Results 41 to 50 of about 6,229,843 (307)

Characterizations of GEM detector prototype

open access: yes, 2015
At NISER-IoP detector laboratory an initiative is taken to build and test Gas Electron Multiplier (GEM) detectors for ALICE experiment. The optimisation of the gas flow rate and the long-term stability test of the GEM detector are performed.
Bhattacharya, P.   +9 more
core   +3 more sources

Outcomes of Live Virus Vaccination in Patients With Vascular Anomalies Being Treated With Sirolimus

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Live vaccination in patients with vascular anomalies (VA) receiving sirolimus remains controversial due to immunosuppressive effects and theoretical risks. Procedure This single‐center retrospective study included patients with VA less than 4 years old at the start of sirolimus therapy who were incompletely vaccinated.
Svatava Merkle   +5 more
wiley   +1 more source

Roll angle measurement system based on triaxial magneto-resistive sensor

open access: yesJournal of Measurement Science and Instrumentation, 2013
Aiming at large error when inertial devices measure the roll angle under high overload conditions,the article designs one kind of roll angle measurement system based on magneto-resistive sensor which calculates the roll angle by micro controller STM32 ...
ZHAO Xin-lu   +4 more
doaj  

Synergistic Enhancement Properties of a Flexible Integrated PAN/PVDF Piezoelectric Sensor for Human Posture Recognition

open access: yesNanomaterials, 2022
The flexible pressure sensor has attracted much attention due to its wearable and conformal advantage. All the same, enhancing its electrical and structural properties is still a huge challenge.
Jiliang Mu   +8 more
doaj   +1 more source

NRASQ61R Expression in Lymphatic Endothelial Cells Causes Enlarged Vessels, Hemorrhagic Chylous Effusions, and High Mortality in a Mouse Model of Kaposiform Lymphangiomatosis

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Kaposiform lymphangiomatosis (KLA) is an aggressive complex lymphatic anomaly. Patients exhibit malformed lymphatic vessels and often develop hemorrhagic effusions and elevated angiopoietin‐2 (Ang‐2) levels. A somatic NRAS p.Q61R (NRASQ61R) mutation has been associated with KLA.
C. Griffin McDaniel   +3 more
wiley   +1 more source

Generation of Excel report in special spring testing system based on LabWindows /CVI

open access: yesJournal of Measurement Science and Instrumentation, 2014
This paper proposes a new method that can access the Microsoft Excel 2003 by ActiveX to make up for the limitation of the data report in LabWindows /CVI.
JIN Lu   +5 more
doaj  

A high-sensitivity flexible bionic tentacle sensor for multidimensional force sensing and autonomous obstacle avoidance applications

open access: yesMicrosystems & Nanoengineering
Bionic tentacle sensors are important in various fields, including obstacle avoidance, human‒machine interfaces, and soft robotics. However, most traditional tentacle sensors are based on rigid substrates, resulting in difficulty in detecting ...
Xinyu Liu   +12 more
doaj   +1 more source

Laboratory Technical Supplement for the Mayer-Salovey-Caruso Emotional Intelligence Test (MSCEIT) [PDF]

open access: yes, 2012
The Mayer-Salovey-Caruso Emotional Intelligence Test (MSCEIT) User’s Manual (Mayer, Salovey & Caruso, 2002), published by MHS, provides a great deal of information about using the MSCEIT test.
Mayer, John D.
core   +1 more source

Germline TP53 Mutations Causing Diamond–Blackfan Anemia: A French Report

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Diamond–Blackfan anemia is a rare congenital erythroblastopenia typically caused by mutations in ribosomal protein genes. Recently, gain‐of‐function mutations in TP53 have been identified as a novel cause of Diamond–Blackfan anemia. We report two French patients who both harbored a heterozygous TP53 deletion (NM_000546.5: c.1077delA; p ...
Rafael Moisan   +6 more
wiley   +1 more source

Targeted long-read sequencing identifies missing pathogenic variant in unsolved 11β-hydroxylase deficiency

open access: yesBMC Endocrine Disorders
Background 11β-hydroxylase deficiency (11β-OHD), caused by homozygosity or compound heterozygosity CYP11B1 variants, is the second most common cause of congenital adrenal hyperplasia (CAH).
Jidong Liu   +8 more
doaj   +1 more source

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