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Calmodulin‐dependent cyclic nucleotide phosphodiesterase activity is altered by 20 μT magnetostatic fields
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1521-186x(200004)21:3<189::aid-bem6>3.0.co;2-lopenalex-snapshot
The effect of static magnetic fields on the rate of calcium/calmodulin-dependent phosphorylation of myosin light chain
inferredcites →https://doi.org/10.1002/bem.2250120202openalex-snapshot
Possible mechanism for the influence of weak magnetic fields on biological systems
inferredcites →https://doi.org/10.1002/bem.2250150306openalex-snapshot
Clarification and application of an ion parametric resonance model for magnetic field interactions with biological systems
inferredcites →https://doi.org/10.1007/978-1-4613-2789-9_1openalex-snapshot
Nonlinear, Nonequilibrium Aspects of Electromagnetic Field Interactions at Cell Membranes
inferredcites →https://doi.org/10.1007/978-1-4615-9837-4_19openalex-snapshot
Extremely Weak AC and DC Magnetic Fields Significantly Affect Myosin Phosphorylation
inferredcites →https://doi.org/10.1007/bf01878387openalex-snapshot
Geomagnetic cyclotron resonance in living cells
inferredcites →https://doi.org/10.1016/s0006-3495(96)79861-2openalex-snapshot
The effects of weak extremely low frequency magnetic fields on calcium/calmodulin interactions
inferredcites →https://doi.org/10.1016/s0021-9258(18)60316-3openalex-snapshot
Adenosine 3‘,5‘-Phosphate in Biological Materials
inferredcites →https://doi.org/10.1016/s0302-4598(96)02226-xopenalex-snapshot
Weak static magnetic field modulation of myosin phosphorylation in a cell-free preparation: Calcium dependence
inferredcites →https://doi.org/10.1146/annurev.ph.55.030193.002235openalex-snapshot
Ca2+ Oscillations in Non-Excitable Cells
inferredcites →https://doi.org/10.3109/15368370009167839openalex-snapshot
Cell Sensitivity to Magnetic Fields
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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“Biological Windows”: A Tribute to W. Ross Adey
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Pulsed electromagnetic field therapy history, state of the art and future
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Electromagnetic field dosimetry for clinical application
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Identification of Unknown Homeopathic Remedies by Delayed Luminescence
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Evidence-Based Use of Pulsed Electromagnetic Field Therapy in Clinical Plastic Surgery
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Exposure of magnetic waves stimulates rapid germination of soybean seeds by enzymatic regulation in cotyledons and embryonic axis
inferred← citeshttps://doi.org/10.1016/j.envres.2021.111505openalex-snapshot
Immunity and electromagnetic fields
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Pulsed Magnetic Field Therapy Increases Tensile Strength in a Rat Achilles’ Tendon Repair Model
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Magnetized water mitigates AlCl3-induced oxidative stress and Alzheimer's-like neurotoxicity in rats
inferred← citeshttps://doi.org/10.1016/j.neulet.2006.11.048openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neuroscience.2014.08.029openalex-snapshot
Neuroprotective effect of weak static magnetic fields in primary neuronal cultures
inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2004.08.008openalex-snapshot
Effects of static magnetic fields at the cellular level
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Pulsed magnetic field: A contemporary approach offers to enhance plant growth and yield of soybean
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Electromagnetic effects – From cell biology to medicine
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The rhizosphere soil properties and bacteria community of poplar are affected by magnetic field under salt condition
inferred← citeshttps://doi.org/10.1016/j.snb.2020.128444openalex-snapshot
3D cell capture and sensing array electrode (3D ECCSA) under extremely low frequency electromagnetic fields (ELF-EMF)
inferred← citeshttps://doi.org/10.1080/09553000400029502openalex-snapshot
Extremely low frequency (ELF) magnetic fields and apoptosis: a review
inferred← citeshttps://doi.org/10.1080/09593330.2014.952341openalex-snapshot
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Magnetic Field Therapy: A Review
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Expanding Use of Pulsed Electromagnetic Field Therapies
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4 Hz Magnetic Field Decreases Oxidative Stress in Mouse Brain: A Chemiluminescence Study
inferred← citeshttps://doi.org/10.1081/jbc-200026319openalex-snapshot
Myosin Light Chain Phosphorylation Modification Depending on Magnetic Fields. I. Theoretical
inferred← citeshttps://doi.org/10.1081/jbc-200040313openalex-snapshot
Myosin Light Chain Modification Depending on Magnetic Fields: II. Experimental
inferred← citeshttps://doi.org/10.1109/iciafs.2010.5715697openalex-snapshot
Analysis of biological effects and limits of exposure to weak magnetic fields
inferred← citeshttps://doi.org/10.1109/tmag.2004.830202openalex-snapshot
Effects of Static Magnetic Fields on Early Embryonic Development of the Sea Urchin Echinometra mathaei
inferred← citeshttps://doi.org/10.1111/j.1526-4637.2007.00324.xopenalex-snapshot
A Randomized Controlled Trial of the Effects of a Combination of Static and Dynamic Magnetic Fields on Carpal Tunnel Syndrome
inferred← citeshttps://doi.org/10.1159/000324003openalex-snapshot
Effects of Acute and Chronic Low Frequency Electromagnetic Field Exposure on PC12 Cells during Neuronal Differentiation
inferred← citeshttps://doi.org/10.1159/000398803openalex-snapshot
Microwave-Induced Structural and Functional Injury of Hippocampal and PC12 Cells Is Accompanied by Abnormal Changes in the NMDAR-PSD95-CaMKII Pathway
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Mechanisms and therapeutic applications of electromagnetic therapy in Parkinson’s disease
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Magnetoreception in microorganisms and fungi
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Effect of Magnetic Field and UV-C Radiation on Postharvest Fruit Properties
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Effect of alternating the magnetic feld on phosphate metabolism in the nervous system of Helix pomatia
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Extremely low frequency magnetic fields induce oxidative stress in rat brain
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Effect of the magnetized water supplementation on blood glucose, lymphocyte DNA damage, antioxidant status, and lipid profiles in STZ-induced rats
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Four months of magnetized water supplementation improves glycemic control, antioxidant status, and cellualr DNA damage in db/db mice
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Effect of the Magnetized Water Supplementation on Lymphocyte DNA Damage in Mice Treated with Diethylnitrosamine
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