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Monthly Archives: July 2015
Human Genetics
Posted: July 31, 2015 at 8:44 am
POST
It has been a long time since Human Genetics got introduced to mankind. One can definitely think of it as a great achievement in the entire history of humans. It is the alteration of genes in a human being for making him or her resistant to different kind of diseases that can prove deadly, because Read more
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Major area for human genetic engineering debate revolves around the ethics involved in testing of genetics. Other areas for debate include selective eugenics as well as genetic discrimination. Apart from the above debates, the scientists have now been found busy on making debates on some other frightening prospects of human genetic engineering. Human genetic engineering Read more
POST
Human genetics research is a revolutionary change in the field of medical science. It has made several advances in this field. It entered this field many years ago when Hippocrates discovered nature laws can easily describe the body workings. This revolution identified that contaminated water is a primary reason that leads to a disease like Read more
POST
Many human genetic engineering pros and cons are there that have stayed the same since its introduction to humanity. When the humans started harnessing the atomic powers, then just few years later they also start recognizing the effects of human genetic engineering on mankind. Many scientists have a belief that gene therapy can be a Read more
POST
A primary debate topic among the people from western civilization is the effects of human cloning and genetic engineering. This topic has given place to a lot of controversies in that civilization. It is an asexual reproduction using genetic engineering. There is a huge relation between human cloning and genetic engineering. In fact, cloning cannot Read more
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Human Genetic Engineering Pros And Cons
Posted: at 8:44 am
Human Genetic Engineering Pros And Cons 3.78/5 (75.54%) 1970 votes
Many human genetic engineering pros and cons are there that have stayed the same since its introduction to humanity. When the humans started harnessing the atomic powers, then just few years later they also start recognizing the effects of human genetic engineering on mankind. Many scientists have a belief that gene therapy can be a mainstream for saving lives of many people. A lot of human genetic engineering pros and cons have been involved since the evolution of genetic engineering. Mentioned below are some important advantages or pros of genetic engineering:
Other human genetic engineering pros and cons include the desirable characteristics in different plants and animals at the same time convenient. One can also do the manipulation of genes in trees or big plants. This will enable the trees to absorb increased amount of carbon dioxide, and it will reduce the effects of global warming. However, there is a question from critics that whether man has the right to do such manipulations or alterations in the genes of natural things.
With human genetic engineering, there is always a chance for altering the wheat plants genetics, which will then enable it to grow insulin. Human genetic engineering pros and cons have been among the concern of a lot of people involved in genetic engineering. Likewise the pros, certain cons are there of using the genetic engineering. Mentioned below are the cons of human genetic engineering:
The evolution of genetic engineering gets the consideration of being the biggest breakthroughs in the history of mankind after the evolution of atomic energy, and few other scientific discoveries. However, human genetic engineering pros and cons together have contributed a lot in creating a controversial image of it among the people.
All these eventualities have forced the government of many countries to make strict legislation laws to put restrictions on different experiment being made on human genetic engineering. They have made this decision by considering different human genetic engineering pros and cons.
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TorBrowser – anonymity & circumvention | security in-a-box
Posted: July 30, 2015 at 4:43 pm
If you live in an area where accessing the Tor Network directly, as described above, is not possible or risky, you can configure Tor to try and circumvent the obstacles that are in place.
Step 1: Navigate to the Tor Browser folder, and then double click to activate the following screen:
Figure 4: The Tor Network Settings panel
Step 2: Click the button which will open a new window. You will be asked three short configuration questions to help you access the Tor Network.
Question 1: Proxy Access; If you need to access the Internet via a proxy check yes and then press . If you do not use a proxy check no and then press .
If you selected yes above, fill in your proxy settings on the following screen. If you do not know your proxy settings, check your regular browser settings. In Firefox you can find them in Options > Advanced > Network tab in Connection Settings section. In other browsers you may look for Internet Options. Use the Help feature within your browser for further assistance.
Figure 5: Proxy settings screen
Question 2: Restricted Ports; If you are accessing the Internet through a firewall that only allows access over certain ports, for example port 80 or 443 for web browsing, select yes and press to configure the ports, otherwise select no and press .
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TorBrowser - anonymity & circumvention | security in-a-box
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Mars – Wikipedia, the free encyclopedia
Posted: at 4:42 pm
Mars is the fourth planet from the Sun and the second smallest planet in the Solar System, after Mercury. Named after the Roman god of war, it is often referred to as the "Red Planet" because the iron oxide prevalent on its surface gives it a reddish appearance.[15] Mars is a terrestrial planet with a thin atmosphere, having surface features reminiscent both of the impact craters of the Moon and the volcanoes, valleys, deserts, and polar ice caps of Earth. The rotational period and seasonal cycles of Mars are likewise similar to those of Earth, as is the tilt that produces the seasons. Mars is the site of Olympus Mons, the largest volcano and second-highest known mountain in the Solar System, and of Valles Marineris, one of the largest canyons in the Solar System. The smooth Borealis basin in the northern hemisphere covers 40% of the planet and may be a giant impact feature.[16][17] Mars has two moons, Phobos and Deimos, which are small and irregularly shaped. These may be captured asteroids,[18][19] similar to 5261 Eureka, a Mars trojan.
Until the first successful Mars flyby in 1965 by Mariner 4, many speculated about the presence of liquid water on the planet's surface. This was based on observed periodic variations in light and dark patches, particularly in the polar latitudes, which appeared to be seas and continents; long, dark striations were interpreted by some as irrigation channels for liquid water. These straight line features were later explained as optical illusions, though geological evidence gathered by unmanned missions suggests that Mars once had large-scale water coverage on its surface at some earlier stage of its life.[20] In 2005, radar data revealed the presence of large quantities of water ice at the poles[21] and at mid-latitudes.[22][23] The Mars rover Spirit sampled chemical compounds containing water molecules in March 2007. The Phoenix lander directly sampled water ice in shallow Martian soil on July 31, 2008.[24]
Mars is host to seven functioning spacecraft: five in orbit2001 Mars Odyssey, Mars Express, Mars Reconnaissance Orbiter, MAVEN and Mars Orbiter Missionand two on the surfaceMars Exploration Rover Opportunity and the Mars Science Laboratory Curiosity. Defunct spacecraft on the surface include MER-A Spirit and several other inert landers and rovers such as the Phoenix lander, which completed its mission in 2008. Observations by the Mars Reconnaissance Orbiter have revealed possible flowing water during the warmest months on Mars.[25] In 2013, NASA's Curiosity rover discovered that Mars's soil contains between 1.5% and 3% water by mass (about two pints of water per cubic foot or 33 liters per cubic meter, albeit attached to other compounds and thus not freely accessible).[26]
Mars can easily be seen from Earth with the naked eye, as can its reddish coloring. Its apparent magnitude reaches 2.91,[6] which is surpassed only by Jupiter, Venus, the Moon, and the Sun. Optical ground-based telescopes are typically limited to resolving features about 300 kilometers (190mi) across when Earth and Mars are closest because of Earth's atmosphere.[27]
Animation (00:40) showing major features
Mars is approximately half the diameter of Earth, and its surface area is only slightly less than the total area of Earth's dry land.[6] Mars is less dense than Earth, having about 15% of Earth's volume and 11% of Earth's mass. Although Mars is larger and more massive than Mercury, Mercury has a higher density. This results in the two planets having a nearly identical gravitational pull at the surfacethat of Mars is stronger by less than 1%. The red-orange appearance of the Martian surface is caused by iron(III) oxide, more commonly known as hematite, or rust.[28] It can also look like butterscotch,[29] and other common surface colors include golden, brown, tan, and greenish, depending on the minerals present.[29]
Like Earth, Mars has differentiated into a dense metallic core overlaid by less dense materials.[30] Current models of its interior imply a core region about 1,79465 kilometers (1,11540mi) in radius, consisting primarily of iron and nickel with about 1617% sulfur.[31] This iron(II) sulfide core is thought to be twice as rich in lighter elements than Earth's core.[32] The core is surrounded by a silicate mantle that formed many of the tectonic and volcanic features on the planet, but it now appears to be dormant. Besides silicon and oxygen, the most abundant elements in the Martian crust are iron, magnesium, aluminum, calcium, and potassium. The average thickness of the planet's crust is about 50km (31mi), with a maximum thickness of 125km (78mi).[32] Earth's crust, averaging 40km (25mi), is only one third as thick as Mars's crust, relative to the sizes of the two planets. The InSight lander planned for 2016 will use a seismometer to better constrain the models of the interior.[33]
Mars is a terrestrial planet that consists of minerals containing silicon and oxygen, metals, and other elements that typically make up rock. The surface of Mars is primarily composed of tholeiitic basalt,[34] although parts are more silica-rich than typical basalt and may be similar to andesitic rocks on Earth or silica glass. Regions of low albedo show concentrations of plagioclase feldspar, with northern low albedo regions displaying higher than normal concentrations of sheet silicates and high-silicon glass. Parts of the southern highlands include detectable amounts of high-calcium pyroxenes. Localized concentrations of hematite and olivine have also been found.[35] Much of the surface is deeply covered by finely grained iron(III) oxide dust.[36][37]
Although Mars has no evidence of a current structured global magnetic field,[41] observations show that parts of the planet's crust have been magnetized, and that alternating polarity reversals of its dipole field have occurred in the past. This paleomagnetism of magnetically susceptible minerals has properties that are similar to the alternating bands found on the ocean floors of Earth. One theory, published in 1999 and re-examined in October 2005 (with the help of the Mars Global Surveyor), is that these bands demonstrate plate tectonics on Mars four billion years ago, before the planetary dynamo ceased to function and the planet's magnetic field faded away.[42]
During the Solar System's formation, Mars was created as the result of a stochastic process of run-away accretion out of the protoplanetary disk that orbited the Sun. Mars has many distinctive chemical features caused by its position in the Solar System. Elements with comparatively low boiling points, such as chlorine, phosphorus, and sulphur, are much more common on Mars than Earth; these elements were probably removed from areas closer to the Sun by the young star's energetic solar wind.[43]
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Transhumanism race against humanity theme in "Hybrid World …
Posted: July 29, 2015 at 1:42 pm
"Hybrid World: The Plan to Modify and Control the Human Race" movie review
Hybrid World directed by Ken Klein, produced by Warren Croyle
Waking Times' recent article on "Transhumanism -- The Wholesale Design of Humanity" opened up a whole new biotechnology and technological confluence which this Examiner didn't know about.
Transhumanists envision the wholesale redesign of humanity, and its movement (H+) has steadily and stealthily been gathering force over the past two decades.
Transhumanism will change the world by eliminating sickness and famine, while critics believe that transforming mankind is an affront to morality and human dignity.
Transhumanism is the term coined by academics, researchers, pharmacologists, industrialists, military strategists, and physicists in the new frontier of altering the human body, robotization, enmeshing man in metal, or interfacing them with artificial intelligence. It involves more than just transgenics or genetic manipulation. All options are on the table for tinkering with humans via nanobots, artificial implants, dietary changes--even cognitive programming.
According to Zoltan Istvan, 2016 US Presidential candidate for the Transhumanist Party:
With billionaires like Peter Thiel and Larry Ellison openly putting money into aging research, and behemoths like Google recently forming its anti-aging company Calico, there's real confidence that the human race may end up stopping death in the next few decades.
Professor Yuval Noah Harari claims in a new book interview with the Telegraph:
I think it is likely in the next 200 years or so homo sapiens will upgrade themselves into some idea of a divine being, either through biological manipulation or genetic engineering of by the creation of cyborgs, part organic part non-organic.
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Gene therapy – Wikipedia, the free encyclopedia
Posted: July 28, 2015 at 9:57 pm
Gene therapy is the therapeutic delivery of nucleic acid polymers into a patient's cells as a drug to treat disease. Gene therapy could be a way to fix a genetic problem at its source. The polymers are either expressed as proteins, interfere with protein expression, or possibly correct genetic mutations.
The most common form uses DNA that encodes a functional, therapeutic gene to replace a mutated gene. The polymer molecule is packaged within a "vector", which carries the molecule inside cells.
Gene therapy was conceptualized in 1972, by authors who urged caution before commencing human gene therapy studies. The first gene therapy experiment approved by the US Food and Drug Administration (FDA) occurred in 1990, when Ashanti DeSilva was treated for ADA-SCID.[1] By January 2014, some 2,000 clinical trials had been conducted or approved.[2]
Early clinical failures led to dismissals of gene therapy. Clinical successes since 2006 regained researchers' attention, although as of 2014, it was still largely an experimental technique.[3] These include treatment of retinal disease Leber's congenital amaurosis,[4][5][6][7]X-linked SCID,[8] ADA-SCID,[9][10]adrenoleukodystrophy,[11]chronic lymphocytic leukemia (CLL),[12]acute lymphocytic leukemia (ALL),[13]multiple myeloma,[14]haemophilia[10] and Parkinson's disease.[15] Between 2013 and April 2014, US companies invested over $600 million in the field.[16]
The first commercial gene therapy, Gendicine, was approved in China in 2003 for the treatment of certain cancers.[17] In 2012 Glybera, a treatment for a rare inherited disorder, became the first treatment to be approved for clinical use in either Europe or the United States after its endorsement by the European Commission.[3][18]
Following early advances in genetic engineering of bacteria, cells and small animals, scientists started considering how to apply it to medicine. Two main approaches were considered replacing or disrupting defective genes.[19] Scientists focused on diseases caused by single-gene defects, such as cystic fibrosis, haemophilia, muscular dystrophy, thalassemia and sickle cell anemia. Glybera treats one such disease, caused by a defect in lipoprotein lipase.[18]
DNA must be administered, reach the damaged cells, enter the cell and express/disrupt a protein.[20] Multiple delivery techniques have been explored. The initial approach incorporated DNA into an engineered virus to deliver the DNA into a chromosome.[21][22]Naked DNA approaches have also been explored, especially in the context of vaccine development.[23]
Generally, efforts focused on administering a gene that causes a needed protein to be expressed. More recently, increased understanding of nuclease function has led to more direct DNA editing, using techniques such as zinc finger nucleases and CRISPR. The vector incorporates genes into chromosomes. The expressed nucleases then "edit" the chromosome. As of 2014 these approaches involve removing cells from patients, editing a chromosome and returning the transformed cells to patients.[24]
Other technologies employ antisense, small interfering RNA and other DNA. To the extent that these technologies do not alter DNA, but instead directly interact with molecules such as RNA, they are not considered "gene therapy" per se.[citation needed]
Gene therapy may be classified into two types:
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Human Genetic Engineering – Popular Issues
Posted: at 9:57 pm
Human Genetic Engineering - A Hot Issue! Human genetic engineering is a hot topic in the legislative and executive branches of the U.S. government. Time will tell how committed the United States will be regarding the absolute ban on human cloning.
Human Genetic Engineering - Position of the U.S. Government Human genetic engineering has made its way to Capitol Hill. On July 31, 2001, the House of Representatives passed a bill which would ban human cloning, not only for reproduction, but for medical research purposes as well. The Human Cloning Prohibition Act of 2001, sponsored by Rep. Weldon (R-fL) and co-sponsored by over 100 Representatives, passed by a bipartisan vote of 265-to-162. The Act makes it unlawful to: "1) perform or attempt to perform human cloning, 2) participate in an attempt to perform cloning, or 3) ship or receive the product of human cloning for any purpose." The Act also imposes penalties of up to 10 years imprisonment and no less than $1,000,000 for breaking the law. The same bill, sponsored by Sen. Brownback (R-kS), is currently being debated in the Senate.
The White House also opposes "any and all attempts to clone a human being; [they] oppose the use of human somatic cell nuclear transfer cloning techniques either to assist human reproduction or to develop cell or tissue-based therapies."
Human Genetic Engineering - The Problems There are many arguments against human genetic engineering, including the established safety issues, the loss of identity and individuality, and human diversity. With therapeutic cloning, not only do the above issues apply, but you add all the moral and religious issues related to the willful killing of human embryos. Maybe the greatest concern of all is that man would become simply another man-made thing. As with any other man-made thing, the designer "stands above [its design], not as an equal but as a superior, transcending it by his will and creative prowess." The cloned child will be dehumanized. (See, Leon Kass, Preventing a Brave New World: Why we should ban human cloning now, New Republic Online, May 21, 2001.)
Human Genetic Engineering - A Final Thought Human genetic engineering leads to man usurping God as the almighty creator and designer of life. No longer will a child be considered a blessing from God, but rather, a product manufactured by a scientist. Man will be a created being of man. However, man was always intended to be a created being of God, in His absolute love, wisdom and glory.
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Human Genetics Alert – The Threat of Human Genetic Engineering
Posted: at 9:57 pm
David King
The main debate around human genetics currently centres on the ethics of genetic testing, and possibilities for genetic discrimination and selective eugenics. But while ethicists and the media constantly re-hash these issues, a small group of scientists and publicists are working towards an even more frightening prospect: the intentional genetic engineering of human beings. Just as Ian Wilmut presented us with the first clone of an adult mammal, Dolly, as a fait accompli, so these scientists aim to set in place the tools of a new techno-eugenics, before the public has ever had a chance to decide whether this is the direction we want to go in. The publicists, meanwhile are trying to convince us that these developments are inevitable. The Campaign Against Human Genetic Engineering, has been set up in response to this threat.
Currently, genetic engineering is only applied to non-reproductive cells (this is known as 'gene therapy') in order to treat diseases in a single patient, rather than in all their descendants. Gene therapy is still very unsuccessful, and we are often told that the prospect of reproductive genetic engineering is remote. In fact, the basic technologies for human genetic engineering (HGE) have been available for some time and at present are being refined and improved in a number of ways. We should not make the same mistake that was made with cloning, and assume that the issue is one for the far future.
In the first instance, the likely justifications of HGE will be medical. One major step towards reproductive genetic engineering is the proposal by US gene therapy pioneer, French Anderson, to begin doing gene therapy on foetuses, to treat certain genetic diseases. Although not directly targeted at reproductive cells, Anderson's proposed technique poses a relatively high risk that genes will be 'inadvertently' altered in the reproductive cells of the foetus, as well as in the blood cells which he wants to fix. Thus, if he is allowed to go ahead, the descendants of the foetus will be genetically engineered in every cell of their body. Another scientist, James Grifo of New York University is transferring cell nuclei from the eggs of older to younger women, using similar techniques to those used in cloning. He aims to overcome certain fertility problems, but the result would be babies with three genetic parents, arguably a form of HGE. In addition to the two normal parents, these babies will have mitochondria (gene-containing subcellular bodies which control energy production in cells) from the younger woman.
Anderson is a declared advocate of HGE for medical purposes, and was a speaker at a symposium last year at UCLA, at which advocates of HGE set out their stall. At the symposium, which was attended by nearly 1,000 people, James Watson, of DNA discovery fame, advocated the use of HGE not merely for medical purposes, but for 'enhancement': 'And the other thing, because no one really has the guts to say it, I mean, if we could make better human beings by knowing how to add genes, why shouldn't we do it?'
In his recent book, Re-Making Eden (1998), Princeton biologist, Lee Silver celebrates the coming future of human 'enhancement', in which the health, appearance, personality, cognitive ability, sensory capacity, and life-span of our children all become artifacts of genetic engineering, literally selected from a catalog. Silver acknowledges that the costs of these technologies will limit their full use to only a small 'elite', so that over time society will segregate into the "GenRich" and the "Naturals":
"The GenRich - who account for 10 percent of the American population - all carry synthetic genes... that were created in the laboratory ...All aspects of the economy, the media, the entertainment industry, and the knowledge industry are controlled by members of the GenRich class...Naturals work as low-paid service providers or as labourers, and their children go to public schools... If the accumulation of genetic knowledge and advances in genetic enhancement technology continue ... the GenRich class and the Natural class will become...entirely separate species with no ability to cross-breed, and with as much romantic interest in each other as a current human would have for a chimpanzee."
Silver, another speaker at the UCLA symposium, believes that these trends should not and cannot be stopped, because to do so would infringe on liberty.
Most scientists say that what is preventing them from embarking on HGE is the risk that the process will itself generate new mutations, which will be passed on to future generations. Official scientific and ethical bodies tend to rely on this as the basis for forbidding attempts at HGE, rather than any principled opposition to the idea.
In my view, we should not allow ourselves to be lulled into a false sense of security by this argument. Experience with genetically engineered crops, for example, shows that we are unlikely ever to arrive at a situation when we can be sure that the risks are zero. Instead, when scientists are ready to proceed, we will be told that the risks are 'acceptable', compared to the benefits. Meanwhile, there will be people telling us loudly that since they are taking the risks with their children, we have no right to interfere.
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Human Genetics Alert - The Threat of Human Genetic Engineering
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Cryonics – Wikipedia, the free encyclopedia
Posted: at 9:56 pm
For the study of the production of very low temperatures, see Cryogenics. For the low-temperature preservation of living tissue and organisms in general, see Cryopreservation. For the Hot Cross album, see Cryonics (album).
Cryonics (from Greek 'kryos-' meaning 'icy cold') is the low-temperature preservation of animals and humans who cannot be sustained by contemporary medicine, with the hope that healing and resuscitation may be possible in the future.[1][2]
Cryopreservation of people or large animals is not reversible with current technology. The stated rationale for cryonics is that people who are considered dead by current legal or medical definitions may not necessarily be dead according to the more stringent information-theoretic definition of death.[3] It is proposed that cryopreserved people might someday be recovered by using highly advanced technology.[4]
Some scientific literature supports the feasibility of cryonics.[4][5] An open letter supporting the idea of cryonics has been signed by 63 scientists, including Aubrey de Grey and Marvin Minsky.[6] However, many other scientists regard cryonics with skepticism.[7] As of 2013, approximately 270 people have undergone cryopreservation procedures since cryonics was first proposed in 1962.[8][9] In the United States, cryonics can only be legally performed on humans after they have been pronounced legally dead, as otherwise it would be considered murder or assisted suicide.[10]
Cryonics procedures ideally begin within minutes of cardiac arrest, and use cryoprotectants to prevent ice formation during cryopreservation.[11] However, the idea of cryonics also includes preservation of people long after legal death because of the possibility that brain structures that encode memory and personality may still persist and be inferable in the future. Whether sufficient brain information still exists for cryonics to successfully preserve may be intrinsically unprovable by present knowledge.[12] Therefore, most proponents of cryonics see it as an intervention with prospects for success that vary widely depending on circumstances.
A central premise of cryonics is that long-term memory, personality, and identity are stored in durable cell structures and patterns within the brain that do not require continuous brain activity to survive.[13] This premise is generally accepted in medicine; it is known that under certain conditions the brain can stop functioning and still later recover with retention of long-term memory.[14][15] Additional scientific premises of cryonics[16] are that (1) brain structures encoding personality and long-term memory persist for some time after legal death, (2) these structures are preserved by cryopreservation, and (3) future technologies that could restore encoded memories to functional expression in a healed person are theoretically possible. At present only cells, tissues, and some small organs can be reversibly cryopreserved.[17][18]
Cryonics advocates say it is possible to preserve the fine cell structures of the brain in which memory and identity reside with present technology.[19] They say that demonstrably reversible cryopreservation is not necessary to achieve the present-day goal of cryonics, which is preservation of brain information that encodes memory and personal identity. They say current cryonics procedures can preserve the anatomical basis of mind,[11] and that this should be sufficient to prevent information-theoretic death until future repairs might be possible.[20]
A moral premise of cryonics is that all terminally ill patients should have the right, if they so choose, to be cryopreserved.[21] Some cryonicists believe as a matter of principle that anyone who would ordinarily be regarded as dead should instead be made a "permanent patient" subject to whatever future advances might bring.[22]
Long-term cryopreservation can be achieved by cooling to near 77.15 Kelvin (approximately -196.01C), the boiling point of liquid nitrogen. It is a common mistaken belief that cells will lyse (burst) due to the formation of ice crystals within the cell, since this only occurs if the freezing rate exceeds the osmotic loss of water to the extracellular space.[23] However, damage from freezing can still be serious; ice may still form between cells, causing mechanical and chemical damage. Cryonics organizations use cryoprotectants to reduce this damage. Cryoprotectant solutions are circulated through blood vessels to remove and replace water inside cells with chemicals that prevent freezing. This can reduce damage greatly,[24] but freezing of the entire body still causes injuries that are not reversible with present technology. The difficulties of recovering complex organisms from a frozen state have been long known. Attempts to recover large frozen mammals by simply rewarming were abandoned by 1957.[25]
When used at high concentrations, cryoprotectants stop ice formation completely. Cooling and solidification without crystal formation is called vitrification.[26] The first cryoprotectant solutions able to vitrify at very slow cooling rates while still being compatible with tissue survival were developed in the late 1990s by cryobiologists Gregory Fahy and Brian Wowk for the purpose of banking transplantable organs.[27][28] These solutions were adopted for use in cryonics by the Alcor Life Extension Foundation, for which they are believed to permit vitrification of some parts of the human body, especially the brain.[29] This has allowed animal brains to be vitrified, warmed back up, and examined for ice damage using light and electron microscopy. No ice crystal damage was found.[20][30] The Cryonics Institute also uses a vitrification solution developed by their staff cryobiologist, Yuri Pichugin, applying it principally to the brain.[31]
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How Cryonics Works – HowStuffWorks
Posted: at 9:56 pm
The year is 1967. A British secret agent has been "frozen," awaiting the day when his arch nemesis will return from his own deep freeze to once again threaten the world. That day finally arrives in 1997. The agent is revived after 30 years on ice, and he saves the world from imminent destruction.
You'll probably recognize this scenario from the hit movie, "Austin Powers: International Man of Mystery" (1997). Cryonics also shows up in films like "Vanilla Sky" (2001), "Sleeper" (1973) and "2001: A Space Odyssey" (1968). But is it pure Hollywood fiction, or can people really be frozen and then thawed to live on years later?
The science behind the idea does exist. It's called cryogenics -- the study of what happens to materials at really low temperatures. Cryonics -- the technique used to store human bodies at extremely low temperatures with the hope of one day reviving them -- is being performed today, but the technology is still in its infancy.
In this article, we'll look at the practice of cryonics, learn how it's done and find out whether humans really can be brought back from the deep freeze.
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