Nanoparticle mind control (framework)?

Yes, nanoparticles themselves do not control the mind, they can only connect to the thought. Then it would be possible to "pull out" any memory, idea, feeling, thought into any computer. And vice versa, from any computer it would be possible to "upload" to the creature and suggest anything to it...
The human body is made up of several bodies and although AI can work on the astral plane, the mind with the soul is unprocessable in this way, if the individual uses intuition and has a conscience.
The problem occurs in an instant with beings that do not have a soul or beings that have gone through a successful MK Ultra reprogramming where there was a split personality - in this way, they become controllable robots in a human (and animal) body. Sometimes against will being.
Nanotechnology has been used in secret military programs in this way a very long time ago.

I hear you.

Exactly.
In addition, any crystal can scan and send at the same time. And what is a monitor or a screen made of...?!...
Also the jewelry that people wear -transmitters, amplifiers..

They hear you.

Interesting! "They". being evil ones, or Benevolent ones?

High and intense noises can have a severe impact on people living with Autism. Autistic children are very sensitive to specific sounds and pitches that others are not affected by. The downside to sound sensitivity is that noise quickly becomes painful and can even trigger a panic attack.

Acoustic attenuation is a measure of the energy loss of sound propagation in media. Most media have viscosity and are therefore not ideal media. When sound propagates in such media, there is always thermal consumption of energy caused by viscosity.

An attenuated vaccine (or a live attenuated vaccine, LAV) is a vaccine created by reducing the virulence of a pathogen, but still keeping it viable (or "live").

2: Helical motion of a charged particle around a magnetic field line

When a charged particle enters in a magnetic field at an angle other than 90
o
then a component of velocity takes it under linear motion and other component , under circular motion ,and the combined effect is a helical motion .

Ion involvement:
SCN2A is the not the only sodium channel linked to autism. Children with mutations in SCN1A, a sodium channel that works in neurons that dampen brain activity, have a severe form of epilepsy called Dravet syndrome and, sometimes, autism.

Light-gated ion channels are a group of transmembrane proteins that form ion channels; pores which open or close in response to light.

As an emerging biomedical imaging technology, photoacoustic (PA) imaging, also named as optoacoustic imaging, has been rapidly developed in the past decades and extensively explored for potential applications in preclinical and clinical settings1,2,3,4,5. By illuminating a biological sample with nanosecond pulsed light and then detecting the light-generated ultrasound (US) signal as a result of thermoelastic expansion, a 2D or 3D map reflecting the optical-absorption contrast in the sample can be produced via different image reconstruction methods. By combining the merits of both light and ultrasound, PA imaging is capable of presenting highly-sensitive optical spectroscopic contrast in subsurface biological tissue at high ultrasonic spatial resolution.

Deep brain stimulation via implanted electrodes can alleviate neuronal disorders. However, its applicability is constrained by side effects resulting from the insertion of electrodes into the brain. Here, we show that systemically administered piezoelectric nanoparticles producing nitric oxide and generating direct current under high-intensity focused ultrasound can be used to stimulate deep tissue in the brain. The release of nitric oxide temporarily disrupted tight junctions in the blood–brain barrier, allowing for the accumulation of the nanoparticles into brain parenchyma, and the piezoelectrically induced output current stimulated the release of dopamine by dopaminergic neuron-like cells. In a mouse model of Parkinson’s disease, the ultrasound-responsive nanoparticles alleviated the symptoms of the disease without causing overt toxicity. The strategy may inspire the development of other minimally invasive therapies for neurodegenerative diseases.

Acquired hearing loss occurs after birth. Common viruses that can cause acquired hearing loss include measles, Varicella-Zoster Virus (the virus that causes Chicken Pox and Shingles), and the mumps.

MMR=measles, mumps, and rubella combination vaccine. MMRV = measles, mumps, rubella, and varicella combination vaccine. Measles=Rubeola. Measles = ”10-day,” “hard” and “red” measles. Rubella = also called “German” or “3-day” measles.

One of the more alarming complications of mumps is hearing loss. We still don't know exactly how mumps causes damage to hearing. Some experts think it may damage the cochlea, the snail-shaped structure in your ear that house stereocilia and the stria vascularis. Stereocilia, otherwise known as hair cells, translate sound vibrations into nerve impulses for the brain to interpret as sound.

nerve impulse
/ˈnəːv ˌɪmpʌls/

plural noun: nerve impulses
a signal transmitted along a nerve fibre. It consists of a wave of electrical depolarization that reverses the potential difference across the nerve cell membranes.

In biology, depolarization or hypopolarization is a change within a cell, during which the cell undergoes a shift in electric charge distribution, resulting in less negative charge inside the cell compared to the outside.

The depolarization is brought about by the entry of sodium and calcium ions that results from the opening of membrane channels.

Genetic analysis of ASD has advanced dramatically through genome sequencing, which has identified >500 genes with mutations in ASD. Mutations in the voltage sensor of the voltage-gated potassium (KV) channel KV7 are frequently associated with ASD. We discovered that these ASD mutations cause an ionic leak through the voltage sensor, termed gating pore current. When these mutations were inserted into the genome of mouse dopamine neurons, they caused a dramatic alteration in the ability of those neurons to fire action potentials in response to electrical stimulation. These changes would impair information processing in neurons, leading to broad changes in brain function.

Gating currents are generated by the movement of specific charges in the transmembrane helices of V(oltage)-gated ion channel proteins.

Synthetic ion channels are de novo chemical compounds that insert into lipid bilayers, form pores, and allow ions to flow from one side to the other.[1] They are man-made analogues of natural ion channels, and are thus also known as artificial ion channels. Compared to biological channels, they usually allow fluxes of similar magnitude but are

minuscule in size (less than 5k Dalton vs. > 100k Dalton),
diverse in molecular architecture, and
may rely on diverse supramolecular interactions to pre-form the active, conducting structures.[2][3][4][5]

Coronaviruses are spherical particles with diameter of ~125 nm enclosed in an envelope bilayer, in which the membrane (M), envelope (E) and spike (S) structural proteins are embedded (3). The S protein generates the surface spikes that mediate receptor binding and membrane fusion between the virus and the host cell, while the E and M proteins maintain the envelope shape (4). Inside the viral envelope, nucleocapsid (N) proteins stabilize the single-stranded RNA genome (4).

Many studies have established the relevance of the E protein and protein 3a as fundamental pro-inflammatory SARS-CoV virulence factors (5–8), and additional studies have suggested that the inflammatory properties of E and 3a are related to their induction of ion conductances in membranes, i.e. that they are ion channel proteins (9–12). Since the initial characterization of influenza M2 (13), viral proteins which form ion channels themselves (viroporins) (14), or which can modulate host cell ion channel function (e.g. HIV-1 Vpu) (15, 16), have been reported in a variety of virus species (17), and repeatedly proposed as potential anti-viral drug targets (17–19).

"studies have suggested that the inflammatory properties of E and 3a are related to their induction of ion conductances in membranes, i.e. that they are ion channel proteins (9–12)"

Ions move across the cell membrane through specific ion channels. When these channels open, the permeability and electrical conductance to their respective ions increases, which leads to a change in the membrane potential.

These results indicate the abnormalities in mitochondrial respiratory control linking mitochondrial function with autism.

The mitochondrial membrane potential (ΔΨm) generated by proton pumps (Complexes I, III and IV) is an essential component in the process of energy storage during oxidative phosphorylation. Together with the proton gradient (ΔpH), ΔΨm forms the transmembrane potential of hydrogen ions which is harnessed to make ATP.

Oxidative phosphorylation is the process where energy is harnessed through a series of protein complexes embedded in the inner-membrane of mitochondria (called the electron transport chain and ATP synthase) to create ATP.

An electron transport chain is a series of protein complexes and other molecules that transfer electrons from electron donors to electron acceptors via redox reactions and couples this electron transfer with the transfer of protons across a membrane.

Förster, or fluorescence, resonance energy transfer (FRET) provides fluorescence signals sensitive to intra- and inter-molecular distances in the 1 to 10 nm range. Widely applied in the fluorescence imaging environment, FRET enables visualization of physicochemical processes in molecular interactions and conformations. In this paper, we report photoacoustic imaging of FRET, based on nonradiative decay that produces heat and subsequent acoustic waves. Estimates of the energy transfer efficiency by photoacoustic microscopy were compared to those obtained by fluorescence confocal microscopy. The experimental results in tissue phantoms show that photoacoustic microscopy is capable of FRET imaging with an enhanced penetration depth. Through its ability to three-dimensionally image tissue with scalable resolution, photoacoustic microscopy could be a beneficial biomedical tool to broaden the in vivo application of FRET.

FRET is the radiationless transmission of energy from a donor molecule to an acceptor molecule. The donor molecule is the dye or chromophore that initially absorbs the energy and the acceptor is the chromophore to which the energy is subsequently transferred.

https://jnnp.bmj.com/conte...

Obstacles of targeted inner ear delivery include anatomic inaccessibility, biotherapeutic instability, and nonspecific delivery. Advances in nanotechnology may provide a solution to these barriers. Nanoparticles can stabilize and carry biomaterials across the round window membrane into the inner ear, and ligand bioconjugation onto nanoparticle surfaces allows for specific targeting.

Implantable middle ear hearing devices (IMEHDs) have been developed as a new technology to overcome the limitations of conventional hearing aids. The piezoelectric cantilever transducers currently used in the IMEHDs have the advantages of low power consumption and ease of fabrication, but generate less high-frequency output. To address this problem, we proposed and designed a new piezoelectric transducer based on a piezoelectric stack for the IMEHD. This new transducer, attached to the incus body with a coupling rod, stimulates the ossicular chain in response to the expansion-and-contraction of its piezoelectric stack. To test its feasibility for hearing loss compensation, a bench testing of the transducer prototype and a temporal bone experiment were conducted, respectively.

Bench testing results showed that the new transducer did have a broad frequency bandwidth. Besides, the transducer was found to have a low total harmonic distortion (

The luminescence of semiconductor quantum dots (QDs) can be adjusted using the piezotronic effect. An external mechanical force applied on the QD generates a piezoelectric potential, which alters the luminescence of the QD.

The rationale behind our approach is very simple. In many retinal diseases, cellular degeneration and vision loss involve dysfunction or death of photoreceptors and/or associated neurons in the visual pathway – but you can inhibit this process, and maintain functionality, by directly triggering activity in visual pathway neurons. We achieve this via intravitreal injection of quantum dots. It’s an entirely new approach to the retinal implant concept, and it is potentially applicable to any condition associated with retinal degeneration. So how does it work? Briefly, it’s a sophisticated take on an idea that’s been around well before Mary Shelley wrote Frankenstein – namely, electrical stimulation of neural responses.

Prior to the use of quantum dots, the electrical innovation approach relied on invasive, retinal implants: for example, the Second Sight “Argus” device. But these types of retinal prostheses have some fundamental drawbacks: the invasive nature of the implantation procedure limits their use to patients who have lost almost all vision, and the nature of the device is such that it presents the brain with a stimulus that the visual system must learn to interpret. Our approach, by contrast, involves the application of a suspension of quantum dots. The size and construction of these particles are such that they easily diffuse into and across the retina, assisted by the natural processes of the eye which move the vitreous through the retina. In effect, we are using the vitreous as a reservoir to supply quantum dots to visual neurons.

Quantum effect

The quantum dot mechanism of action is strikingly simple. While in the retina, the nanoparticles are stimulated by visible light entering the eye – and if a quantum dot is stimulated while it is in close proximity to a neural cell, it triggers an action potential in that cell which is interpreted as vision by the brain.

Piezoelectricity (/ˌpiːzoʊ-, ˌpiːtsoʊ-, paɪˌiːzoʊ-/, US: /piˌeɪzoʊ-, piˌeɪtsoʊ-/)[1] is the electric charge that accumulates in certain solid materials—such as crystals, certain ceramics, and biological matter such as bone, DNA, and various proteins—in response to applied mechanical stress.[2] The word piezoelectricity means electricity resulting from pressure and latent heat. It is derived from the Greek word πιέζειν; piezein, which means to squeeze or press, and ἤλεκτρον ēlektron, which means amber, an ancient source of electric charge

"Piezoelectricity (/ˌpiːzoʊ-, ˌpiːtsoʊ-, paɪˌiːzoʊ-/, US: /piˌeɪzoʊ-, piˌeɪtsoʊ-/)[1] is the electric charge that accumulates in certain solid materials—such as crystals"

TMV was the first virus to be discovered. Although it was known from the late 19th century that a non-bacterial infectious disease was damaging tobacco crops, it was not until 1930 that the infectious agent was determined to be a virus. It is the first pathogen identified as a virus. The virus was crystallised by W.M. Stanley.