammatory markers between the similar immune-associated biological mechanisms that contribute to breast and pancreatic cancer etiology, drive disease progression or that impact treatment response and reflect survival outcomes