Results 91 to 100 of about 6,650,662 (298)

S.M. Simpson Ltd. -- bulk bins

open access: yes, 1960
Possibly at Rutland Field. S.M. Simpson Ltd.

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Augmenting and Assaying Nav1.1 Protein Quantity for Dravet Syndrome Therapy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Dravet Syndrome (DS) is a developmental and epileptic encephalopathy predominantly caused by heterozygous loss‐of‐function variants in SCN1A, which encodes Nav1.1. Conserved upstream open reading frames (uORFs) in SCN1A were validated to regulate translation in reporter assays, demonstrating the therapeutic viability of increasing Nav1.1 from ...
Aiswarya Saravanan   +7 more
wiley   +1 more source

Potential Role of Synaptic Activity to Inhibit LTD Induction in Rat Visual Cortex

open access: yesNeural Plasticity, 2016
Long-term depression (LTD), a widely studied form of activity-dependent synaptic plasticity, is typically induced by prolonged low-frequency stimulation (LFS).
Matthew R. Stewart, Hans C. Dringenberg
doaj   +1 more source

S.M. Simpson Ltd. -- gang saw

open access: yes, 1949
Two workers in S.M. Simpson Ltd.

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The Comprehensive Live Cell‐Based Cytotoxicity Assay for Monitoring Disease Activity and Guiding Rescue Therapy in Acute Attacks of NMOSD

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Neuromyelitis optica spectrum disorder (NMOSD) is a devastating neurological disease that lacks serological biomarkers that can accurately reflect disease activity. We established a live cell‐based assay (LCBA) using serum with endogenous complement to quantify the overall cytotoxicity, offering a novel functional tool for monitoring
Xiaona Xu   +10 more
wiley   +1 more source

S.M. Simpson Ltd. -- machine shop

open access: yes, 1955
The saw sharpening room was in the machine shop at the S.M. Simpson Ltd.

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Stage‐Specific Patterns of Imaging and Non‐Motor Biomarkers in Spinocerebellar Ataxia Type 3

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Advancements in disease‐modifying therapies for spinocerebellar ataxia Type 3 (SCA3) underscore the need for robust biomarkers to monitor disease progression and evaluate treatment efficacy. Although motor phenotypes have been well characterized, less is known about non‐motor and imaging‐based features across different disease stages.
Chun Li   +17 more
wiley   +1 more source

Synaptopodin is required for long-term depression at Schaffer collateral-CA1 synapses

open access: yesMolecular Brain
Synaptopodin (SP), an actin-associated protein found in telencephalic neurons, affects activity-dependant synaptic plasticity and dynamic changes of dendritic spines.
Yanis Inglebert   +4 more
doaj   +1 more source

S.M. Simpson Ltd. -- lumberyard, winter

open access: yes, 1948
Snow-covered lumberyard outside of S.M. Simpson Ltd. sawmill.

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