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3D printing has has a presence in the medical industry since the 1980s for modelling body parts that are otherwise untouchable without invasive surgery, but research into the potential of this technology is bringing clinicians closer to getting a good look up close at the real thing. Instead of scans, what about injecting a camera no bigger than a grain of salt into your patient?

A group of German researchers have been working on a complex lens system that is small enough to fit inside a syringe, and applications aren’t just limited to the medical industry. They have the potential to also be used in many products which need parts to be as small and light as possible, such as drones and smart phones.

syringe-camera-4

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Two interconnected brain areas — the hippocampus and the entorhinal cortex — help us to know where we are and to remember it later. By studying these brain areas, researchers at Baylor College of Medicine, Rice University, The University of Texas MD Anderson Cancer Center and the National Cancer Institute have uncovered new information about how dysfunction of this circuit may contribute to memory loss in Alzheimer’s disease. Their results appear in Cell Reports.

“We created a new mouse model in which we showed that spatial memory decays when the entorhinal cortex is not functioning properly,” said co-corresponding author Dr. Joanna Jankowsky, associate professor of neuroscience at Baylor. “I think of the entorhinal area as a funnel. It takes information from other sensory cortices — the parts of the brain responsible for vision, hearing, smell, touch, and taste — and funnels it into the . The hippocampus then binds this disparate information into a cohesive memory that can be reactivated in full by recalling only one part. But the hippocampus also plays a role in spatial navigation by telling us where we are in the world. These two functions converge in the same cells, and our study set out to examine this duality.”

The new mouse model was genetically engineered to carry a particular surface receptor on the cells of the entorhinal cortex. When this receptor was activated by administering the drug ivermectin to the mice, the cells of the entorhinal cortex silenced their activity. They stopped funnelling information to the hippocampus. This system allowed the scientists to turn off the entorhinal cortex, and to determine how this affected hippocampal function.

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A drink containing liquid aspirin could extend the lives of thousands of brain cancer patients, according to breakthrough research.

British experts have found that the simple drug can cross the ‘blood-brain barrier’ — a hurdle which has so far stopped cancer drugs attacking brain tumours.

Scientists will today announce the results of early tests which show liquid aspirin is ten times more effective than any existing chemotherapy at killing brain cancer cells.

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With a radio specifically designed to communicate through tissue, Professors David Blaauw (http://web.eecs.umich.edu/faculty/blaauw/) and David Wentzloff (http://web.eecs.umich.edu/~wentzlof/) from the University of Michigan’s Electrical and Computer Engineering Department (https://www.eecs.umich.edu/ece/) are adding another level to a computer platform small enough to fit inside a medical grade syringe.

With this enabling technology, real time information can be applied to devices monitoring heart fibrillation as well as glucose monitoring for diabetics.

This new radio, designed by Graduate Student Research Assistant Yao Shi, can transmit information from inside the body up to one foot to a data base receiver, more than 5 times the distance from any known radio of equal size.

ABOUT THE PROFESSORS

Different species of animals either live a very long time or do not die of old age. Some cases are the tortoise & lobster species that live to be over 130 years old naturally and don’t usually die unless they get sick or are killed.

After we grow up our cells ultimately stop self-replicating. A researcher named Leonard Hayflick figured out that each of our cells divide around 50 times and then they stop. Once all of our cells stop duplicating we start to deteriorate and then ultimately die. This finding showed that we are in fact programmed to die biologically.

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Its painful to bear views that make many think I’m an imbicile and dislike me. So please, if anybody has a rational argument why any of this is wrong, I beg to be enlightened. I’ve set up a diagram for the purpose that will support you to add your criticism exactly where it is pertinent. https://tssciencecollaboration.com/graphtree/Are%20Vaccines%20Safe/406/4083

(1) The National Academy’s Reviews Of Vaccine Safety
The Institute of Medicine of the National Academies has provided several multi-hundred page surveys studying the safety of vaccines, but rather than reassuring, these itemize some iatrogenic conditions being caused, and pronounce the scientific literature inadequate to say whether most others are. The 2011 Institute of Medicine (IOM) Review[1] looked at 146 vaccine-condition pairs for causality, reporting:

  • 14 for which the evidence is said to convincingly support causality, the vaccine is causing the condition.
  • 4 where the evidence is said to favor acceptance.
  • 5 where the evidence is said to favor rejection, including MMR causing autism.
  • 123 where the evidence is said insufficient to evaluate.

The 2003 IOM Review on multiple vaccines said[2]:
“The committee was unable to address the concern that repeated exposure of a susceptible child to multiple immunizations over the developmental period may also produce atypical or non-specific immune or nervous system injury that could lead to severe disability or death (Fisher, 2001). There are no epidemiological studies that address this.”
and:
“the committee concludes that the epidemiological and clinical evidence is inadequate to accept or reject a causal relationship between multiple immunization and an increased risk of allergic disease, particularly asthma.”

  • None of the IOM Safety Reviews[1][2][3][4] addressed the aluminum (for example whether the aluminum is causing autism), or mentioned contaminants, or discussed animal models although they had concluded as just quoted there is generally no epidemiological or clinical data worth preferring.

(2) The Aluminum.
Alum was added to vaccines back in the 1920’s, with no test of parenteral toxicity until recently[5], because it prods the immature immune system out of its normal operating range.[6] Maybe they figured aluminum is common in the environment, but injection bypasses half a dozen evolved sequential filters that normally keep it out of circulatory flow during development. Vaccines put hundreds of times as much aluminum into infants’ blood as they would otherwise get, and in an unnatural form that is hard for the body to remove.[7][8 (cfsec 4.2)][9]. The published empirical results indicate its highly toxic.

  • Bishop et al in NEJM 97 reported a Randomized Placebo Controlled(RPC) test on preemies.[10][11] Scaling the toxicity they measured to the 4000 mcg in the first six months projects the vaccine series’ aluminum as costing each recipient maybe 15 IQ points and bone density.[12]
  • Animal RPC experiments also show highly toxic[13][14][15][16]
  • The applicable epidemiology suggests its highly toxic.[8][18][19][20][21][22] Discussed more in point 8 below, basically every study that compares more to less finds less much better.
  • Numerous clinical publications, whole special issues, on ASIA (Autoimmune Syndrome Induced by Adjuvants)[23][24][25]
  • Any “placebo” controlled test I’ve ever found of an adjuvanted vaccine, the “placebo” contained an adjuvant.
  • Safety reviews ignore the issue. Search the pdfs. [1][2][3][4]
  • The FDA[26] cites a theory paper[27] that compares a published MRL based on dietary experiments in weaned rodents (thus completely uninformed about toxicity in early development) to a theoretical model of blood aluminum levels from the vaccines, and disdains all the above cited empirical evidence.

(3) The Safety Studies Ignore Confounding Patient Behavior
Since there are no Randomized Placebo Controlled (RPC) trials supporting vaccines, virtually all studies report on the association (or lack thereof) between vaccines and some iatrogenic condition. But parents who believe vaccines made their kids sick, stop vaccinating them, which systematically moves sick or vaccine damaged kids in the studies into the “low vaccine”, “low thimerisol”, or etc. bin. This invalidates most studies supporting safety (and the few remaining ones suck for other reasons). Numerous studies report incredible preventative effects for vaccines, presumably because of this corruption, like having more thimerisol or more MMR’s is strongly preventative of autism and other mental development issues[28][29][30], or like having more vaccines was strongly preventative of atopy, apparently even years before patients got the vaccines[31]. The fact this confounding factor is overlooked demonstrates extreme confirmation bias and is the defining factor of Cargo Cult Science according to R.P. Feynman.[32]

(4) The Animal Models
Animal models reliably and repeatably show in RPC tests (a) that vaccines at the wrong time in development damage the adult brain or behavior [33][34] and (b) that multiple vaccines cause autoimmune disease even in animals bred to be non-autoimmune[35][36]. The effects are said to be robust, and as we’ve already seen there isn’t good human data rebutting them.

(5) The Contaminants
Studies have repeatedly found contaminants such as viruses, retroviruses, circoviruses, and human DNA in vaccines seemingly whenever tested,
and I’ve found no reason to believe off the shelf vaccines are free[37][38][39][40][41]. Reported contaminants have included SV-40 in polio vaccines which were administered even though scientists knew the vaccines were contaminated and already had hunches and experiments indicating SV-40 causes cancer[41][42]. Chimpanzee Coryza Virus became known in humans as RSV and has killed many millions of infants and hospitalizes 100,000/yr in America today[43]. Contaminated polio vaccine is plausibly also the origin of HIV[44][41]. There are discovered viral contaminants in vaccines today[38][39], with unknown long term effects, as well as I expect many undiscovered contaminants.

(6) Studies Ask Whether Some One Vaccine Damages, and Thus Miss That Many Do.
Virtually every study not reporting damage compares kids who got numerous vaccines to kids who got numerous vaccines. Such studies wouldn’t show statistically significant results no matter how much damage the vaccines are doing, unless one vaccine or vector by itself is doing comparable or more damage than the rest put together. The studies more or less test the hypothesis one vaccine is invisibly damaging, the rest are fine, and the studies are all obscured in the presence of multiple problems, much less the kind of timing and interaction effects observed in animal models. The one study[45] often touted as proving “The Risk of Autism is Not Increased by ‘Too Many Vaccines Too Soon’”[46] in fact compares patients based on antigens, and since DTP had more than 3000 antigens and no other vaccine common among the study patients had more than a handful, effectively compared patients who’d had DTP and dozens of vaccines to patients who did not have DTP (many had DTaP instead) and dozens of vaccines. The only counterexamples to this I’ve found are contrived in bizarre ways to avoid reality, such as the study that withheld the 2 month vaccines till 3 months from a group of kids, and asked the mothers, who were terrified enough a bunch insisted on changing back to the early vaccination group, to record symptoms with no doctor even consulted, identifying the placebo effect as vaccine prevention of diseases. The authors wrote it would have been unethical to give a placebo at 2 months to the kids getting the vaccine at 3 months, in order to do the experiment blind, but apparently consider it ethical to inject dozens of vaccines into your kids with zero placebo controlled testing.[47] [48]

(7) The Extensive Evidence Indicating Flu Vaccines Damage Immune Systems, Particularly in Children.

It is good to see production costs v. value add return comparisons with drugs as part of an ongoing drive to create drugs cheaper and making them cheaper to patients. However, lets do not sacrifice quality (especially in areas like cancer, MS, etc.) for costs of development/ cost savings. Value of life is priceless.


Defining the value of a drug in relation to its cost and benefit is an emerging theme in cancer care but remains untested.

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A new UK study has identified a gene signature that predicts poor survival from ovarian cancer. The study also identified genes which help the cancer develop resistance to chemotherapy — offering a new route to help tackle the disease.

The study, published in the International Journal of Cancer, examined the role of HOX genes in ovarian cancer resistance and whether a drug known as HXR9 which targets HOX, could help prevent the resistance from developing.

The HOX gene family enables the remarkably rapid cell division seen in growing embryos. Most of these genes are switched off in adults, but previous research has shown that in several cancers, including ovarian cancer, HOX genes are switched back on, helping the cancer cells to proliferate and survive.

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Glad they are doing something on this because my biggest concern on biometrics and systems storing other people’s DNA/ bio information is criminals hacking in and collecting bio information on people and reselling it on the Dark Web. With this type of information; criminals can do many interesting things especially if they have access to a gene editing kit, or 3D printers, etc. We have seen how easy it is to create gene editing kits and selling them on the net for $129 each. And, how 3D printers can replicate synthetic skin, contacts mimicking eye structures, etc. So, criminals can do some amazing things once they have access to anyone’s biometrics information.


A biometric system to verify travelers exiting the country could be in effect as soon as 2018.

By Kayla Nick-Kearney.

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Excellent start in using GPU for mapping and predictive analysis on brain functioning and reactions; definitely should prove interesting to medical & tech researchers and engineers across the board should find this interesting.


MIS Asia offers Information Technology strategy insight for senior IT management — resources to understand and leverage information technology from a business leadership perspective.

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