Alex Jones Show - David Icke: Human Genetics, Paedophile Gov., The Religion of Death
Tuesday November 6th 2012 Alex talks with author and presenter David Icke about Election fraud, Paedophiles in the Government Royals, plus human Genetics. http://www.davidicke.com Alex Jones Show Complete Playlist: http://www.youtube.com Infowars Nightly News Complete Playlist: http://www.youtube.com Infowars Special Reports Playlist: http://www.youtube.com http://www.infowars.com http://www.prisonplanet.tv http://www.prisonplanet.com httpFrom:AlexJonesCompleteViews:184 9ratingsTime:01:00:04More inNews Politics

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Alex Jones Show - David Icke: Human Genetics, Paedophile Gov., The Religion of Death - Video

Human Genetics, The Religion of Death : David Icke
David Icke Human Genetics, The Religion of Death Follow InfoWars Live twitter.com Alex Jones InfoWars ! Did you watch David Icke on Wembley Arena october 27 2012 ? watch - youtube.com Follow InfoWars Live twitter.comFrom:InfoWarsLiveViews:36 1ratingsTime:58:00More inNews Politics

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Human Genetics, The Religion of Death : David Icke - Video

BLINDNESS (The Hidden)
#9658; #9658; #9658; Enjoy the video? Subscribe! bit.ly #9668; #9668; #9668; Download Here: http://www.hidden-source.com What is The Hidden? "In the early 1950s human genetics experimentation was taking its first, tentative steps. Amongst many other black projects, a team of British scientists working at an Infinitum Research experimental station stumbled across some remarkable phenomena involving DNA manipulation. This led to deeper research with dangerously unpredictable results, often leading to human patients losing their lives in irresponsible and immoral experiments. Time passed on, and by the mid 1990s the failure rate of the experiments had been reduced from 75% to a mere 15%, enough for Infinitum to move onto the next stage Biological Light Refraction. The British team were hoping to unravel the possibilities of light manipulation to create the perfect covert military agent. Early into the new millennium, due to a gross miscalculation, a series of tests on Subject 617 led to a massive synaptic trauma leaving the patient with multiple genetic anomalies. The subject was left in constant pain and with unstable DNA. The subject escaped captivity, killing anyone that got in its way. The IRIS (Infinitum Research Interception Squad) team have been deployed to return the subject to a maximum security Infinitum Research facility for further study and dissection. The entire project was considered a failure: all funding ceased and development was discontinued while all records and traces of the experiments ...From:SeaNannersViews:163784 6695ratingsTime:03:01More inGaming

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BLINDNESS (The Hidden) - Video

Public release date: 8-Nov-2012 [ | E-mail | Share ]

Contact: Cathy Yarbrough press@ashg.org 858-243-1814 American Society of Human Genetics

A team of researchers at Kaiser Permanente and the University of California, San Francisco (UCSF) has identified a significant relationship between mortality and the length of telomeres, the stretches of DNA that protect the ends of chromosomes, according to a presentation on Nov. 8 at the American Society of Human Genetics 2012 meeting in San Francisco.

While a reduction in telomere length is regarded as a biomarker of aging, scientists have not yet determined whether it plays a direct causal role in aging-related health changes and mortality or is just a sign of aging.

In their prospective study of 100,000 multi-ethnic individuals whose average age was 63 years, the researchers determined that an association between telomere length and mortality existed and persisted even after the data were adjusted for such demographic and behavioral factors as education, smoking and alcohol consumption, said Catherine Schaefer, Ph.D., director of the Kaiser Permanente (KP) Research Program on Genes, Environment and Health (RPGEH).

Dr. Schaefer and Neil Risch, Ph.D., director of the UCSF Institute for Human Genetics, are principal investigators of the Genetic Epidemiology Research Study on Adult Health and Aging (GERA). UCSF professor and Nobel laureate Elizabeth Blackburn, Ph.D., led the research on telomere length measurement.

The telomere research, part of the GERA project, has genotyped over 675,000 markers of 100,000 KP Northern California patients and linked them with health data from their electronic medical records. To obtain DNA for genotyping and telomere measurement, the researchers collected saliva samples from the patients, who volunteered for the project and provided scientists with access to their electronic medical records.

Two years prior to the saliva collection, the researchers conducted a detailed survey of the patients' demographic and behavioral factors, providing a unique opportunity to address questions of telomere epidemiology and aging.

"With these data, we examined demographic relationships with telomere length, behavioral influences and relationship of telomere length with all causes of mortality following sample collection," said Dr. Schaefer. "Although we found that shorter-than-average telomeres were prospectively associated with mortality, only those with the shortest telomeres were at increased risk of death."

Dr. Risch added, "While this could indicate a direct effect of telomere length on health, it will also be important to examine the extent of pre-existing diseases in these individuals to understand their possible role in the biological connection between telomere length and longevity."

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Significant relationship between mortality and telomere length discovered

Alex Jones on David Icke 2001 - The Turd
Alex Jones #39; view on David Icke in 2001 was very different than it is now. It looks like these two alleged conspiracy conmen have reached an entente cordiale for the purposes of cross promotion. http://www.infoderp.com This is a response to "David Icke: Human Genetics, The Religion of Death"From:infoderpViews:7 0ratingsTime:02:42More inNews Politics

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Alex Jones on David Icke 2001 - The Turd - Video

Public release date: 8-Nov-2012 [ | E-mail | Share ]

Contact: Cathy Yarbrough press@ashg.org 858-243-1814 American Society of Human Genetics

A consortium of scientists who are taking a novel approach in their research to detect the genetic variations that predispose individuals to type 2 diabetes provided an update of their findings at the American Society of Human Genetics (ASHG) 2012 meeting.

Among the project's novel characteristics is the ethnic diversity of the 10,000 individuals whose exomes, the 18,000 protein-coding genes, are being sequenced.

The researchers recruited 5,000 individuals with type 2 diabetes (T2D) from five major ancestry groups: African-American, East Asian, European, Hispanic and South Asian. The study population also includes an equal number of controls, individuals from these same ancestry groups who do not have T2D.

"Our hypothesis is that screening the exome in a range of diverse ethnic groups increases the range of variants of each gene surveyed, and thereby improves our ability to detect genes showing differences in the patterns of the DNA codes for proteins between individuals with type 2 diabetes and controls," said T.M. Teslovich, Ph.D., research fellow in statistical genetics at the University of Michigan, who presented the study at ASHG 2012.

The study is one of the three projects under the umbrella of the NIH-sponsored T2D-GENES (Type 2 Diabetes Genetic Exploration by Next-generation sequencing in multi-Ethnic Samples) study.

The scientists' approach also will enable them to determine whether there are T2D risk variants that are unique to an ancestry group.

An initial analysis of the data on 3,500 African-American, East Asian and South Asian individuals identified about 1.6 million single nucleotide variants (SNVs), 71.5% of which were previously unknown.

"Only about 89,000, or 5.6%, of the 1.6 million variants are present in all three groups," said Dr. Teslovich.

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Novel type 2 diabetes genetic study involves 5 major ancestry groups

Public release date: 8-Nov-2012 [ | E-mail | Share ]

Contact: Cathy Yarbrough press@ashg.org 858-243-1814 American Society of Human Genetics

About 10.6% of the inherited genetic risk for developing coronary artery disease (CAD) can be explained by specific DNA variations, according to research reported today at the American Society of Human Genetics 2012 meeting.

The research, conducted by scientists in the CARDIoGRAMplusC4D consortium, pinpointed 20 previously unidentified mutations during a two-stage meta-analysis of 63,746 patients with CAD, which causes more deaths worldwide than any other disease.

These genetic variants generally were infrequently found in the DNA of the 130,681 individuals without heart disease who were in the control group.

The new mutations have boosted to 47 the total number of DNA variants that have thus far been linked to an increased risk for developing CAD, said Panos Deloukas, Ph.D., who co-led the study and heads the Genetics of Complex Traits in Humans research group at the Wellcome Trust Sanger Institute, Cambridge, UK.

Scientists had previously estimated that 30 to 60% of the variation in CAD might be attributable to genetic risk factors, according to a study published in 2005*. The research reported at ASHG 2012 expands the number of specific genes that are likely involved.

"We no longer assume that coronary heart disease is triggered by just a handful of genes, each with a strong effect on a person's risk for the disease," said Dr. Deloukas. "Our research supports the current assumption that heart disease risk is determined by a large group of genes, each with a modest effect on risk."

Identifying the genetic mutations that set the stage for CAD enables researchers to investigate the underlying mechanisms of the disease, which may lead to therapeutic targeting through drugs, he said.

Many of the newly identified variations are in genes that operate in biological pathways involved in the body's metabolism of lipids or fats as well as in inflammation.

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DNA variants explain over 10 percent of inherited genetic risk for heart disease

Public release date: 8-Nov-2012 [ | E-mail | Share ]

Contact: Cathy Yarbrough press@ashg.org 858-243-1814 American Society of Human Genetics

A research team reported that next generation sequencing of the exome, the 1 to 2% of the DNA containing the genes that code for proteins, enabled the identification of the genetic causes of unexplained intellectual disability in over 50% of patients in a study conducted at Radboud University Medical Centre in Nijmegen, The Netherlands.

"Through next generation sequencing, we were able to discover mutations in genes that had not been previously linked to causing intellectual disability," said Marjolein Willemsen, M.D., Ph.D., who presented the research today (Nov. 8) at the American Society of Human Genetics 2012 meeting in San Francisco.

Correctly diagnosing children with intellectual disability (ID) can lead to early intervention and special education programs, vocational training and health screenings for associated conditions that will enable them to reach their full potential, said Dr. Willemsen of Radboud's department of human genetics.

Genetic diagnosis "is of major importance for the care and counseling of patients and families," Dr. Willemsen said. "Proper diagnosis provides insight into associated health and behavioral problems, prognosis and recurrence risk."

The cause of intellectual disability is unknown in more than half of patients with learning and other intellectual disabilities, which affect about 2% of the population, said Tjitske Kleefstra, M.D., Ph.D., also of Radboud University Medical Centre's human genetics department.

Participating in the Radboud University study were 253 patients with unexplained intellectual disability, most of whom were adults. They underwent a multidisciplinary clinical evaluation and a metabolic screen. Genome-wide analysis of each patient's DNA was also conducted, and specific genetic diagnostic tests were performed as needed.

Because they used both genetic tests and clinical evaluations, the researchers were able to correlate the biological as well as the behavioral features of each patient's intellectual disability with the DNA findings.

Intellectual disability can be a challenge to diagnose because a wide range of features characterizes these disorders, and the underlying genetic causes can vary widely, Dr. Kleefstra said. "As a result, many parents go from one doctor to another in search of a diagnosis and treatment for their child," she added.

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Unexplained intellectual disability explained by state-of-the-art genetic analysis

ScienceDaily (Nov. 8, 2012) Research findings confirming that de novo mutations represent a major cause of previously unexplained intellectual disability were presented on Nov. 8 at the American Society of Human Genetics 2012 meeting in San Francisco.

Josep de Ligt, M.Sc., bioinformatician and Ph.D. student in human genetics at Radboud University Nijmegen Medical Centre in The Netherlands, also reported findings lending support to the use of exome sequencing, which deciphers over 21,000 protein-coding genes and not the entire human genome, as a diagnostic assay to determine whether one or more genetic mutations explain a patient's intellectual disability.

The cause of intellectual disability, which represents a wide range of phenotypes, or observable biological characteristics, is unknown in at least 50% of patients.

Most individuals with intellectual disability without a known cause are the only members of their families with the condition. Because the cause of their child's cognitive impairment is unknown, parents are often baffled.

The child with a cognitive disability is often an "isolated case without family history of the condition," said de Ligt, adding that intellectual disability occurs in about 1% of the population,

By exome sequencing of 100 patients with unexplained cognitive impairment, de Ligt and his colleagues uncovered 79 genes with unique de novo mutations.

These de novo mutations were present in the DNA of the patients but not in that of their parents whose exomes also were sequenced.

"All de novo as well as X-linked mutations identified in this study were interpreted in the context of the clinical diagnosis," de Ligt pointed out.

The diagnostic interpretation revealed that 16 of the 100 mutations were causative, or pathogenic. Ten of these mutations occurred in genes already known to be involved in intellectual disability, and three X-linked maternally-inherited mutations were identified.

In addition, de novo mutations were uncovered in three novel candidate genes, which after follow-up were found to be more frequently mutated in patients with intellectual disability.

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Exome sequencing: Potential diagnostic assay for unexplained intellectual disability

The 10000 Year Explosion: How Civilization Accelerated Human Evolution - , Henry Harpending
ll4.me The 10000 Year Explosion: How Civilization Accelerated Human Evolution - , Henry Harpending Resistance to malaria. Blue eyes. Lactose tolerance. What do all of these traits have in common? Every one of them has emerged in the last 10000 years. Scientists have long believed that the ?great leap forward #65533; that occurred some 40000 to 50000 years ago in Europe marked end of significant biological evolution in humans. In this stunningly original account of our evolutionary history, top scholars Gregory Cochran and Henry Harpending reject this conventional wisdom and reveal that the human species has undergone a storm of genetic change much more recently. Human evolution in fact accelerated after civilization arose, they contend, and these ongoing changes have played a pivotal role in human history. They argue that biology explains the expansion of the Indo-Europeans, the European conquest of the Americas, and European Jews #39; rise to intellectual prominence. In each of these cases, the key was recent genetic change: adult milk tolerance in the early Indo-Europeans that allowed for a new way of life, increased disease resistance among the Europeans settling America, and new versions of neurological genes among European Jews.Ranging across subjects as diverse as human domestication, Neanderthal hybridization, and IQ tests, Cochran and Harpending #39;s analysis demonstrates convincingly that human genetics have changed and can continue to change much more rapidly than ...From:anthony bishopViews:2 0ratingsTime:00:11More inPeople Blogs

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The 10000 Year Explosion: How Civilization Accelerated Human Evolution - , Henry Harpending - Video

Protein Structural Biology In Biomedical Research. Advances In Molecular And Cell Biology, Volume 22
ll4.me Protein Structural Biology In Biomedical Research. Advances In Molecular And Cell Biology, Volume 22b. Recent advances in protein structural biology, coupled with new developments in human genetics, have opened the door to understanding the molecular basis of many metabolic, physiological, and developmental processes in human biology. Medical pathologies, and their chemical therapies, are increasingly being described at the molecular level. For single-gene diseases, and some multi-gene conditions, identification of highly correlated genes immediately leads to identification of covalent structures of the actual chemical agents of the disease, namely the protein gene products. Once the primary sequence of a protein is ascertained, structural biologists work to determine its three-dimensional, biologically active structure, or to predict its probable fold and/or function by comparison to the data base of known protein structures. Similarly, three-dimensional structures of proteins produced by microbiological pathogens are the subject of intense study, for example, the proteins necessary for maturation of the human HIV virus. Once the three-dimensional structure of a protein is known or predicted, its function, as well as potential binding sites for drugs that inhibit its function, become tractable questions. The medical ramifications of the burgeoning results of protein structural biology, from gene replacement therapy to rational drug design, are well recognized by ...From:ashleygibbons986Views:0 0ratingsTime:00:14More inPeople Blogs

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Protein Structural Biology In Biomedical Research. Advances In Molecular And Cell Biology, Volume 22 - Video

Growth Hormone
ll4.me Growth Hormone Introduction.- Placenta and early embryonic development.- Experimental models.- Evolution, aging, life span.- Brain development.- Development of sensory organs.- Neuroplasticity and neuroprotection.- Reproductive tract.- Skeletal muscle.- Cardiovascular system-lung.- Hematopoiesis.- Pancreas development and glucose regulation.- IGF interaction with other trophic factors.- Cancer.- Human genetics of the GH-IGF-I axis.- Future perspectives-stem cells.- Index EAN/ISBN : 9780387262741 Publisher(s): Springer, Berlin, Springer US Discussed keywords: Wachstumshormon Format: ePub/PDF Author(s): Varela-Nieto, Isabel - Chowen, Julie A. Introduction.- Placenta and early embryonic development.- Experimental models.- Evolution, aging, life span.- Brain development.- Development of sensory organs.- Neuroplasticity and neuroprotection.-From:lamarpalmer654Views:0 0ratingsTime:00:14More inPeople Blogs

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Growth Hormone - Video

GHOST ISLAND (The Hidden)
#9658; #9658; #9658; Enjoy the video? Subscribe! bit.ly #9668; #9668; #9668; Download Here: http://www.hidden-source.com What is The Hidden? "In the early 1950s human genetics experimentation was taking its first, tentative steps. Amongst many other black projects, a team of British scientists working at an Infinitum Research experimental station stumbled across some remarkable phenomena involving DNA manipulation. This led to deeper research with dangerously unpredictable results, often leading to human patients losing their lives in irresponsible and immoral experiments. Time passed on, and by the mid 1990s the failure rate of the experiments had been reduced from 75% to a mere 15%, enough for Infinitum to move onto the next stage Biological Light Refraction. The British team were hoping to unravel the possibilities of light manipulation to create the perfect covert military agent. Early into the new millennium, due to a gross miscalculation, a series of tests on Subject 617 led to a massive synaptic trauma leaving the patient with multiple genetic anomalies. The subject was left in constant pain and with unstable DNA. The subject escaped captivity, killing anyone that got in its way. The IRIS (Infinitum Research Interception Squad) team have been deployed to return the subject to a maximum security Infinitum Research facility for further study and dissection. The entire project was considered a failure: all funding ceased and development was discontinued while all records and traces of the experiments ...From:SeaNannersViews:279982 9717ratingsTime:03:17More inGaming

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GHOST ISLAND (The Hidden) - Video

The Hidden - (Fart Grenades And Friendly Fire)
#9689; #9689; #9689; #9658;Did you like the video? Why not Subscribe! bit.ly #9689; #9689; #9689; #9658;If you enjoy why not leave a like/comment and let me know? #9668; #9689; #9689; #9689; In the early 1950s human genetics experimentation was taking its first, tentative steps. Amongst many other black projects, a team of British scientists working at an Infinitum Research experimental station stumbled across some remarkable phenomena involving DNA manipulation. This led to deeper research with dangerously unpredictable results, often leading to human patients losing their lives in irresponsible and immoral experiments. Time passed on, and by the mid 1990s the failure rate of the experiments had been reduced from 75% to a mere 15%, enough for Infinitum to move onto the next stage: Biological Light Refraction. The British team were hoping to unravel the possibilities of light manipulation to create the perfect covert military agent. Early into the new millennium, due to a gross miscalculation, a series of tests on Subject 617 led to a massive synaptic trauma leaving the patient with multiple genetic anomalies. The subject was left in constant pain and with unstable DNA. The subject escaped captivity, killing anyone that got in its way. The IRIS (Infinitum Research Interception Squad) team have been deployed to return the subject to a maximum security Infinitum Research facility for further study and dissection. The entire project was considered a failure: all funding ceased and development was discontinued while all records and ...From:Dustin RushViews:15 1ratingsTime:17:59More inGaming

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The Hidden - (Fart Grenades And Friendly Fire) - Video

GHOST ISSUES (The Hidden)
Download: grabups.com "In the early 1950s human genetics experimentation was taking its first, tentative steps. Amongst many other black projects, a team of British scientists working at an Infinitum Research experimental station stumbled across some remarkable phenomena involving DNA manipulation. This led to deeper research with dangerously unpredictable results, often leading to human patients losing their lives in irresponsible and immoral experiments. Time passed on, and by the mid 1990s the failure rate of the experiments had been reduced from 75% to a mere 15%, enough for Infinitum to move onto the next stage: Biological Light Refraction. The British team were hoping to unravel the possibilities of light manipulation to create the perfect covert military agent. Early into the new millennium, due to a gross miscalculation, a series of tests on Subject 617 led to a massive synaptic trauma leaving the patient with multiple genetic anomalies.From:bifurcarsb05Views:2 0ratingsTime:03:21More inGaming

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GHOST ISSUES (The Hidden) - Video

The Hidden - (Blood For The Blood God, I Must Feed)
#9689; #9689; #9689; #9658;Did you like the video? Why not Subscribe! bit.ly #9689; #9689; #9689; #9658;If you enjoy why not leave a like/comment and let me know? #9668; #9689; #9689; #9689; In the early 1950s human genetics experimentation was taking its first, tentative steps. Amongst many other black projects, a team of British scientists working at an Infinitum Research experimental station stumbled across some remarkable phenomena involving DNA manipulation. This led to deeper research with dangerously unpredictable results, often leading to human patients losing their lives in irresponsible and immoral experiments. Time passed on, and by the mid 1990s the failure rate of the experiments had been reduced from 75% to a mere 15%, enough for Infinitum to move onto the next stage: Biological Light Refraction. The British team were hoping to unravel the possibilities of light manipulation to create the perfect covert military agent. Early into the new millennium, due to a gross miscalculation, a series of tests on Subject 617 led to a massive synaptic trauma leaving the patient with multiple genetic anomalies. The subject was left in constant pain and with unstable DNA. The subject escaped captivity, killing anyone that got in its way. The IRIS (Infinitum Research Interception Squad) team have been deployed to return the subject to a maximum security Infinitum Research facility for further study and dissection. The entire project was considered a failure: all funding ceased and development was discontinued while all records and ...From:Dustin RushViews:1 0ratingsTime:19:06More inGaming

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The Hidden - (Blood For The Blood God, I Must Feed) - Video

Evening with the UC Davis Genome Center - Oct 6, 2012 - David Segal
Modern human genetics and genomics are revolutionizing biology, medicine, and society. Genomic technology is now advancing faster than computer technology. The day is rapidly approaching when individuals will be able to obtain their entire personal genetic sequence. Is society ready? Should we have access to this information? While it may inform us of our susceptibility to some diseases much earlier, will it improve health or simply reveal our fate? At this Evening with the UC Davis Genome Center event David Segal, addresses these timely questions and discusses the potential impact that this new technology could have on public health, as well as some ways this information can be used and protected.From:David SegalViews:2 0ratingsTime:01:00:58More inScience Technology

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Evening with the UC Davis Genome Center - Oct 6, 2012 - David Segal - Video

David Icke: Human Genetics, The Religion of Death
Alex talks with author and presenter David Icke about election fraud and human genetics. http://www.davidicke.com ORDER THIS SURVIVAL DVD AND START GETTING PREPARED TODAY AT... http://www.infowarsshop.com Joel Skousen sits down with Alex Jones and discusses strategies on how to prepare for and survive major disasters. http://www.infowars.com http://www.prisonplanet.tv twitter.com http://www.facebook.com [Join The Alex Jones Team and Start Getting Healthy Today!] http://www.infowarsteam.com Get all your Youngevity Products such as Beyond Tangy Tangerine, the Alex Pack and Pollen Burst. These supplements are a great way to get your essentials vitamins, minerals, amino acids, and other beneficial nutrients [[[ProPur Water Filtration]]] http://www.infowarsshop.comFrom:TheAlexJonesChannelViews:8627 245ratingsTime:58:00More inPeople Blogs

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David Icke: Human Genetics, The Religion of Death - Video

David Icke - Infowars Election Coverage 2012
Alex Jones talks with author and presenter David Icke about election fraud and human genetics. http://www.davidicke.com http://www.infowars.com prisonplanet.tv conspiracyscope.blogspot.com http://www.youtube.comFrom:ConspiracyScopeViews:518 13ratingsTime:58:00More inNews Politics

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David Icke - Infowars Election Coverage 2012 - Video

David Icke Exposes ROYAL PAEDOPHILES
Alex talks with author and presenter David Icke about election fraud and human genetics. .From:sswemmerViews:17 2ratingsTime:58:00More inEducation

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David Icke Exposes ROYAL PAEDOPHILES - Video