Results 261 to 270 of about 122,498 (328)

Boosting BDNF in muscle rescues impaired axonal transport in a mouse model of DI-CMTC peripheral neuropathy. [PDF]

Neurobiol Dis
Rhymes ER, Simkin RL, Qu J, Villarroel-Campos D, Surana S, Tong Y, Shapiro R, Burgess RW, Yang XL, Schiavo G, Sleigh JN.   +10 more
europepmc   +1 more source

Enhanced detection and retrograde axonal transport of PrP^c in peripheral nerve [PDF]

, 2003
Kenneth L. Moya, Raymonde Hässig, Christophe Créminon, Isabelle Laffont, Luigi Di Giamberardino   +4 more
openalex   +1 more source

Materials Selection Principles for Designing Electro‐Thermal Neurons

Advanced Electronic Materials, EarlyView.
Materials property – performance relations are established for new and old electrical materials leveraged as electro‐thermal oscillators emulating neuron dynamics. Robust, reconfigurable, high frequency, low power characteristics are explicitly tied to highly nonlinear electrical transport, small specific heat, and greater electrical than thermal ...
Fatme Jardali, Jenny L. Chong, Yeonju Yu, R. Stanley Williams, Suhas Kumar, Patrick J. Shamberger, Timothy D. Brown   +6 more
wiley   +1 more source

Prominent Axonopathy and Disruption of Axonal Transport in Transgenic Mice Expressing Human Apolipoprotein E4 in Neurons of Brain and Spinal Cord

, 2000
Ina Tesseur, Jo Van Dorpe, Koen Bruynseels, Francisca C. Bronfman, Raf Sciot, Alfons Van Lommel, F. Van Leuven   +6 more
openalex   +1 more source

Vertical Electrolyte‐Gated Transistors: Structures, Materials, Integrations, and Applications

Advanced Electronic Materials, EarlyView.
Vertically structured electrolyte‐gated transistors exhibit significantly improved electrical performance compared to their planar counterparts by decoupling the channel length from the resolutions of the fabrication techniques. Herein, recent progress on the vertical electrolyte‐gated transistors is reviewed from the aspects of device structures ...
Bin Bao, Ting Zhang, Junlei Xie, Jin Wu, Gang He, Lang Jiang, Yanlin Song, Shouguo Wang   +7 more
wiley   +1 more source

Swedish Alzheimer's disease variant perturbs activity of retrograde molecular motors and causes widespread derangement of axonal transport pathways. [PDF]

J Biol Chem
Feole M, Pozo Devoto VM, Dragišić N, Arnaiz C, Bianchelli J, Texlová K, Kovačovicova K, Novotny JS, Havas D, Falzone TL, Stokin GB.   +10 more
europepmc   +1 more source

Enhancing Synaptic Plasticity in Strontium Titanate‐Based Sensory Processing Devices: A Study on Oxygen Vacancy Modulation and Performance in Artificial Neural Networks

Advanced Intelligent Discovery, EarlyView.
This article presents the artificial synapse based on strontium titanate thin films via spin‐coating followed by forming gas annealing to introduce oxygen vacancies. Characterizations (X‐ray photoelectron spectroscopy, electron paramagnetic resonance, Ultraviolet photoelectron spectroscopy (UPS)) confirm increased oxygen vacancies and downward energy ...
Fandi Chen, Zijian Feng, Shuo Zhang, Jie Min, Long Hu, Tianxu Huang, Tingting Mei, Jiyun Kim, Beining Dong, Xinyu Ma, Tao Yin, Jintao Wang, Peiyuan Guan, Tao Wan, Chun‐Ho Lin, Zhi Li, Dewei Chu   +16 more
wiley   +1 more source

Case Report: Hypomyelinating Leukodystrophy Type 20 (HLD20) With Novel CNP Gene Variant

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT This case report describes a child with hypomyelinating leukodystrophy type 20 (HLD20), a rare neurodegenerative disorder characterized by impaired myelin formation. The patient presented with multiple neurodevelopmental abnormalities, including delayed motor milestones, seizures, and abnormal facial features.
Malak Alghamdi, Ghaida Alghamdi, Khalid Hundallah, Dima Jamjoom, Naif Almontashiri, Essa Alharbi, Muhammad Umair, Majid Alfadhel   +7 more
wiley   +1 more source

The role of axonopathy in Parkinson\u27s disease [PDF]

, 2010
O’Malley, Karen L
core   +1 more source

Severe Nerve Enlargement in SOS2‐Related Noonan Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Noonan syndrome is a genetic multisystem congenital disorder, caused by pathogenic variants in genes that encode components of the RAS/MAPK signaling pathway. Pathogenic variants in SOS2 represent less than 2% of cases with NS. The phenotype includes a particularly high prevalence (65%) of lymphatic disease. Recently, severe nerve enlargements
Erika Leenders, Fieke Draaisma, Corrie E. Erasmus, Catelijne Coppens, Lotte E. R. Kleimeier, Melanie Burgers, Tuula Rinne, Martin Zenker, Laura Mazzanti, Wesley Reintjes, Nens van Alfen, Jos M. T. Draaisma   +11 more
wiley   +1 more source