Purdue Univ. researchers have identified an important enzyme pathway that helps prevent new cells from receiving too many or too few chromosomes, a condition that has been directly linked to cancer and other diseases. The team found that near the end of cell division, the enzyme Cdc14 activates Yen1, an enzyme that ensures any breaks in DNA are fully repaired before the parent cell distributes copies of the genome to daughter cells.
It's a familiar trope in science fiction: In enemy territory, activate your cloaking device. And...
Our DNA is under constant attack from many sources. Fortunately, cells have several major DNA...
Using nanodot technology, Lawrence Berkeley National Laboratory researchers have demonstrated...
Huntington's disease is a grim diagnosis. A hereditary disorder with debilitating physical and cognitive symptoms, the disease usually robs adult patients of their ability to walk, balance and speak. More than 15 years ago, researchers revealed the disorder's likely cause—an abnormal version of the protein huntingtin; however, the mutant protein's mechanism is poorly understood, and the disease remains untreatable.
A drug under clinical trials to treat tuberculosis could be the basis for a class of broad-spectrum drugs that act against various bacteria, fungal infections and parasites, yet evade resistance, according to a study by Univ. of Illinois chemists and collaborators. The team determined the different ways the drug SQ109 attacks the tuberculosis bacterium and how the drug can be tweaked to target other pathogens from yeast to malaria.
From far away, the top of a leaf looks like one seamless surface; however, up close, that smooth exterior is actually made up of a patchwork of cells in a variety of shapes and sizes. Interested in how these cells individually take on their own unique forms, a Caltech team sought to pinpoint the shape-controlling factors in pavement cells, which are puzzle-piece-shaped epithelial cells found on the leaves of flowering plants.
A type of single-cell green algae called Chlamydomonas reinhardtii is a leading subject for photosynthesis research, but few tools are available for characterizing the functions of its genes. A team including Carnegie Institution's Martin Jonikas has developed a highly sophisticated tool that will transform the work of plant geneticists by making large-scale genetic characterization of Chlamydomonas mutants possible for the first time.
Driven by rapid growth in forensics, biotechnology, disease diagnostics and environmental regulations, chromatography systems have become a laboratory staple. Used for the separation of complex mixtures, detection of illicit drugs and the production of pharmaceuticals, the biotechnology and pharmaceutical industries are the prime users of chromatography techniques.
In a new study, researchers from North Carolina State Univ., UNC-Chapel Hill and other institutions have taken the first steps toward creating a roadmap that may help scientists narrow down the genetic cause of numerous diseases. Their work also sheds new light on how heredity and environment can affect gene expression.
Builders and factory workers know that getting a job done right requires precision and specialized tools. The same is true when you’re building antibiotic compounds at the molecular level. New findings from North Carolina State Univ. may turn an enzyme that acts as a specialized “wrench” in antibiotic assembly into a set of wrenches that will allow for greater customization.
T-cells use a complex process to recognize foreign pathogens and diseased cells. In a paper published in Cell, researchers add a new level of understanding to that process by describing how the T-cell receptors use mechanical contact—the forces involved in their binding to the antigens—to make decisions about whether or not the cells they encounter are threats.
Lots of apps claim they can help you fight jet lag. Now Michigan researchers say mathematical formulas suggest it's possible to adjust to new time zones a bit faster than previously thought, and they created their own free app to help. Doctors have long said exposure to light is key. But how much, and when?
Univ. of Texas at Arlington and Texas Health Arlington Memorial Hospital are investigating whether bone grown from the body’s own stem cells can replace traditional types of bone grafting. The process, which has been successful in previous lab experiments, uses biodegradable polymer scaffolding material and bone morphogenetic protein, or BMP, which was inserted into the abdomen of mice to attract stem cells that in turn produced bone.
By attaching short sequences of single-stranded DNA to nanoscale building blocks, researchers can design structures that can effectively build themselves. The building blocks that are meant to connect have complementary DNA sequences on their surfaces, ensuring only the correct pieces bind together as they jostle into one another while suspended in a test tube.
Synthetic collagen invented at Rice Univ. may help wounds heal by directing the natural clotting of blood. The material, KOD, mimics natural collagen, a fibrous protein that binds cells together into organs and tissues. It could improve upon commercial sponges or therapies based on naturally derived porcine or bovine-derived collagen now used to aid healing during or after surgery.
The Japanese scientist accused of falsifying data in a widely heralded stem-cell research paper said Wednesday the results are valid despite mistakes in their presentation. Haruko Obokata, 30, struggled to maintain her composure during a televised news conference packed with hundreds of reporters, but insisted she did not tamper with the data to fabricate results.
Researchers have discovered that the so-called HOPE method allows tissue samples to be treated such that they do not only meet the requirements of clinical histology, but can still be characterized later on by modern methods of proteomics, a technique that analyzes all proteins at once. This differs from the traditional formalin-based approach that cross-links protein molecules.
Data about DNA differences, gene expression or methylation can each tell epidemiologists something about the link between genomics and disease. A new statistical model that can integrate all those sources provides a markedly improved analysis, according to two new papers.
Under the microscope, they glow like streetlights, forming tidy rows that follow the striations of muscle tissue. They are mitochondria—the powerhouses of cells—and researchers at the Univ. of Virginia School of Medicine have created a method to illuminate and understand them in living creatures like never before.
Synthetic genetic circuitry created by researchers at Rice Univ. is helping them see, for the first time, how to regulate cell mechanisms that degrade the misfolded proteins implicated in Parkinson’s, Huntington’s and other diseases. The Rice team has designed a sophisticated circuit that signals increases in the degradation of proteins by the cell’s ubiquitin proteasome system (UPS).
Chances are you've heard of mapping genes to diagnose rare diseases, predict your risk of cancer and tell your ancestry. But to uncover food poisonings? The nation's disease detectives are beginning a program to try to outsmart outbreaks by routinely decoding the DNA of potentially deadly bacteria and viruses.
Researchers have reported they can generate human motor neurons from stem cells much more quickly and efficiently than previous methods allowed. The new method involves adding critical signaling molecules to precursor cells a few days earlier than previous methods specified. This increases the proportion of healthy motor neurons derived from stem cells (from 30 to 70%) and cuts in half the time required to do so.
As the Earth’s human population marches toward 9 billion, the need for hardy new varieties of grain crops has never been greater. It won’t be enough to yield record harvests under perfect conditions; new grains must also be able to handle stress from climate changes. Researchers in Michigan have recently identified a set of genes that could be key to the development of the next generation of super rice.
Using a new gene-editing system based on bacterial proteins, Massachusetts Institute of Technology researchers have cured mice of a rare liver disorder caused by a single genetic mutation. The findings offer the first evidence that this gene-editing technique, known as CRISPR, can reverse disease symptoms in living animals.
Long before next-generation sequencing technology appeared, clinicians have been taking family histories by jotting down pedigrees: hand-drawn diagrams recording how diseases may recur across generations. Now healthcare providers can create those diagrams digitally on an iPad screen with a few finger taps, during a face-to-face encounter with an individual and his or her family.
New findings challenge the prevailing wisdom about how our body clocks are organized, and suggest that interactions among neurons that govern circadian rhythms are more complex than originally thought. A Univ. of Michigan team looked at the circadian clock neuron network in fruit flies, which is functionally similar to that of mammals, but at only 150 clock neurons is much simpler.
Now that the human genome is sequenced, researchers are focusing on the study of the proteome, which is the protein content of an organism, tissue or cell. Bioanalytical chemists at Univ. of Notre Dame have successfully tracked the changing patterns of protein expression during early development of African clawed frog embryos, producing the largest data set on developmental proteomics for any organism.
A new understanding of proteins at the nexus of a cell’s decision to survive or die has implications for researchers who study cancer and age-related diseases, according to biophysicists at the Rice Univ.-based Center for Theoretical Biological Physics. Experiments and computer analysis of two key proteins revealed a previously unknown binding interface that could be addressed by medication.
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