Posts Tagged ‘Science’

Scientists Allege By: Dr. Cyril Broderick, Professor of Plant Pathology Dear World Citizens: I have read a number of articles from your Internet outreach as well as articles from other sources about the casualties in Liberia and other West African countries about the human devastation caused by the Ebola virus. About a week ago, I read an article published in the Internet news summary publication of the Friends of Liberia that said that there was an agreement that the initiation of the Ebola outbreak in West Africa was due to the contact of a two-year old child with bats that had flown in from the Congo. That report made me disconcerted with the reporting about Ebola, and it stimulated a response to the “Friends of Liberia,” saying that African people are not ignorant and gullible, as is being implicated. A response from Dr. Verlon Stone said that the article was not theirs, and that “Friends of Liberia” was simply providing a service. He then asked if he could publish my letter in their Internet forum. I gave my permission, but I have not seen it published. Because of the widespread loss of life, fear, physiological trauma, and despair among Liberians and other West African citizens, it is incumbent that I make a contribution to the resolution of this devastating situation, which may continue to recur, if it is not properly and adequately confronted. I will address the situation in five (5) points: 1. EBOLA IS A GENETICALLY MODIFIED ORGANISM (GMO) Horowitz (1998) was deliberate and unambiguous when he explained the threat of new diseases in his text, Emerging Viruses: AIDS and Ebola – Nature, Accident or Intentional. In his interview with Dr. Robert Strecker in Chapter 7, the discussion, in the early 1970s, made it obvious that the war was between countries that hosted the KGB and the CIA, and the ‘manufacture’ of ‘AIDS-Like Viruses’ was clearly directed at the other. In passing during the Interview, mention was made of Fort Detrick, “the Ebola Building,” and ‘a lot of problems with strange illnesses’ in “Frederick [Maryland].” By Chapter 12 in his text, he had confirmed the existence of an American Military-Medical-Industry that conducts biological weapons tests under the guise of administering vaccinations to control diseases and improve the health of “black Africans overseas.” The book is an excellent text, and all leaders plus anyone who has interest in science, health, people, and intrigue should study it. I am amazed that African leaders are making no acknowledgements or reference to these documents. 2. EBOLA HAS A TERRIBLE HISTORY, AND TESTING HAS BEEN SECRETLY TAKING PLACE IN AFRICA I am now reading The Hot Zone, a novel, by Richard Preston (copyrighted 1989 and 1994); it is heart-rending. The prolific and prominent writer, Steven King, is quoted as saying that the book is “One of the most horrifying things I have ever read. What a remarkable piece of work.” As a New York Times bestseller, The Hot Zone is presented as “A terrifying true story.” Terrifying, yes, because the pathological description of what was found in animals killed by the Ebola virus is what the virus has been doing to citizens of Guinea, Sierra Leone and Liberia in its most recent outbreak: Ebola virus destroys peoples’ internal organs and the body deteriorates rapidly after death. It softens and the tissues turn into jelly, even if it is refrigerated to keep it cold. Spontaneous liquefaction is what happens to the body of people killed by the Ebola virus! The author noted in Point 1, Dr. Horowitz, chides The Hot Zone for writing to be politically correct; I understand because his book makes every effort to be very factual. The 1976 Ebola incident in Zaire, during President Mobutu Sese Seko, was the introduction of the GMO Ebola to Africa. 3. SITES AROUND AFRICA, AND IN WEST AFRICA, HAVE OVER THE YEARS BEEN SET UP FOR TESTING EMERGING DISEASES, ESPECIALLY EBOLA The World Health Organization (WHO) and several other UN Agencies have been implicated in selecting and enticing African countries to participate in the testing events, promoting vaccinations, but pursuing various testing regiments. The August 2, 2014 article, West Africa: What are US Biological Warfare Researchers Doing in the Ebola Zone? by Jon Rappoport of Global Research pinpoints the problem that is facing African governments. Obvious in this and other reports are, among others: (a) The US Army Medical Research Institute of Infectious Diseases (USAMRIID), a well-known centre for bio-war research, located at Fort Detrick, Maryland; (b) Tulane University, in New Orleans, USA, winner of research grants, including a grant of more than $7 million the National Institute of Health (NIH) to fund research with the Lassa viral hemorrhagic fever; (c) the US Center for Disease Control (CDC); (d) Doctors Without Borders (also known by its French name, Medicins Sans Frontiers); (e) Tekmira, a Canadian pharmaceutical company; (f) The UK’s GlaxoSmithKline; and (g) the Kenema Government Hospital in Kenema, Sierra Leone. Reports narrate stories of the US Department of Defense (DoD) funding Ebola trials on humans, trials which started just weeks before the Ebola outbreak in Guinea and Sierra Leone. The reports continue and state that the DoD gave a contract worth $140 million dollars to Tekmira, a Canadian pharmaceutical company, to conduct Ebola research. This research work involved injecting and infusing healthy humans with the deadly Ebola virus. Hence, the DoD is listed as a collaborator in a “First in Human” Ebola clinical trial (NCT02041715, which started in January 2014 shortly before an Ebola epidemic was declared in West Africa in March. Disturbingly, many reports also conclude that the US government has a viral fever bioterrorism research laboratory in Kenema, a town at the epicentre of the Ebola outbreak in West Africa. The only relevant positive and ethical olive-branch seen in all of my reading is that Theguardian.com reported, “The US government funding of Ebola trials on healthy humans comes amid warnings by top scientists in Harvard and Yale that such virus experiments risk triggering a worldwide pandemic.” That threat still persists. 4. THE NEED FOR LEGAL ACTION TO OBTAIN REDRESS FOR DAMAGES INCURRED DUE TO THE PERPETUATION OF INJUSTICE IN THE DEATH, INJURY AND TRAUMA IMPOSED ON LIBERIANS AND OTHER AFRICANS BY THE EBOLA AND OTHER DISEASE AGENTS. The U. S., Canada, France, and the U. K. are all implicated in the detestable and devilish deeds that these Ebola tests are. There is the need to pursue criminal and civil redress for damages, and African countries and people should secure legal representation to seek damages from these countries, some corporations, and the United Nations. Evidence seems abundant against Tulane University, and suits should start there. Yoichi Shimatsu’s article, The Ebola Breakout Coincided with UN Vaccine Campaigns, as published on August 18, 2014, in the Liberty Beacon. 5. AFRICAN LEADERS AND AFRICAN COUNTRIES NEED TO TAKE THE LEAD IN DEFENDING BABIES, CHILDREN, AFRICAN WOMEN, AFRICAN MEN, AND THE ELDERLY. THESE CITIZENS DO NOT DESERVE TO BE USED AS GUINEA PIGS! Africa must not relegate the Continent to become the locality for disposal and the deposition of hazardous chemicals, dangerous drugs, and chemical or biological agents of emerging diseases. There is urgent need for affirmative action in protecting the less affluent of poorer countries, especially African citizens, whose countries are not as scientifically and industrially endowed as the United States and most Western countries, sources of most viral or bacterial GMOs that are strategically designed as biological weapons. It is most disturbing that the U. S. Government has been operating a viral hemorrhagic fever bioterrorism research laboratory in Sierra Leone. Are there others? Wherever they exist, it is time to terminate them. If any other sites exist, it is advisable to follow the delayed but essential step: Sierra Leone closed the US bioweapons lab and stopped Tulane University for further testing. The world must be alarmed. All Africans, Americans, Europeans, Middle Easterners, Asians, and people from every conclave on Earth should be astonished. African people, notably citizens more particularly of Liberia, Guinea and Sierra Leone are victimized and are dying every day. Listen to the people who distrust the hospitals, who cannot shake hands, hug their relatives and friends. Innocent people are dying, and they need our help. The countries are poor and cannot afford the whole lot of personal protection equipment (PPE) that the situation requires. The threat is real, and it is larger than a few African countries. The challenge is global, and we request assistance from everywhere, including China, Japan, Australia, India, Germany, Italy, and even kind-hearted people in the U.S., France, the U.K., Russia, Korea, Saudi Arabia, and anywhere else whose desire is to help. The situation is bleaker than we on the outside can imagine, and we must provide assistance however we can. To ensure a future that has less of this kind of drama, it is important that we now demand that our leaders and governments be honest, transparent, fair, and productively engaged. They must answer to the people. Please stand up to stop Ebola testing and the spread of this dastardly disease. Thank you very much. Sincerely, Dr. Cyril E. Broderick, Sr. About the Author: Dr. Broderick is a former professor of Plant Pathology at the University of Liberia’s College of Agriculture and Forestry. He is also the former Observer Farmer in the 1980s. It was from this column in our newspaper, the Daily Observer, that Firestone spotted him and offered him the position of Director of Research in the late 1980s. In addition, he is a scientist, who has taught for many years at the Agricultural College of the University of Delaware. Source: http://www.liberianobserver.com/security/ebola-aids-manufactured-western-pharmaceuticals-us-dod

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“Control the oil, and you control nations. Control the food, and you control the people.”* -Henry Kissenger

Genetic Engineering is the direct manipulation of the coding sequence, or genome, within the cell of an organism. It proceeds by taking genetic information found within the DNA molecule and tampering with it, by inserting new genetic information. The organism that develops from this newly formed DNA strand will typically have different traits and characteristics from those which would have formed from the untampered DNA.

The application of this technology has resulted in tobacco resistant to a virus, the Flavr Savr tomato, with its lengthened shelf life, and a variety of crops developed to be resistant to herbicides.

This week’s episode of the Global Research News Hour features contributions by Saskatchewan-based writer, researcher and former Saskatchewan Green Party leader Sandra Finley, bio-diversity activist Vandana Shiva, and writer and geo-political analyst F. William Engdahl.

Listen to the show: CLICK HERE

Download MP3 of  the show CLICK HERE

The public generally resists knowingly consuming foods made from genetically modified organisms (GMOs). Much of the controversy around GMOs rests in the ability of biotech companies like Monsanto to patent them and charge royalties for their use.

For millennia, farmers have saved seeds and replanted them year after year. Now, farmers on top of other stresses around climate, controlling pests and coping with global competition must contend with a model of agriculture that increases their overhead while compromising the sustainability of their yields.

How do the laws of supply and demand economics come into play when there seems to be no public appetite (pardon the pun) for this technology?

This week’s episode of the Global Research News Hour features contributions by Saskatchewan-based writer, researcher and former Saskatchewan Green Party leader Sandra Finley, bio-diversity activist Vandana Shiva, and writer and geo-political analyst F. William Engdahl.

Sandra Finley touches on her observations in the changes in farming and community life in rural Saskatchewan as a result of the introduction of modern chemical intensive agriculture methods. As well, she outlines the corrosive effect biotech partnerships are having on research in our universities.

Vandana Shiva, scientist, author, ecologist and outspoken critic of GMOs speaks about impacts in the developing world, particularly India, where farmers have had biotech seeds imposed on them and in desperation are taking their own lives by the tens of thousands.

William Engdahl is the author of the 2007 book Seeds of Destruction: The Hidden Agenda of Genetic Manipulation. He outlines GMO agriculture’s links to eugenics, the Rockefellers and a motivation to corner the market on food production.

View original source: Centre for research on globalization

http://patft.uspto.gov/netacgi/nph-Parser?Sect2=PTO1&Sect2=HITOFF&p=1&u=%2Fnetahtml%2FPTO%2Fsearch-bool.html&r=1&f=G&l=50&d=PALL&RefSrch=yes&Query=PN%2F4647773 Method of continuous production of retroviruses (HTLV-III) from patients with AIDS and pre-AIDS Abstract A cell system is disclosed for the reproducible detection and isolation of human T-lymphotropic retroviruses (HTLV-family) with cytopathic effects (HTLV-III) from patients with the acquired immune deficiency syndrome (AIDS), pre-AIDS and in healthy carriers. One neoplastic aneuploid T-cell line derived from an adult with lymphoid leukemia, and termed HT, was susceptible to infection with the new variants of HTLV, which are transformed and providing T-cell populations which are highly susceptible and permissive from HTLV-III, and convenience for large scale production, isolation and biological detection of the virus. Inventors: Gallo; Robert C. (Bethesda, MD), Popovic; Mikulas (Bethesda, MD) Assignee: The United States of America as represented by the Department of Health (Washington, DC) [*] Notice: The portion of the term of this patent subsequent to May 28, 2002 has been disclaimed. Appl. No.: 06/602,946 Filed: April 23, 1984 Current U.S. Class: 435/239 ; 424/208.1; 435/235.1; 435/372.3; 435/948 Current International Class: C12N 5/06 (20060101); C12N 7/00 (20060101); C12N 007/02 (); C12N 007/00 (); C12N 005/00 (); C12R 001/91 () Field of Search: 435/235,239,240,948,5,29 424/89 128/1T References Cited [Referenced By] U.S. Patent Documents 4464465 August 1984 Lostrom et al. 4520113 May 1985 Gallo et al. Other References Popovic et al, Science, 224(4648):497-500, May 4, 1984. . Gallo et al, “Isolation of Human T-Cell Leukemia Virus in Acquired Immune Deficiency Syndrome (AIDS)”, Science, 220, pp. 865-867 (5-1983). . Barre-Sinoussi et al, “Isolation of a T-Lymphotropic Retrovirus from a Patient at Risk for AIDS”, Science, 220, pp. 868-871 (5-1983). . Marx, “Strong New Candidate for AIDS Agent”, Science, 224, pp. 475-477 (5-1984).. Primary Examiner: Warren; Charles F. Assistant Examiner: Tarcza; John Edward Attorney, Agent or Firm: Roberts, Jr.; John S. Claims We claim: 1. A method for continuous production of HTLV-III virus which comprises infecting in cell culture highly susceptible, permissive cells consisting of a neoplastic aneuploid HT-cell line with said virus, said cells preserve the capacity for permanent growth after the infection with said virus, growing said cells under conditions suitable for cell growth and recovering said virus produced by said cells. 2. The method of claim 1, wherein said virus consists of cytopathic variants of HTLV. 3. The method of claim 1 wherein said infecting comprises cocultivating said virus with said cells to produce a cell line and recovering said cell line. 4. The method of claim 1 wherein said infecting comprises cell-free infection of said cells with said virus. 5. The method of claim 1 wherein said cells are neoplastic aneuploid T-cells derived from an adult with lymphoid leukemia. 6. A process for the continuous production of HTLV-III virus which comprises cocultivating said virus with a target HT-cell to produce an infected cell line, growing said cell line and recovering said virus from supernatants produced by said cell line. 7. The process of claim 6 wherein said target T-cell is a neoplastic aneuploid T-cell susceptible to infection with HTLV-III. 8. A process for the continual production of HTLV-III by infecting T-cells in cultures which comprises cocultivating HTLV-III virus with an HT-clone to produce an infected cell line, said clone being an aneuploid T-cell line derived from lymphoid leukemia, growing said cell line and recovering said virus from supernatants produced by said cell line. 9. The process in claim 8 wherein said clone is a mature T-cell phenotype of OKT3.sup.+ (62%), OKT4.sup.+ (39%) and OKT8.sup.-. 10. A method of producing a cell line containing an antigen of HTLV-III which comprises infecting an HT-cell line derived from lymphoid leukemia and susceptible to infection with HTLV-III, said cell line is capable of continuous large-scale production of HTLV-III, and growing the infected cell line under conditions suitable for growth. 11. The method of claim 10 wherein said cell line is a neoplastic aneuploid T-cell line. 12. The method of claim 10 wherein said HTLV-III are variants of human T-lymphotropic retrovirus, exhibit cytopathic effects and are non-transforming. 13. A cell line containing HTLV-III designated H9/HTLV-III.sub.B, ATCC Accession CRL 8543. 14. A process for producing a cell line H9/HTLV-III.sub.B which comprises infecting a target T-cell with HTLV-III virus to produce a cell line and recovering same, said infecting process overcomes the normal cytopathic effect of HTLV-III and preserves the immortal growth capacity of the target cell. 15. An HT cell line permanently infected with HTLV-III virus, wherein said cell line continually produces said virus. Description The present invention describes a cell system for the reproducible detection and isolation of human T-lymphotropic retroviruses (HTLV-family) with cytopathic or cell killing effects (HTLV-III) from patients with the acquired immune deficiency syndrome (AIDS), pre-AIDS and in healthy carriers. One neoplastic aneuploid T-cell line derived from an adult with lymphoid leukemia, and termed HT, was susceptible to infection with the new variants of HTLV, providing T-cell populations which are highly susceptible and permissive for HTLV-III, and convenience for large scale production, isolation, and biological detection of the virus. BACKGROUND OF THE INVENTION The disclosure of this invention is contained in the following journal articles: Gallo et al., “Detection, Isolation, and Continuous Production of Cytopathic Human T-Lymphotropic Retroviruses (HTLV-III) from Patients with AIDS and pre-AIDS,” Science, in press; and Gallo et al., “Human T-Lymphotropic Retrovirus, HTLV-III, Isolated from AIDS Patients and Donors at Risk for AIDS,” in press. Epidemiologic data strongly suggest that acquired immune deficiency syndrome (AIDS) is caused by an infectious agent which is apparently horizontally transmitted by intimate contact or blood products. Though the disease is manifested by opportunistic infections, predominantly Pneumocystis carcinii pneumonia and Kaposi’s sarcoma, the underlying disorder affects the patient’s cell-mediated immunity with absolute lymphopenia and reduced helper T-lymphocyte (OKT4.sup.+) subpopulation(s). Moreover, before a complete clinical manifestation of the disease occurs, its prodrome, pre-AIDS, is frequently characterized by unexplained chronical lymphadenopathy and/or leukopenia involving a helper T cell subset. This leads to the severe immune deficiency of the patient, suggesting that a specific subset of T-cells is the primary target for an infectious agent. Although patients with AIDS or pre-AIDS are often chronically infected with cytomegalovirus or hepatitis B virus, for various reasons these appear to be opportunistic or coincidental infections apparently not linked to the immunological response deficiency. It is believed that the cause of AIDS may be a virus from the family of human T-cell lymphotropic retroviruses (HTLV) which, prior to the present invention, comprised two major well characterized subgroups of human retroviruses, called human T-cell leukemia/lymphoma viruses, HTLV-I and HTLV-II. The most common isolate, HTLV-I, is mainly obtained from patients with mature T-cell malignancies. Seroepidemiological studies, in vitro biological effects, and nucleic acid hybridization data indicate that HTLV-I is etiologically associated with these malignancies, affecting adults primarily in the south of Japan, the Caribbean and Africa. HTLV of subgroup II (HTLV-II) was first isolated from a patient with a T-cell variant of hairy cell leukemia. To date, this is the only reported isolate of HTLV-II from a patient with a neoplastic disease. Virus isolation and seroepidemiological data show that HTLV of both subgroups can sometimes be found in patients with AIDS. Evidence suggests that the retrovirus(es) of the HTLV family is an etiological agent of AIDS based on the following: (1) there is precedence for an animal retrovirus cause of immune deficiency (feline leukemia virus in cats); (2) retroviruses of the HTLV family are T-cell tropic; (3) they preferentially infect “helper” T-cells (OKT4.sup.+); (4) they have cytopathic effects on various human and mammalian cells as demonstrated by their induction of cell syncytia formation; (5) they can alter some T-cell functions; (6) in some cases infection may result in selective T-cell killing; and (7) they are transmitted by intimate contact or through blood products. The presence of antibodies directed to cell membrane antigens of HTLV infected cells has been shown in sera of more than 40% of patients with AIDS [Essex et al., Science, 220:859 (1983)]. This antigen has since been defined as part of the envelope of HTLV [Schupbach, et al., Science, in press; and Lee, et al., Proc. Nat. Acad. Sci. U.S.A., in press]. The original detection and isolation of the various HTLV isolates were made possible by two earlier developments: the discovery of T-cell growth factor (TCGF), also called Interleukin 2 (Il-2), which enabled the routine selective growth of different subsets of normal and neoplastic mature T-cells [Ruscetti, et al., J. Immunol., 119:131 (1977); and Poiesz, et al., Proc. Nat. Acad. Sci. U.S.A, 77:6134 (1980)] and the development of sensitive assays for detection of retroviruses based on reverse transcriptase assays. The methods of HTLV isolation and transmission involved a cocultivation procedure using permissive T-cells for the virus. The use of normal human T-cells in cocultivation experiments preferentially yielded HTLV of both subgroups with immortalizing (transforming) capability for some of the target T-cells. However, HTLV variants (now termed HTLV-III), lack immortalizing properties for normal T-cells and mainly exhibit cytopathic effects on the T-cells and is now believed to be the cause of AIDS. In fact, such variants were frequently but only transiently detected using these normal T-cells as targets in cocultivation or cell-free transmission experiments. The cytopathic effect was overcome by finding a highly susceptible, permissive cell for cytopathic variants of HTLV, thus preserving the capacity for permanent growth after infection with the virus. The present invention discloses the identification and characterization of this new immortalized T-cell population and its use in the isolation and continuous high- level production of such viruses from patients with AIDS and pre-AIDS. Early experiments identified one neoplastic aneuploid T-cell line, termed HT, derived from an adult with lymphoid leukemia, that was susceptible to infection with the new cytopathic virus isolates. This cell line is a sensitive target for transmission of these virus isolates (HTLV-III) and it allows continuous large-scale virus production and development of specific immunologic reagents and nucleic acid probes useful for comparison of these new isolates among themselves and with HTLV-I and HTLV-II. In addition to their differences in biological effects that distinguish them from HTLV-I and HTLV-II, HTLV-III also differs from these known HTLV subgroups in several immunological assays and in morphology. However, these new retroviruses are T4 lymphotropic and exhibit many properties similar to HTLV-I and II, including similar properties of the reverse transcriptase, cross reactivity of structural proteins as determined by heterologous competition radioimmune assays with patients’ sera and with animal hyperimmune sera, and induction of syncytia. These new retrovirus isolates are collectively designated HTLV-III, together with detectable differences in some of their proteins and genetic information, HTLV-III’s ability to kill T-cells clearly separates these variants from other members of the HTLV family. Read the full patent via the US patent website

http://www.redicecreations.com/article.php?id=19957 Factions of three of the largest governments in the world—the United States of America, the Russian Federation, and the Peoples Republic of China—may be cutting orders to eliminate a man who they see as one of the most dangerous in the world. No, he’s not the world’s most hunted multi-national terrorist, nor even a mad scientist with a new virus that can wipe out humanity. The most dangerous man in the world may be Brazilian physicist Dr. Fran De Aquino. De Aquino [right] hasn’t developed a death ray or obtained secret launch codes to the world’s nuclear missiles. He’s done something potentially much worse: he’s spilled the scientific and technological beans of the greatest secret in the world: the ultimate purpose of HAARP. A brilliant physicist published a revolutionary paper citing 30 other scientific papers that reveal HAARP has incredible powers far beyond what most investigators of the high frequency energy technology suspect. Dr. Fran De Aquino asserts a fully functional HAARP network, activated globally, can not only affect weather and geophysical events, but influence space and gravity…even time itself! Now the network is almost complete with the activation of the newest HAARP facilities at the bottom of the world: the desolate and alien Antarctic. Will the masters of HAARP become the masters of time too? HAARP (High Frequency Active Auroral Research Program) now has installations criss-crossing the world and extends from pole-to-pole. The Antarctic facilities are near completion. De Aquino, whose paper High-power ELF radiation generated by modulated HF heating of the ionosphere can cause earthquakes, cyclones and localized heating [PDF], lifts the veil hiding the HAARP wizards… Read the full report & download pdf here

The Extinction Protocol

December 14, 2012CALIFORNIAScientists have discovered one of the world’s weirdest volcanoes on the seafloor near the tip of Baja, Mexico. The petite dome — about 165 feet tall (50 meters) and 4,000 feet long by 1,640 feet wide (1,200 m by 500 m) — lies along the Alarcón Rise, a seafloor-spreading center. Tectonic forces are tearing the Earth’s crust apart at the spreading center, creating a long rift where magma oozes toward the surface, cools and forms new ocean crust. Circling the planet like baseball seams, seafloor-spreading centers (also called mid-ocean ridges) produce copious amounts of basalt, a low-silica content lava rock that makes up the ocean crust. But samples from the newly discovered volcano are strangely rhyolite lava, and have the highest silica content (up to 77 percent) of any rocks collected from a mid-ocean ridge, said Brian Dreyer, a geochemist at the University of…

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PN

by Dave Mihalovic, Prevent Disease
Waking Times
December 8, 2012

WIKI-Nanofiber-300x259Bill Gates is at it again, throwing money at any researcher with a claim to fame and everything to gain by using scientific advances to prevent as many babies as possible from being born. Soft kill drugs in the pretext of protection is the common theme for the Bill and Melinda Gates Foundation. Cheap, effective contraceptive and HIV pharmaceuticals are now the objectives soon to target the third world.

A University of Washington team has developed a platform they say simultaneously offers contraception and prevents HIV. Electrically spun cloth with nanometer-sized fibers can dissolve to release drugs, providing a platform for cheap medical use. The research was published this week in the Public Library of Science’s open-access journal PLoS One. The Bill & Melinda Gates Foundation last month awarded the UW researchers almost $1 million to pursue the technology.

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earth change affirmations

A discourse on the aspect of Sacred Geometry known as Metatron’s Cube by Charles Gilchrist.
Sacred Geometry is the eternal visual language wrapped around the root concepts of the manifest universe.…Metatron’s Cube is a tremendously important aspect of Nature’s First Pattern; it is based on 13 circles found within  this pattern. Connecting the centers of these 13 circles is the key…LINK

www.earthchangesaffirmations.com

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The Extinction Protocol

September 26, 2012RUSSIARussian authorities temporary suspended the import and sale of Monsanto’s genetically-modified corn after a French study suggested it may be linked to cancer. ­The Russia’s consumer-rights regulator Rospotrebnadzor asked scientists at the country’s Institute of Nutrition to review the study. The watchdog has also contacted to European Commission’s Directorate General for Health & Consumers to explain the EU’s position on GM corn. The report prepared by France’s University of Caen and published last week, claimed that rats fed over a two-year period with Monsanto’s genetically modified NK603 corn, developed more tumors and other pathologies than a test group fed with regular corn. The NK603, sold under the Roundup label, is genetically engineered to withstand glyphosate weed killer. The company criticized the study, saying it “doesn’t meet minimum acceptable standards for this type of scientific research” and the data was incomplete. Monsanto also said Russia’s…

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earth change affirmations

The ‘chorus’ phenomenon is well known by scientists, which is a cluster of brief, rising-frequency tones that sound like the chorus of birds singing at sunrise. Energetic particles in the magnetosphere emit radio waves that are audible to humans. Recently launched NASA Radiation Belt Storm Probes mission’s (RBSP) instrumentation captured an instance of the event…LINK to video

www.earthchangesaffirmations.com

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earth change affirmations

According to study published in the New Scientist back in 1998, there is a direct connection between the Sun’s solar storms and human biological effects.

The conduit which facilitates the charged particles from the Sun to human disturbance — is the very same conduit which steers Earth’s weather —– the magnetic field. Animals and humans have a magnetic field which surrounds them — in the very same way the magnetic field surrounds the Earth as a protector…LINK

www.earthchangesaffirmations.com

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Biotech company needlessly uses aborted human fetal cells to test artificial food flavors

Tuesday, April 12, 2011 by: Ethan Huff

(NaturalNews) Senomyx, a San Diego, Cal.-based biotechnology company that specializes in food flavoring ingredients, is under fire for allegedly using aborted human fetal cells to test the effectiveness of its various synthetic flavoring agents. According to reports, the company has plenty of other viable options at its disposal for testing such ingredients that do not involve the moral and ethical problems associated with using aborted human fetal cells, but for whatever reason it has ignored pleas to stop using them.
The Senomyx website explains that the company develops “savory, sweet and salt flavor ingredients that are intended to allow for the reduction of MSG (monosodium glutamate), sugar and salt in food and beverage products.” But the way in which it does this is through the use of “isolated human taste receptors,” which a group called Children of God for Life (CGL) suggests is a deceptive marketing term to cover up their true nature.

“What they don’t tell the public is that they are using HEK 293 — human embryonic kidney cells taken from an electively aborted baby to produce those receptors,” said Debi Vinnedge, director of CGL. “They could have easily chosen animal, insect, or other morally obtained human cells expressing the G protein for taste receptors.”

CGL says it has tried to contact Senomyx on numerous occasions to urge the company to switch to alternative testing methods, but has yet to receive a formidable response. CGL has also contacted many of the company’s “collaborators,” which include PepsiCo, Kraft Foods, Solae, and Nestle. Such collaborators help fund research and development at Senomyx, as well as pay royalties on sales of products they sell that include the company’s flavor ingredients.

Campbell Soup was also a Senomyx collaborator, but shortly after being contacted by CGL, the company indicated that it had officially cut ties with Senomyx over the ordeal.

Besides the company’s questionable use of aborted fetal cells to test its flavors, the flavors themselves are synthetically-derived. Artificial flavor enhancers are exactly what their name insinuates — fake. They typically reduce costs for processed food producers by extending flavors and tastes but provide no nutritional benefit to consumers.

[Editor`s Note: NaturalNews is strongly against the use of all forms of animal testing. We fully support implementation of humane medical experimentation that promotes the health and wellbeing of all living creatures.]

Sources for this story include:

http://www.lifenews.com/2011/03/29/company-uses-fetal-cells-from-abor…

http://www.onenewsnow.com/Culture/Default.aspx?id=1320092

http://www.naturalnews.com/022982.html

Learn more: http://www.naturalnews.com/032043_human_fetal_cells_artificial_flavors.html#ixzz27QtOW8qI

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Obama agency rules Pepsi’s use of aborted fetal cells in soft drinks constitutes ‘ordinary business operations’

Saturday, March 17, 2012 by: Ethan A. Huff, staff writer

(Blogging as most people have missed this important report, if your drinking pepsi, read this.)-AA

Learn more: http://www.naturalnews.com/035276_Pepsi_fetal_cells_business_operations.html#ixzz27QseOFEn

The Obama Administration has given its blessing to PepsiCo to continue utilizing the services of a company that produces flavor chemicals for the beverage giant using aborted human fetal tissue. LifeSiteNews.com reports that the Obama Security and Exchange Commission (SEC) has decided that PepsiCo’s arrangement with San Diego, Cal.-based Senomyx, which produces flavor enhancing chemicals for Pepsi using human embryonic kidney tissue, simply constitutes “ordinary business operations.”

The issue began in 2011 when the non-profit group Children of God for Life (CGL) first broke the news about Pepsi’s alliance with Senomyx, which led to massive outcry and a worldwide boycott of Pepsi products. At that time, it was revealed that Pepsi had many other options at its disposal to produce flavor chemicals, which is what its competitors do, but had instead chosen to continue using aborted fetal cells — or as Senomyx deceptively puts it, “isolated human taste receptors”

A few months later, Pepsi’ shareholders filed a resolution petitioning the company to “adopt a corporate policy that recognizes human rights and employs ethical standards which do not involve using the remains of aborted human beings in both private and collaborative research and development agreements.”
But the Obama Administration shut down this 36-page proposal, deciding instead that Pepsi’s used of aborted babies to flavor its beverage products is just business as usual, and not a significant concern.

“We’re not talking about what kind of pencils PepsiCo wants to use — we are talking about exploiting the remains of an aborted child for profit,” said Debi Vinnedge, Executive Director of CGL, concerning the SEC decision. “Using human embryonic kidney (HEK-293) to produce flavor enhancers for their beverages is a far cry from routine operations!”

To be clear, the aborted fetal tissue used to make Pepsi’s flavor chemicals does not end up in the final product sold to customers, according to reports — it is used, instead, to evaluate how actual human taste receptors respond to these chemical flavorings. But the fact that Pepsi uses them at all when viable, non-human alternatives are available illustrates the company’s blatant disregard for ethical and moral concerns in the matter.

Back in January, Oklahoma Senator Ralph Shortey proposed legislation to ban the production of aborted fetal cell-derived flavor chemicals in his home state. If passed, S.B. 1418 would also reportedly ban the sale of any products that contain flavor chemicals derived from human fetal tissue, which includes Pepsi products as well as products produced by Kraft and Nestle
Source: NaturalNews

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