or disease could change the impedance properties of the wearer wrist, requiring the device to be recalibrated,
and the stress this can put on the power grid. But Solar City believes that if building huge factories to produce advanced solar panels can bring down costs,
First Emotion-Reading Apps for Kids with Autism The first mobile apps that use emotion-reading software to help kids with autism are nearing release,
Though the early academic research focused on applications such as helping people with autism, so far the technology has been used commercially to help marketers understand
We started out with research on autism, and we went out and did this commercial stuff.
and apply it back to autism again. The advertising work helped make the software more accurate by rainingit
to use brain implants to read, and then control, the emotions of mentally ill people. This week the Defense Advanced Research Projects Agency,
or DARPA, awarded two large contracts to Massachusetts General Hospital and the University of California, San francisco,
to create electrical brain implants capable of treating seven psychiatric conditions, including addiction, depression, and borderline personality disorder.
The project builds on expanding knowledge about how the brain works; the development of microlectronic systems that can fit in the body;
The U s. faces an epidemic of mental illness among veterans, including suicide rates three or four times that of the general public.
But drugs and talk therapy are limited of use which is why the military is turning to neurological devices,
says Justin Sanchez, manager of the DARPA program, known as Subnets, for Systems-Based Neurotechnology for Emerging Therapies. e want to understand the brain networks in neuropsychiatric illness,
develop technology to measure them, and then do precision signaling to the brain, says Sanchez. t something completely different and new.
Companies including the medical device giant Medtronic and startup Cortera Neurotechnologies a spin out from UC Berkeley wireless laboratory,
More recently, doctors have used such stimulators to treat severe cases of obsessive-compulsive disorder (see rain Implants Can Reset Misfiring Circuits.
the U s. Food & Drug Administration approved Neuropace, the first implant that both records from the brain and stimulates it (see apping Seizures Away.
It is used to watch for epileptic seizures and then stop them with electrical pulses. Altogether, U s. doctors bill for about $2. 6 billion worth of neural stimulation devices a year, according to industry estimates.
Researchers say they are making rapid improvements in electronics, including small, implantable computers. Under its program, Mass General will work with Draper Laboratories in Cambridge, Massachusetts,
who have created several prototypes of miniaturized brain implants. Michel Maharbiz, a professor in Berkeley electrical engineering department, says the Obama brain initiative,
wee trying to build the next generation of psychiatric brain stimulators, says Alik Widge, a researcher on the Mass General team.
a psychiatrist who directs Mass General division of neurotherapeutics, says one aim could be to extinguish fear in veterans with posttraumatic stress disorder, or PTSD.
Fear is generated in the amygdala part of the brain involved in emotional memories. But it can be repressed by signals in another region,
like relaxation or anxiety, using implants he called timoceivers. But Delgado, also funded by the military,
Psychiatric implants would in fact control how mentally ill people act, although in many cases indirectly, by changing how they Feel for instance,
Dougherty says a brain implant would only be considered for patients truly debilitated by mental illness, and who can be helped with drugs
let do surgery, says Dougherty. t going to be for people who don respond to the other treatments. o
#Genome Editing to Reverse Bubble Boy Syndrome Researchers used an emerging technique to correct the gene behind a fatal immune system disorder in an infant.
Genome editing technology is considered a promising new tool for curing disease. For decades gene therapy has meant that a virus delivers a functional copy of a gene that is dysfunctional in a patient.
and the therapeutic version typically remains separate from the rest of the genome. The technology has drawbacks.
First, by sitting outside of the genome, the activity of therapeutic gene isn regulated properly.
In some cases, the therapeutic copy is delivered by a retrovirus the plunks the new gene down near randomly in the patients genome,
Second, some diseases, such as Huntington can be treated this way because the broken copy of the gene causes harm.
Using genome editing to repair genes could circumvent these issues (see enome Surgery. In the new study, published today in the journal Nature,
researchers in Milan treated a condition known as Severe Combined Immunodeficiency Syndrome, or SCID (this condition is referred sometimes to as ubble boy diseasebecause children afflicted may live in protected environments
because the risk of death from infectious disease is extremely likely). Children with this genetic condition have been treated with the additive gene therapy method in the past,
and some suffered leukemia-like diseases as a side effect (see he Glimmering Promise of Gene therapy.
Scientists used zinc fingers to engineer the immune cells of patients with HIV to resist the virus (see an Gene therapy Cure HIV?.
#DNA-Based Research May have unveiled Long-Sought Diabetes Treatment A synthetic drug that controls blood sugar in obese mice demonstrates the potential of a DNA-dependent method for developing new chemical compounds.
By Susan Young Rojahn on May 23, 2014 WHY IT MATTERS The World health organization predicts that diabetes will be the seventh-leading cause of death by 2030.
and treat diabetes. Researchers have known long that the body carries an enzyme that breaks down insulin inside cells
and helps regulate the body response to sugars process that goes awry in type 2 diabetes.
Genetic studies have shown that people with type 2 diabetes are more likely to have mutations in the gene that encodes a protein called insulin-degrading enzyme, or IDE.
Patients with type 2 diabetes either have an insufficient amount of insulin in their blood
Researchers have speculated for decades that a drug that could inhibit IDE might help some type 2 diabetes patients.
which make up the majority of medicines, are compounds far smaller than less common biological medicines like antibodies.
They are developed using libraries of thousands or millions of known chemical substances. Each compound is screened to see
or other protein known to be involved in a disease. Pharmaceutical companies may use robotics to test many chemical reactions in parallel.
The newly identified IDE inhibitor could be the starting point for developing a powerful new drug for type 2 diabetes.
#Nerve-Stimulating Implant Could Lower Blood pressure An implantable device that reduces blood pressure by stimulating a nerve in the neck could someday be an alternative to drugs for controlling hypertension.
The device is one of the latest efforts to use a nerve-stimulating implant to treat a medical condition.
Such implants might offer new hope to those with extreme hypertension. Up to 30 percent of people with high blood pressure cannot be treated fully with medication
The researchers tested their implant in five adult rats and found that a certain stimulation pattern could reduce the rodents blood pressure by 40 percent without any major side effects.
Plachta says the procedure for implanting the device in humans would be similar to one used in an existing technique that uses vagal-nerve stimulation to treat epilepsy.
which a surgeon would gently wrap the electrodes around the nerve. The device would then be connected to a capsule containing the pulse generator
The whole surgery should take an hour and a half or less says Plachta. The president-elect of the American Society of Hypertension John Bisognano says the work is an impressive and promising application of recent advances in miniaturized electronics and microsurgery.
Bisognano a cardiologist who runs a resistant-hypertension clinic at the University of Rochester Medical center in New york knows well the need for more treatment options.
He says all his patients are on several blood pressure medications and some find that side effects make the drug regimens difficult to maintain.
which means they are at high risk for stroke heart failure and kidney failure he says. Implanted electrical devices that control bodily functions have been used for many years.
but electrical devices are used also to control Parkinson s disease and experimentally some psychiatric conditions (see Brain Pacemakers
and Brain Implants Can Rest Misfiring Circuits). They may be helpful even for such unlikely conditions as bladder dysfunction
and rheumatoid arthritis (see Implanted Device Controls Rheumatoid arthritis). Kristoffer Famm vice president of bioelectronics research and development at Glaxosmithkline coauthored a paper last year on the emergence of the field that he and his academic colleagues call electroceuticals.
Bisognano has reduced successfully blood pressure with experimental implants that stimulate the carotid artery directly an entirely different design from the implant developed by the German group.
Whereas drugs cannot adapt to patient activities an intelligent implant can he says which could offer a way to treat hypertension on demand d
In medical examinersoffices around the United states alone, some 25,000 unidentified human skulls, many of homicide victims, await identification.
Haptic styluses and similar hardware have been used for years for niche applications and for high-end 3-D design and medical trainingor example,
#Implant Lets Patients Regrow Lost Leg Muscle Five people who suffered serious leg injuries have been able to regrow muscle tissue in their legs thanks to a new regenerative medicine treatment.
The new treatment requires intensive surgery to remove scar tissue, after which a biological scaffold is sutured in.
Within two days, the patients began an intensive physical therapy regimen that helps direct the development of stem cells in the body that are drawn to the implant.
Once the stem cells reach the implant, they start making new muscle tissue. The aggressive physical therapy is demanding but critical
two of these injuries were the result of IED blasts. The other two participants were injured in skiing accidents.
Each injury had taken between 60 and 90 percent of thigh muscle or lower leg muscles,
and the participants had undergone already multiple surgeries and physical therapy to try to repair their damaged limbs. rankly,
Although the body has a natural ability to regenerate some muscle after injury, extreme trauma can create gaps that are too large for normal processes to fill,
Such injuries which can be caused by motorcycle accidents, bomb blasts, and more, lead to debilitating condition with limited treatment options, says Andrés García,
The new treatment, described in Science Translational Medicine on Wednesday, is imple yet with significant translational potential,
Biopsies taken six to eight months after the procedure indicated that at least some muscle tissue grew in all five patients
The material is used widely as a passive structural support for abdominal wall hernias, breast reconstruction, and chest wall defects.
As the scaffold starts to break down over several months, it releases biochemical signals that attract the body stem cells to the implant.
The researchers have started treating patients with upper body injuries, and are seeing similar results n
#Cochlear Implant Also Uses Gene therapy to Improve Hearing More than 300,000 people worldwide have cochlear implants.
Cochlear implants use up to 22 platinum electrodes to stimulate the auditory nerve; the devices make a tremendous difference for people
but they restore only a fraction of normal hearing. ochlear implants are very effective for picking up speech,
and dynamics, says Gary Housley, a neuroscientist at the University of New south wales in Sydney, Australia, who led development of the new implant.
So there a physical gap between these atrophied neurons and the electrodes in the cochlear implant.
distributed electrodes of the cochlear implant could be used to achieve the effect. Housley group used deafened guinea pigs
During surgery to place the cochlear implant, they injected the cochlea with a neurotrophin gene vector.
Once the implant was placed, they applied an electroporation voltage using the electrodes. The process, which took only a few seconds during surgery,
resulted in nerve regeneration in the animals. And weeks after implantation, the nerves of treated animals showed stronger responses to signals from the implant,
which suggests they are able to hear more. This research is described this week in the journal Science Translational Medicine. learly this worksn a guinea pig
says Lawrence Lustig, director of the Cochlear Implant Center at the University of California, San francisco Medical center.
Lustig group and others have been exploring gene therapy, but they use a virus to deliver the neurotrophin gene.
whether it for deep-brain stimulation in Parkinson disease, or retinal implants for the blind, there is already neural damage,
a major maker of cochlear implants headquartered in Sydney, to test the electrode and gene therapy combination in a clinical trial i
to prevent serious injury to humans (or worse), these robots are normally shut down when anyone enters their workspace.
in fact, a lot of what we know about cancer genetics comes from research on our fungal friends.
creating living factories for medicines, biofuels, and more (see icrobes Can Mass-produce Malaria Drugand iofuel Plant Opens in Brazil.
The report of the first artificial, designer yeast chromosome suggests ways for researchers to produce new chemicals in the microbes
She not being paranoid. Documents leaked last June by former U s. intelligence contractor Edward Snowden revealed a global surveillance operation coördinated by the U s. National security agency and its counterpart in Britain
my first reaction was had that we discovered junk that would be said highly toxic microbiologist Kim Lewis, director of Northeastern Antimicrobial Discovery Center.
or Streptococcus pneumonia survived and showed no signs of toxicity pleasant surprise to Lewis and his colleagues.
That the antibiotic can kill M. tuberculosis s a major breakthrough because it is virtually certain to be effective for the multi-resistant strains that are now all but impossible to treat,
said Richard Novick, a microbiologist at New york University Langone Medical center who was involved not in the work.
Although further studies are needed before the antibiotic can be tested in humans animal efficacy models are often predictive of a drug effects in humans,
said Gerard Wright, director of the Institute for Infectious disease Research at Mcmaster University in Hamilton, Canada,
drug like this must be reserved for serious diseases and not given to general practitioners to spread around like aspirin
#One-jab universal flu shot in offing MELBOURNE: Scientists have uncovered how human immune cells remember previously encountered strains of influenza,
a discovery that may pave the way for a single universal flu shot to immunize people for their entire lives.
and nobody had immunity. Thankfully, we did manage to contain the virus but we knew we had come face-to-face with a potential pandemic that could kill millions of people around the world
if the virus became able to spread between humans, "she said.""After collecting samples from infected patients we found that people who couldn't make these T cell flu assassins were dying.
These findings lead to the potential of moving from vaccines for specific influenza strains towards developing a protection,
we're talking about a history-altering event on the Spanish flu scale. As it turns out,
"Our extraordinary breakthrough could lead to the development of a vaccine component that can protect against all new influenza viruses, with the potential for future development of a one-off universal flu vaccine shot,
Experts find proof In a major medical breakthrough, scientists at the National Brain Research Centre (NBRC) have reported clinical evidence supporting the role of a novel biomarker in diagnosing Alzheimer's disease.
Glutathione (GSH), the biomarker, is a natural antioxidant that protects the brain from damage. Researchers claim that those suffering from the disease have reduced GSH as compared to the healthy individuals."
"The conventional methods for diagnosis of Alzheimer's depend mostly on clinical symptoms or biopsy which is an invasive procedure.
However, the new biomarker can be assessed by MRI-like imaging tests. Also, it can help predict the disease much before its onset,
"said Dr Pravat Mandal, a professor at NBRC and associate professor (adjunct) at the John Hopkins University, Maryland, USA.
"Several animal studies conducted at NBRC have showed the utility of this biomarker in diagnosing Alzheimer's disease previously also.
The findings have been accepted by the international journal'Biological Psychiatry'for publication.""A total 130 people0 Alzheimer's patient, 41 patients suffering from mild cognitive impairment and 49 healthy individualsarticipated in the study.
the patients were recruited through referral from neurologists at AIIMS, the researchers said. They claimed GSH estimation in Hippocampi,
a region of the brain, yielded 100%specificity and sensitivity for distinguishing Alzheimer's disease and healthy controls."
"We propose that estimation of GSH affords a crucial noninvasive measure of Alzheimer's disease progression that could
not only provide clinical insight about the disease's pathophysiology but also expedite the drug development process,
Dr Kameshwar Prasad, professor and head of neurology at AIIMS, said the findings are preliminary."
"If it succeeds to become a practical solution for early diagnosis of Alzheimer's. Early identification can help in giving drug therapy to slow the degeneration process
and develop strategies to enhance the patient's living environment, "he said. Alzheimer's is one of the common brain disorders that affects nearly 35 million people worldwide.
By 2050, experts said, about one in 85 individuals over the age of 65 years will suffer from the disease s
#Created: First artificial molecular pump WASHINGTON: Scientists have developed the first man-made molecular pump, which transports key proteins that cells need to function,
#Researchers find new way to treat diabetic blindness WASHINGTON: US researchers said they have found a new way to restore the eyesight in patients who have a blinding eye disease caused by diabetes.
The key is to block a second blood vessel growth protein, along with one that is already well-known,
and preventing diabetic retinopathy, the most common diabetic eye disease, they reported in the US journal Proceedings of the National Academy of Sciences, Xinhua news agency reported.
Diabetic retinopathy occurs when the normal blood vessels in the eye are replaced over time with abnormal,
damaging the light-sensitive retina and causing blindness. Forty to 45 percent of Americans with diabetes have diabetic retinopathy, according to the US National Eye Institute.
Laser-sealing eye blood vessels can save central vision, but this often sacrifices peripheral and night vision, according to the researchers at the Johns hopkins university and the University of Maryland.
But studies have shown that although these drugs slow progression to proliferative diabetic retinopathy, it does not reliably prevent it,
said lead author Akrit Sodhi, an assistant professor of ophthalmology at the Johns hopkins university School of medicine. To find an explanation,
people with diabetes who did not have diabetic retinopathy and people with diabetic retinopathy of varying severity were tested.
While levels of VEGF tended to be higher in those with proliferative diabetic retinopathy some of their fluid had less VEGF than did the healthy participants.
But even the low-VEGF fluid from patients with proliferative diabetic retinopathy stimulated blood vessel growth in lab-grown cells."
"The results suggested to us that although VEFG clearly plays an important role in blood vessel growth,
and angiopoietin-like 4 in fluid from the eyes of people with proliferative diabetic retinopathy, it markedly reduced blood vessel growth in lab-grown cells.
it might be combined with the anti-VEGF drugs to prevent many cases of proliferative diabetic retinopathy.
whether angiopoietin-like 4 might also play a role in other eye diseases, such as macular degeneration,
US researchers said they have found a new way to restore the eyesight in patients who have a blinding eye disease caused by diabetes.
and preventing diabetic retinopathy, the most common diabetic eye disease, they reported in the US journal Proceedings of the National Academy of Sciences, Xinhua news agency reported.
Diabetic retinopathy occurs when the normal blood vessels in the eye are replaced over time with abnormal,
damaging the light-sensitive retina and causing blindness. Forty to 45 percent of Americans with diabetes have diabetic retinopathy, according to the US National Eye Institute.
Laser-sealing eye blood vessels can save central vision, but this often sacrifices peripheral and night vision, according to the researchers at the Johns hopkins university and the University of Maryland.
But studies have shown that although these drugs slow progression to proliferative diabetic retinopathy, it does not reliably prevent it,
said lead author Akrit Sodhi, an assistant professor of ophthalmology at the Johns hopkins university School of medicine. To find an explanation,
people with diabetes who did not have diabetic retinopathy and people with diabetic retinopathy of varying severity were tested.
While levels of VEGF tended to be higher in those with proliferative diabetic retinopathy some of their fluid had less VEGF than did the healthy participants.
But even the low-VEGF fluid from patients with proliferative diabetic retinopathy stimulated blood vessel growth in lab-grown cells."
"The results suggested to us that although VEFG clearly plays an important role in blood vessel growth,
and angiopoietin-like 4 in fluid from the eyes of people with proliferative diabetic retinopathy, it markedly reduced blood vessel growth in lab-grown cells.
it might be combined with the anti-VEGF drugs to prevent many cases of proliferative diabetic retinopathy.
whether angiopoietin-like 4 might also play a role in other eye diseases, such as macular degeneration,
#Machine that unboils eggs now being used to improve cancer treatment A machine that can be used to uncook eggs is now being used to dramatically improve the effectiveness of a cancer treatment.
Using the invention on carboplatin a common cancer treatment drug, used against ovarian and lung cancers has boosted the potency by almost five times.
and this has got applications in chemistry, engineering, biology, medicine, so there's a lot of potential there and that's just for research purposes,
"Raston told ABC News. A machine that can be used to uncook eggs is now being used to dramatically improve the effectiveness of a cancer treatment.
Using the invention on carboplatin a common cancer treatment drug, used against ovarian and lung cancers has boosted the potency by almost five times.
and this has got applications in chemistry, engineering, biology, medicine, so there's a lot of potential there and that's just for research purposes,
#In a first, cold sore virus used to fight cancer cells Scientists have the first proof that a"brand new"way of combating cancer,
Specialists at the NHS Royal Marsden Hospital and the Institute of Cancer Research (ICR) confirmed that melanoma skin cancer patients treated with a modified herpes virus (the virus that causes cold sores) had improved survival-a world first.
inoperable malignant melanoma, those treated with the virus therapy-known as T-VEC-at an earlier stage survived, on average,
randomised trial of a so-called oncolytic virus to show success. Cancer scientists predict it will be the first of many in the coming years-adding a new weapon to our arsenal of cancer treatments.
Other forms of immunotherapy-the stimulation of the body's own immune system to fight cancer-using antibodies rather viruses,
Viral immunotherapies are also being investigated for use against advanced head and neck cancers, bladder cancers and liver cancers.
Kevin Harrington, UK trial leader and professor of biological cancer therapies at the ICR and an honorary consultant at the Royal Marsden, said he hoped the treatment could be available for routine use within a year in many countries
"We hope this is the first of a wave of indications for these sorts of cancer fighting agents that we will see coming through in the next decade or so."
and kill human cells that can make them such promising cancer treatments.""The study, which is published in the Journal of Clinical Oncology, included 436 patients, all of
whom had aggressive, inoperable malignant melanoma. More than 16 per cent of patients were responding to treatment after six months,
Alan Melcher, professor of clinical oncology and biotherapy at the University of Leeds, and an expert in oncolytic viruses, said the field had accelerated quickly in recent years."
is that they work by stimulating an immune response against cancer, "he said.""The field has moved very quickly clinically.
"Dr Hayley Frend, science information manager at Cancer Research UK, said the potential for viruses in future cancer treatments was"exciting"."
Melanoma is the fifth most common cancer in the UK, and is becoming more widespread
if the cancer-indicated by the appearance of a new mole on the skin-is caught early.
and 2, 000 people still die from melanoma in the UK every year. Scientists have the first proof that a"brand new"way of combating cancer,
using genetically modified viruses to attack tumour cells, can benefit patients, paving the way for a"wave"of new%potential treatments over the next decade.
Specialists at the NHS Royal Marsden Hospital and the Institute of Cancer Research (ICR) confirmed that melanoma skin cancer patients treated with a modified herpes virus (the virus that causes cold sores) had improved survival-a world first.
those treated with the virus therapy-known as T-VEC-at an earlier stage survived, on average,
randomised trial of a so-called oncolytic virus to show success. Cancer scientists predict it will be the first of many in the coming years-adding a new weapon to our arsenal of cancer treatments.
Other forms of immunotherapy-the stimulation of the body's own immune system to fight cancer-using antibodies rather viruses,
Viral immunotherapies are also being investigated for use against advanced head and neck cancers, bladder cancers and liver cancers.
Kevin Harrington, UK trial leader and professor of biological cancer therapies at the ICR and an honorary consultant at the Royal Marsden, said he hoped the treatment could be available for routine use within a year in many countries
"We hope this is the first of a wave of indications for these sorts of cancer fighting agents that we will see coming through in the next decade or so."
and kill human cells that can make them such promising cancer treatments.""The study, which is published in the Journal of Clinical Oncology, included 436 patients, all of
whom had aggressive, inoperable malignant melanoma. More than 16 per cent of patients were responding to treatment after six months,
Alan Melcher, professor of clinical oncology and biotherapy at the University of Leeds, and an expert in oncolytic viruses, said the field had accelerated quickly in recent years."
is that they work by stimulating an immune response against cancer, "he said.""The field has moved very quickly clinically.
"Dr Hayley Frend, science information manager at Cancer Research UK, said the potential for viruses in future cancer treatments was"exciting"."
Melanoma is the fifth most common cancer in the UK, and is becoming more widespread
if the cancer-indicated by the appearance of a new mole on the skin-is caught early.
and 2, 000 people still die from melanoma in the UK every year r
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