Results 181 to 190 of about 10,774 (209)
Some of the next articles are maybe not open access.

Biallelic variants in TNR cause neurodevelopmental disorders with variable expressivity

Journal of Human Genetics
Tenascin-R (TNR) is an extracellular matrix glycoprotein that is essential for the formation of perineuronal nets in the central nervous system and is critical for neurite outgrowth, synaptic plasticity, and neural stem cell proliferation and differentiation.
Atsuhiro Ozaki   +13 more
openaire   +2 more sources

First Measurements at Neutron Reflectometers TNR and NERO-2

Poverhnostʹ. Rentgenovskie, sinhrotronnye i nejtronnye issledovaniâ
Paper briefly describes the main units of TNR and NERO-2 neutron reflectometers installed in the hall of horizontal experimental channels of the new high flux PIK-reactor (NRC “Kurchatov Institute”– PNPI) as part of the program for commissioning the first five stations of the instrument base of this reactor.
M. V. Dyachkov   +4 more
openaire   +1 more source

The Impact of Vibration on TNR for a GPR System

2023 IEEE International Symposium on Antennas and Propagation and USNC-URSI Radio Science Meeting (USNC-URSI), 2023
Stephen Pancrazio   +4 more
openaire   +1 more source

TNR to Minimize the Number of Stray Cats/Dogs Population in Indonesia

2021 4th International Conference on Education Technology Management, 2021
Mario Nugroho Willyarto, Carolina Fajar
openaire   +2 more sources

Using Conceptual Mini Games for Learning: The Case of “The Numbers’ Race” (TNR) Application

2012
This study reports the basic characteristics of an experimental conceptual mini-game called “The Numbers’ Race” (TNR), developed with Microsoft Visual Studio. The TNR mini-game concerns a standalone training application that aims at raising achievement levels in the simple mathematical task of addition and giving insights into the strategies used by ...
C. T. Panagiotakopoulos, M. E. Sarris
openaire   +1 more source

Loss of WRN causes instability of expanded CTG trinucleotide repeats (TNRs)

2017
Werner syndrome (WS) is an autosomal and recessive disease. Mutations in the WRN gene causes generation of non-functional WRN protein amounting to genome instability. Patients suffering from WS show accelerated aging, which includes premature graying of hair, loss of subcutaneous fat, atherosclerosis, osteoporosis, diabetes, and an increased incidence ...
openaire   +1 more source

Efficacy of TnR Nasal Mesh for prevention of septal perforation during septoplasty

Auris Nasus Larynx, 2021
Dong Joo Lee   +2 more
exaly  

Home - About - Disclaimer - Privacy