New evidence for secondary axonal degeneration in demyelinating neuropathies

KR Moss, TS Bopp, AE Johnson, A Höke - Neuroscience letters, 2021 - Elsevier
Abstract Development of peripheral nervous system (PNS) myelin involves a coordinated
series of events between growing axons and the Schwann cell (SC) progenitors that will …

[HTML][HTML] Mechanisms and treatments in demyelinating CMT

V Fridman, MA Saporta - Neurotherapeutics, 2021 - Elsevier
Abstract Demyelinating forms of Charcot-Marie-Tooth disease (CMT) are genetically and
phenotypically heterogeneous and result from highly diverse biological mechanisms …

Three‐dimensional genome structure and function

H Liu, H Tsai, M Yang, G Li, Q Bian, G Ding, D Wu… - MedComm, 2023 - Wiley Online Library
Linear DNA undergoes a series of compression and folding events, forming various three‐
dimensional (3D) structural units in mammalian cells, including chromosomal territory …

Genome-edited coincidence and PMP22-HiBiT fusion reporter cell lines enable an artifact-suppressive quantitative high-throughput screening strategy for PMP22 …

NJ Martinez, JC Braisted, PK Dranchak… - ACS Pharmacology & …, 2021 - ACS Publications
Charcot-Marie-Tooth 1A (CMT1A) is the most common form of hereditary peripheral
neuropathies, characterized by genetic duplication of the critical myelin gene Peripheral …

Hereditary neuropathy with liability to pressure palsies misdiagnosed as Guillain–Barré Syndrome: A case report

J Zhu, X Tong, Y Li, G Li, Z Pi - Medicine, 2022 - journals.lww.com
Interventions: The patient was treated with neurotrophic drugs and health education,
including avoiding maintenance of a certain posture for extended periods, which could …

Modulation of Schwann cell homeostasis by the BAP1 deubiquitinase

P Duong, R Ramesh, A Schneider, S Won, AJ Cooper… - Glia, 2023 - Wiley Online Library
Schwann cell programming during myelination involves transcriptional networks that
activate gene expression but also repress genes that are active in neural crest/embryonic …

PLEKHG5-related autosomal recessive lower motor neuron disease with dysmyelination in peripheral nerves

Y Miao, M Yu, L Meng, W Zhang, L He… - Clinical …, 2021 - search.proquest.com
. Discussion This is the third case report of PLEKHG5-related LMND. Because the MNCV
and CMAP amplitude were normal, and EMG showed a neurogenic pattern of muscle de …