Results 291 to 300 of about 398,460 (354)
GOT1 Inhibition Induces Extracellular Matrix Remodeling in Pancreatic Cancer
Using tumor tissue engineering, we recreated pancreatic cancer and found that inhibiting glutamic‐oxaloacetic transaminase 1 (GOT1) induces extracellular matrix remodeling and secretome rewiring, as well as promotes cell death. ABSTRACT Pancreatic cancer cells rely on glutamine to sustain their survival in the stiff and poorly vascularized tumor ...
Rodrigo Curvello +10 more
wiley +1 more source
ABSTRACT Precise transgene‐free gene upregulation remains a challenge in crop biotechnology, as conventional enhancers often exceed CRISPR‐mediated knock‐in size constraints and face regulatory hurdles. Here we establish a foundational cross‐species resource of compact transcriptional enhancers developed via STEM‐seq, a high‐throughput screening ...
Qi Yao +14 more
wiley +1 more source
Inspired by antifreeze proteins and ion channels in polar fish, β‐cyclodextrin–grafted hyperbranched polyglycerol (CDhPG) mimics interfacial water structuring and ion dehydration. The ice‐matching hydroxyl spacing (2.76 Å) enables IRI activity, while dendritic cavities tailor Zn2+ solvation and enhance low‐temperature conductivity for sustainable ...
Xiaoping Li +10 more
wiley +1 more source
In Parkinson's disease, SHMT1 downregulation disrupts its interaction with PEMT in astrocytes, reducing SAM levels. This leads to H3K4me1 hypomethylation and decreased Slc1a2/Glul expression, ultimately exacerbating neuroexcitotoxicity and dopaminergic neuron loss.
Yue‐Han Chen +17 more
wiley +1 more source
Human islet amyloid polypeptide (hIAPP) was used to mimic T2DM, and Aβ42‐hIAPP co‐oligomers were delivered into the human mature cerebral organoids (COs), which reproduce typical AD pathology and significant neuronal death more closely resembling that of AD patients.
Jin Yan +6 more
wiley +1 more source
4-Aminopyridine reveals presynaptic GABA actions in rat sympathetic ganglia [PDF]
Galvan, Martin +2 more
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Pharmacology & Therapeutics, 1997
The inhibitory glycine receptor (GlyR) is a member of the ligand-gated ion channel receptor superfamily. The GlyR comprises a pentameric complex that forms a chloride-selective transmembrane channel, which is predominantly expressed in the spinal cord and brain stem. We review the pharmacological and physiological properties of the GlyR and relate this
Rajendra, S, Lynch, JW, Schofield, PR
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The inhibitory glycine receptor (GlyR) is a member of the ligand-gated ion channel receptor superfamily. The GlyR comprises a pentameric complex that forms a chloride-selective transmembrane channel, which is predominantly expressed in the spinal cord and brain stem. We review the pharmacological and physiological properties of the GlyR and relate this
Rajendra, S, Lynch, JW, Schofield, PR
openaire +3 more sources
General Pharmacology: The Vascular System, 1978
Abstract 1. Recent studies aimed at elucidating synaptic glycine-receptors have been reviewed. 2. Biochemical and iontophoretic findings have revealed that such receptors exist in several regions of the vertebrate CNS. 3. Subcellular studies with labelled strychnine and glycine have revealed that strychnine does not interact directly with glycine ...
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Abstract 1. Recent studies aimed at elucidating synaptic glycine-receptors have been reviewed. 2. Biochemical and iontophoretic findings have revealed that such receptors exist in several regions of the vertebrate CNS. 3. Subcellular studies with labelled strychnine and glycine have revealed that strychnine does not interact directly with glycine ...
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Glycine Receptor Drug Discovery
2017Postsynaptic glycine receptor (GlyR) chloride channels mediate inhibitory neurotransmission in the spinal cord and brain stem, although presynaptic and extrasynaptic GlyRs are expressed more widely throughout the brain. In humans, GlyRs are assembled as homo- or heteromeric pentamers of α1-3 and β subunits. GlyR malfunctions have been linked to a range
Lynch, Joseph W. +3 more
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The inhibitory neuronal glycine receptor
BioEssays, 1994AbstractGlycine is a major inhibitory neurotransmitter in the spinal cord and in the brain stem, where it acts by activating a chloride conductance. The postsynaptic glycine receptor has been purified and contains two transmembrane subunits of 48 kDa (α) and 58 kDa (β), and a peripheral membrane protein of 93 kDa.
C, Béchade, C, Sur, A, Triller
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