Showing posts with label discover. Show all posts
Showing posts with label discover. Show all posts

Thursday, March 13, 2014

Farewell to Discover

It has been just over a year since I posted Lighting the Match, the first entry in this venture called Fire in the Mind. During that time I’ve written about a variety of subjects from fluoride paranoia to the mystical mathematics of rock and roll. Some of my favorite posts were about Oliver Sacks and his idiot-savant prodigies, the beguiling psychology of cancer clusters, Rosalind Franklin’s missed opportunity to discover the double helix, the infinite obsessions of David Foster Wallace, and Jhumpa Lahiri and the magic of perfectly chosen words. There was also a dispatch about Horace Freeland Judson, author of the best science book ever written. His daughter, Olivia Judson, has been writing a moving series in the Times about cleaning out her famly’s old house in Baltimore. (Be especially sure to read part 5, A Piece of DNA, in which she comes across part of Watson and Crick’s famous wire and sheet metal model.)

Toward the end of my run, I wrote mostly about the mysteries of cancer, the topic of my most recent book, with a side trip into the peculiarities of one of the most brilliant people alive, Murray Gell-Mann, the reluctant subject of my biography, Strange Beauty. He is 84.

Now it is time to move on. In January I began a monthly column, Raw Data, for the New York Times. It will appear every third Tuesday in the science section, online and in print, and sometimes in between. The first two installments were about irreproducible experiments, confirmation bias, and the role of subjectivity in science. But as the column continues, it will range over as wide a ground as “Fire in the Mind,” which ends now with this post. For the time being, the old entries will stay here, though I may eventually move them to my website, talaya.net.

I was an early adopter of  the Internet, hand-coding my own web pages on a Unix command line with an editor called pico. (The real hardcores use vi.) I accessed the web by telnetting to a server at CERN and later with a barebones browser – text only – called lynx. On equal footing back then with WWW were WAIS (wide area information server) and Gopher (from the University of Minnesota). With the invention of Mosaic, the first graphical web browser, they have become all but obsolete.

Things have gotten better and worse since then. There were no ads or “search engine optimization” and it was years before I received my first spam, reading it with an email program called pine. (I also received around that time an email invitation from Steve Case,  founder of AOL, to buy 1,000 shares of his company for $10 each. Knowing that AOL was not the future, I declined. I was right but I could have become wealthy in the short run.) I still like to play around with Unix, and I run my own domain and email server on an old Mac Pro in my office. But nothing beats ink on paper.

I’ve enjoyed being at Discover and I thank the editors, especially Tasha Eichenseher, who has moved on to other ventures, and Siri Carpenter, who is rising rapidly through the ranks. Many other good people remain, and more are on their way, including (from my hometown of Santa Fe) April Reese. Last I heard via Twitter, she and a friend were approaching Discover’s home office from somewhere in Nebraska.

I hope some of you will become readers of Raw Data and continue to follow me @byGeorgeJohnson.

photo by Kerry Sherck photo by Kerry Sherck

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Thursday, September 12, 2013

Scientists discover key to normal memory lapses in seniors

By Sharon Begley

NEW YORK | Wed Aug 28, 2013 2:24pm EDT

NEW YORK (Reuters) - Scientists have good news for all the older adults who occasionally forget why they walked into a room - and panic that they are getting Alzheimer's disease.

Not only is age-related memory loss a syndrome in its own right and completely unrelated to that dread disease, but unlike Alzheimer's it may be reversible or even preventable, researchers led by a Nobel laureate said in a study published on Wednesday.

Using human brains that had been donated to science as well as the brains of lab mice, the study for the first time pinpointed the molecular defects that cause cognitive aging.

In an unusual ray of hope for a field that has had almost nothing to offer older adults whose memory is failing, the study's authors conclude that drugs, foods or even behaviors might be identified that affect those molecular mechanisms, helping to restore memory.

Any such interventions would represent a significant advance over the paltry offerings science has come up with so far to prevent memory decline, such as advice to keep cognitively active and healthy - which helps some people, but not all, and has only a flimsy scientific foundation. By identifying the "where did I park the car?" molecule, the discovery could also kick-start the mostly moribund efforts to develop drugs to slow or roll back the memory lapses that accompany normal aging.

"This is a lovely set of studies," said Molly Wagster of the National Institute on Aging, an expert on normal age-related memory decline who was not involved in the new study. "They provide clues to the underlying mechanism of age-related memory decline and will, hopefully, move us down the road toward targeted therapeutics."

About 40 percent of Americans age 85 and older say they experience some memory loss, a 2009 survey by the Pew Research Center found, as did 27 percent of those 75 to 84 and 20 percent of those ages 65 to 74.

BRAIN BANK

The researchers began with eight brains from the New York Brain Bank at Columbia University donated by people aged 33 to 88 who were free of brain disease when they died. They extracted two structures in the hippocampus, a vital cog in the brain's memory machinery: the dentate gyrus, a boomerang-shaped region whose function declines with age but is not affected by Alzheimer's, and the entorhinal cortex, which is largely unaffected by aging but is where Alzheimer's first takes hold, killing neurons.

The scientists then measured which genes had been active in each structure, and found one suspicious difference: 17 genes in the dentate gyrus became more active, or less, as the age of the brain increased.

The most significant change was that the gene for a protein called RbAp48 had essentially retired: The gene's activity tailed off dramatically the older a brain got. As a result, old brains had about half the RbAp48 of young brains, the scientists report online in the journal Science Translational Medicine.

The scientists then sampled 10 more healthy human brains, ranging from 41 to 89 years at the time of death. Once again, the amount of RbAp48 protein declined with age in the dentate gyrus. They next confirmed that RbAp48 protein was also less abundant in the dentate gyrus of old mice compared to young ones.

For the final step, the scientists had to nail down whether the missing protein caused age-related memory loss. They genetically engineered mice whose RbAp48 genes were disabled. Result: The young mice had memories as poor as animals four times their age (the mouse equivalent of late middle age), and they had terrible trouble navigating a water maze or differentiating objects they had seen before from novel ones.

Crucially, the scientists also did the reverse experiment, engineering mice so their brains had extra doses of RbAp48. The mice's memories returned to the flower of youth.

"With RbAp48, we were able to reverse age-related memory loss in the mice," said Columbia's Dr Eric Kandel, who shared the 2000 Nobel Prize in medicine for discoveries of the molecular basis of memory and led the research. "Unlike in Alzheimer's, there is no significant cell death in age-related memory loss, which gives us hope it can be prevented or reversed."

Exactly how RbAp48 does that is not clear. The protein acts as a sort of genetic master key: By causing chromosomes to loosen their hold on the molecular spool they are wound around like thread, it allows genes to be turned on. Among the activated genes, Kandel explained, are those involved in forming memories.

The emerging picture is that levels of RbAp48 decline with age, allowing chromosomes to maintain a death grip on their spools. Memory genes remain dormant, and you can't remember that you promised your spouse you would make dinner.

The researchers plan to see what social and dietary factors might boost RbAp48 in mice, said Kandel, who will be 84 in November. Pharmaceuticals, nutraceuticals, physical and cognitive exercise are all candidates, said Columbia's Dr Scott Small, co-senior author of the study.

Testing such interventions in mice should be more useful to humans than tests of drugs for Alzheimer's, he said. RbAp48 "is different," Small said. "Alzheimer's does not occur naturally in the mouse. Here, we've caused age-related memory loss in the mouse, and we've shown it to be relevant to human aging."

(Reporting by Sharon Begley; Editing by Julie Steenhuysen and Prudence Crowther)


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Tuesday, April 23, 2013

Discover JPL Brochure Receives Communicator Awards

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$(document).ready(function(){$('.star-rating').rating({callback: function(value, link){ $.post("../../", {fuseaction: 'starrating.submitrating', starratingid:$("#starratingid").val(), objecttype:$("#objecttype").val(), objectid:$("#objectid").val(),starrating:value}, function(obj) { $('.star-rating').rating('readOnly',true); var newobj = eval('(' + obj + ')'); $('#starratingleftcontainer').html('Average Rating: ' + newobj.ratio + ' / 5 ('+ newobj.ratinghits +' ratings)'); $('#starratingid').val(newobj.starratingid); });}});$("#starratinghelpicon").hover(function() {$("#starratinghelptextcontainer").animate({opacity: "show"}, "slow");}, function() {$("#starratinghelptextcontainer").animate({opacity: "hide"}, "fast");});});Average Rating: 5 / 5 (4 ratings) Discover JPL Brochure Receives Communicator AwardsDiscover JPL Brochure Receives Communicator Awards

The Discover JPL brochure, developed in partnership with JPL's University Research Affairs office, is the recent recipient of several Communicator Awards that recognize excellence in communications.

The International Academy of Visual Arts has recently awarded several Communicator Awards to the team responsible for creating the Discover JPL brochure at NASA’s Jet Propulsion Laboratory, Pasadena, Calif. The Communicator Awards are given out annually to recognize excellence in marketing and communications.

Discover JPL took home distinctions in the Print Category, for Non-Profit Brochure, Recruitment Brochure, and Overall Brochure Design. The brochure was designed by CMg Design Inc., under the direction of JPL’s University Research Affairs Office.

The Discover JPL brochure gives an inside look at JPL's collaborative relationships with the academic community. These partnerships provide accelerated innovation for NASA’s missions and the discovery of new science and technology opportunities. Highlighted in this brochure are features about how students have contributed to various science, engineering and technology projects at JPL.

To view the Discover JPL brochure, visit: http://scienceandtechnology.jpl.nasa.gov/files/JPL_Student_Research_Brochure_2010.pdf


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