62 research outputs found
Single ion implantation for single donor devices using Geiger mode detectors
Electronic devices that are designed to use the properties of single atoms
such as donors or defects have become a reality with recent demonstrations of
donor spectroscopy, single photon emission sources, and magnetic imaging using
defect centers in diamond. Improving single ion detector sensitivity is linked
to improving control over the straggle of the ion as well as providing more
flexibility in lay-out integration with the active region of the single donor
device construction zone by allowing ion sensing at potentially greater
distances. Using a remotely located passively gated single ion Geiger mode
avalanche diode (SIGMA) detector we have demonstrated 100% detection efficiency
at a distance of >75 um from the center of the collecting junction. This
detection efficiency is achieved with sensitivity to ~600 or fewer
electron-hole pairs produced by the implanted ion. Ion detectors with this
sensitivity and integrated with a thin dielectric, for example 5 nm gate oxide,
using low energy Sb implantation would have an end of range straggle of <2.5
nm. Significant reduction in false count probability is achieved by modifying
the ion beam set-up to allow for cryogenic operation of the SIGMA detector.
Using a detection window of 230 ns at 1 Hz, the probability of a false count
was measured as 1E-1 and 1E-4 for operation temperatures of 300K and 77K,
respectively. Low temperature operation and reduced false, dark, counts are
critical to achieving high confidence in single ion arrival. For the device
performance in this work, the confidence is calculated as a probability of >98%
for counting one and only one ion for a false count probability of 1E-4 at an
average ion number per gated window of 0.015.Comment: 10 pages, 5 figures, submitted to Nanotechnolog
Gender discrepancy in research activities during radiology residency
Objective: To investigate the presence of gender disparity in academic involvement during radiology residency and to identify and characterize any gender differences in perceived barriers for conducting research. / Methods: An international call for participation in an online survey was promoted via social media and through multiple international and national radiological societies. A 35-question survey invited radiology trainees worldwide to answer questions regarding exposure and barriers to academic radiology during their training. Gender differences in response proportions were analyzed using either Fisher’s exact or chi-squared tests. / Results: Eight hundred fifty-eight participants (438 men, 420 women) from Europe (432), Asia (241), North and South America (144), Africa (37), and Oceania (4) completed the survey. Fewer women radiology residents were involved in research during residency (44.3%, 186/420 vs 59.4%, 260/438; p ≤ 0.0001) and had fewer published original articles (27.9%, 117/420 vs. 40.2%, 176/438; p = 0.001). Women were more likely to declare gender as a barrier to research (24.3%, 102/420 vs. 6.8%, 30/438; p < 0.0001) and lacked mentorship/support from faculty (65%, 273/420 vs. 55.7%, 244/438; p = 0.0055). Men were more likely to declare a lack of time (60.3%, 264/438 vs. 50.7%, 213/420; p = 0.0049) and lack of personal interest (21%, 92/438 vs. 13.6%, 57/420, p = 0.0041) in conducting research. / Conclusion: Fewer women were involved in academic activities during radiology residency, resulting in fewer original published studies compared to their men counterparts. This is indicative of an inherent gender imbalance. Lack of mentorship reported by women radiologists was a main barrier to research
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Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice.
Pathogenic variants in KMT5B, a lysine methyltransferase, are associated with global developmental delay, macrocephaly, autism, and congenital anomalies (OMIM# 617788). Given the relatively recent discovery of this disorder, it has not been fully characterized. Deep phenotyping of the largest (n = 43) patient cohort to date identified that hypotonia and congenital heart defects are prominent features that were previously not associated with this syndrome. Both missense variants and putative loss-of-function variants resulted in slow growth in patient-derived cell lines. KMT5B homozygous knockout mice were smaller in size than their wild-type littermates but did not have significantly smaller brains, suggesting relative macrocephaly, also noted as a prominent clinical feature. RNA sequencing of patient lymphoblasts and Kmt5b haploinsufficient mouse brains identified differentially expressed pathways associated with nervous system development and function including axon guidance signaling. Overall, we identified additional pathogenic variants and clinical features in KMT5B-related neurodevelopmental disorder and provide insights into the molecular mechanisms of the disorder using multiple model systems
Hand osteoarthritis: clinical phenotypes, molecular mechanisms and disease management
Osteoarthritis (OA) is a highly prevalent condition and the hand is the most commonly affected site. Patients with hand OA frequently report symptoms of pain, functional limitations, and frustration in undertaking everyday activities. The condition presents clinically with changes to the bone, ligaments, cartilage and synovial tissue, which can be observed using radiography, ultrasonography or MRI. Hand OA is a heterogeneous disorder and is considered to be multifactorial in aetiology. This review provides an overview of the epidemiology, presentation and burden of hand OA, including an update on hand OA imaging (including the development of novel techniques), disease mechanisms and management. In particular, areas for which new evidence has substantially changed the way we understand, consider and treat hand OA are highlighted. For example, genetic studies, clinical trials and careful prospective imaging studies from the past 5 years are beginning to provide insights into the pathogenesis of hand OA that might uncover new therapeutic targets in disease
4x4 Individually Addressable InGaAs APD Arrays Optimized for Photon Counting Applications
InGaAs APDs with improved photon counting characteristics were designed and fabricated and their performance improvements were observed. Following the results, a 4x4 individually addressable APD array was designed, fabricated, and results are reported
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