Interview with geneticist George Church as part of the Experience series.
Visiting professor Sasha Kimel examined whether information about genetic links can influence groups in conflict.
Scientists identify a molecular key that helps cells maintain identity and prevents the conversion of adult cells into induced pluripotent stem cells — a process that would require a cell to “forget” its identity before assuming a new one.
Today’s discoveries in DNA technology are as exciting as another era’s moon missions, opening avenues of scientific inquiry and invigorating even longstanding fields, speakers at a Radcliffe science symposium on DNA said.
A team of scientists has engineered a form of the genome-editing protein Cas9 that can be controlled by a small molecule and offers improved DNA specificity.
New research illuminates the mixing with Neanderthals in early human prehistory, narrowing the window of time when they crossbred to between 50,000 and 60,000 years ago.
Harvard researchers working at the Broad Institute of MIT and Harvard have uncovered nine rare genetic mutations that dramatically increase the risk of developing type 2 diabetes. The discovery of the mutations highlights the dizzying genetic diversity of a disease rapidly spreading around the world.
Using genetic tools to implant genes that produce fluorescent proteins in the DNA of transparent C. elegans worms, Harvard scientists have been able to shed light on neuron-specific “alternative splicing,” a process that allows a single gene to produce many different proteins.
Harvard Stem Cell Institute scientists collaborating with researchers at the University of Pennsylvania have developed a “genome-editing” approach for permanently reducing cholesterol levels in mice through a single injection, a development with the potential to reduce the risk of heart attacks in humans by 40 to 90 percent.
A large international consortium of researchers has produced the first comprehensive, detailed map of the way genes work across the major cells and tissues ...
Scientists at the Wyss Institute for Biologically Inspired Engineering at Harvard University have discovered a way to build self-assembling cages made of DNA. The cages are the largest stand-alone DNA structures made to date, and one day may be able to deliver drugs or house tiny bioreactors or photonic devices inside the human body.
Research by Harvard Stem Cell Institute scientists shows that much lincRNA, which had been generally believed useless, plays an important role in the genome.
The ACLU’s lead attorney and other participants in the Supreme Court case that overturned the common practice of patenting human genes discussed the ramifications in an event at the Science Center.
Experts in child health gathered at Harvard Medical School on Tuesday for a symposium on how genome biology is changing children’s health.
With a new flu virus appearing in China in April and a new SARS-like respiratory ailment appearing in the Middle East, the Gazette sat down with Harvard epidemiologist Marc Lipsitch to talk about the upcoming flu season.
Harvard researchers recently developed the most detailed “specificity profile” for Cas9 — a “machine” made of protein and RNA that can be programmed to target specific DNA sequences and to precisely cut, paste, and turn on or turn off genes. Future researchers will use the data when developing genetic tools and therapies.
A team of researchers at the Wyss Institute has found a way to self-assemble complex structures out of gel “bricks” smaller than a grain of salt. The new method could help solve one of the major challenges in tissue engineering.
Scientists may soon be able to turn to one of the most powerful forces in biology — evolution — to help in their quest to develop new synthetic polymers.
In a new paper, Harvard researchers show that changes in coat color in mice are the result not of a single mutation, but of many mutations, all in a single gene. The results start to answer one of the fundamental questions about evolution: Does it proceed by huge leaps — single mutations that result in dramatic changes in an organism — or is it the result of many smaller changes over time?
For decades, scientists wondered whether there was some subtle difference between parts of the genetic code that, while different, appear to encode the same amino acid. Harvard researchers now have the answer.
Scientists at Harvard have pioneered a breakthrough technique that can reproduce an individual’s entire genome from a single cell. The development could revolutionize everything from cancer treatment, by allowing doctors to obtain a genetic fingerprint of a person’s cancer early in treatment, to prenatal testing.
Geneticist Elaine Ostrander runs a comparative-genomics lab that examines dog DNA to understand better the traits that might aid understanding of human diseases.
Most of the DNA alterations that are tied to disease do not alter protein-coding genes, but rather the “switches” that control them. Characterizing these switches is one of many goals of the Encyclopedia of DNA Elements (ENCODE) project.
Research led by scientists at Harvard and University College London has shown that Native Americans arrived in three waves of migration, not one, as is commonly held and that at least one group returned home to Asia.
Research is uncovering the genetic roots of aging, peeling back the once common understanding that creatures simply “wore out” as they aged, and slowly revealing the mechanisms that control a process determined by our genes and that proceeds at different speeds for different species.
Researchers at Harvard’s Wyss Institute for Biologically Inspired Engineering have figured out how to use short lengths of DNA as physical, rather than genetic, building blocks, creating letters and other shapes from the molecules in a proof of design that could one day lead to the creation of structures that, among other things, deliver drugs to disease sites.
Anne Wojcicki, chief executive officer and co-founder of 23andMe, talked about growth in personal genomics in an event sponsored by the Program on Science, Technology and Society.
Scientists from Harvard-affiliated Brigham and Women's Hospital and Dana-Farber Cancer Institute and their colleagues have found a genetic marker that predicts which aggressive “triple-negative” breast cancers and certain ovarian cancers are likely to respond to platinum-based chemotherapies.
A new imaging technique, developed by Erez Lieberman-Aiden, a Junior Fellow of the Society of Fellows, is giving scientists their first three-dimensional view of the human genome, one that is already shedding new light on a number of what Liberman-Aiden calls the “central mysteries of biology.”
As reported in the online version of Nature Structural & Molecular Biology on Feb. 5, researchers have produced 3-D images of the protein system that works to repair DNA. The images reveal that the proteins can actually alter their shape in what amounts to a genetic “pat-down,” or a way for the mechanism to identify areas of the genetic code that need repair.
Researchers at the Wyss Institute for Biologically Inspired Engineering at Harvard University have developed a robotic device made from DNA that could potentially seek out specific cell targets within a complex mixture of cell types and deliver important molecular instructions, such as telling cancer cells to self-destruct or programming immune responses.
As science wrestles with the problem of how life arose on Earth, hindsight shows that seemingly intractable obstacles can have simple, even elegant solutions, said Nobel laureate Jack Szostak.
Researchers at Harvard Medical School and Children’s Hospital Boston have retraced the evolution of an unusual bacterial infection as it spread among cystic fibrosis patients by sequencing scores of samples collected during the outbreak, since contained.
Researchers have decoded the genome of an unlikely ally in the fight against cancer and aging, the naked mole rat, to find clues on why it resists the disease and lives 10 times as long as ordinary mice.
Scientists at Harvard-afilliated Dana-Farber Cancer Institute and the Broad Institute have found strikingly high levels of a bacterium in colorectal cancers, a sign that it might contribute to the disease and potentially be a key to diagnosing, preventing, and treating it.
Looking at large samples, an international consortium — that included involvement by scientists at the Broad Institute of Harvard and MIT and Harvard-affiliated Massachusetts General Hospital (MGH) — has identified 10 genetic risk factors that contribute to either schizophrenia or bipolar disorder and discovered strong evidence for three genes being implicated in both diseases.
An international team of researchers studying DNA patterns from modern and archaic humans has found that the Denisovans, a recently discovered hominin group, contributed genes to several populations in Asia and that modern humans settled Asia in more than one migration.
Scientists at Harvard-affiliated Dana-Farber Cancer Institute have successfully disrupted the function of a cancer gene involved in the formation of most human tumors by tampering with the gene’s “on” switch and growth signals, rather than targeting the gene itself.
A consortium led by scientists at the University of Oxford and Harvard Medical School has constructed the world’s most detailed genetic map, built from data from 30,000 African-Americans. The researchers assert that this is the most accurate and highest resolution genetic map yet.
Harvard Medical School researchers have traced the influence of genes from sub-Saharan Africa in European, Middle Eastern, and Jewish populations, quantifying the intermingling that occurred over many generations.
During a trip to the Museum of Science, Harvard College Dean Evelynn M. Hammonds and students from her freshman seminar revisited many of the issues they explored in her fall class.
RNA plays a critical role in directing the creation of proteins, but there is more to the life of an RNA molecule than simply carrying DNA’s message.
Two panel discussions, organized by the Harvard School of Engineering and Applied Sciences, examined the “promise and perils” of creating digital repositories of genetic records and considered the policy implications of an individual’s right to access, control, and interpret his or her own genetic data.
Harvard scientists have unveiled the most comprehensive picture to date of the full genetic blueprint of multiple myeloma, a form of blood cancer.
On a day when Harvard celebrated the accomplishments of the Human Genome Project, the Radcliffe Institute hosted a scientist whose work focuses not just on DNA, but on the mechanisms that control its expression.
Harvard President Drew Faust hosted a panel discussion on the legacy of the Human Genome Project Feb. 22 at Sanders Theatre.
The field of genomics, after revolutionizing crime fighting through DNA testing, is likely to shake the political landscape, says Jennifer Hochschild, who is researching its implications in Washington, D.C.
To mark the 10th anniversary of the publication of the Human Genome Map, Harvard President Drew Faust will host a panel discussion on the project next week (Feb. 22) in Sanders Theatre.
Harvard researchers at the Dana-Farber Cancer Institute have identified the root molecular cause of a variety of ills brought on by advanced age, including waning energy, failure of the heart and other organs, and metabolic disorder.
By comparing the DNA of modern elephants from Africa and Asia to DNA extracted from two extinct species, the woolly mammoth and the mastodon, researchers have concluded that Africa has two — not one — species of elephant. Now that we know the forest and savanna elephants are two very different animals, the forest elephant should become a bigger priority for conservation purposes.