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Scientists work with animal models to better understand type 2 diabetes to treat the disease. They have developed specialized animal models that mimic the condition.  One line of mice, known as KK mice, develop obesity and glucose intolerance that lead to type 2 diabetes. Another rodent model, the Zucker diabetic fatty rat, is bred to be a precise model of human type 2 diabetes.

A handful of scientists around the United States are trying to do something that some people find disturbing: make embryos that are part human, part animal. The researchers hope these embryos, known as chimeras, could eventually help save the lives of people with a wide range of diseases.

Lyme disease, Ebola and malaria all developed in animals before making the leap to infect humans. Predicting when such a 'zoonotic' disease will spark an outbreak remains difficult, but a new study suggests that artificial intelligence could give these efforts a boost. A computer model that incorporates machine learning can pinpoint, with 90% accuracy, rodent species that are known to harbour pathogens that can spread to humans, researchers report this week in the Proceedings of the National Academy of Sciences1. The model also identified more than 150 species that are likely to be disease reservoirs but have yet to be confirmed as such.

A dynamic 3D computer animated video takes you "inside" for a close-up look at how we're made. Watch as the mysteries of the Human Genome are literally "unraveled." 3D modeling and animation created by Bill Baker, Bakedmedia, Inc. and Mike Fisher for the National Human Genome Research Institute.

Recently, in an article in the New Republic, 'The Animals That Can Save Your Life', journalist Emma Young introduces readers to the emerging science of training animals to detect things humans cannot.

Hear from some of the country's leading scientists and medical experts who talk about why animal research is critical for medical progress and the advancement of both human and animal health.

Sure, we know insufficient serotonin levels get a bad rap when it comes to depression, but that's like blaming one person in a full-scale riot. Depression isn't caused by only one factor. In fact, study co-author Elyse Aurbach says we're probably not getting to the core of why people are depressed because "the brain is immensely complex." In this study, the research team conducted eight experiments (four on animal brains, four on brains of the deceased human kind) of varying sample sizes - from 20 to 90 brains in each - and found that the brains of deceased humans who'd been depressed had increased levels of hippocampal FGF9 and that live animals with increased FGF9 levels demonstrated depressive, anxious behavior. "This is not just a correlation," study leader Huda Akil of the University of Michigan says. Less really may be more, at least when it comes to FGF9.

2 minute animation, (includes full body animation rendition of Australopithicus) A recent study of fossil shoulder bones from a human ancestor reveals that this ancient relative was still well adapted to living in trees, even after the evolution of bipedalism. Studying features like these helps scientists to better understand when modern humans moved away from a partly arboreal lifestyle and transitioned to living exclusively on the ground.

The news that researchers want to create human-animal chimeras has generated controversy recently, and may conjure up ideas about Frankenstein-ish experiments. But chimeras aren't always man-made-and there are a number of examples of human chimeras that already exist. A chimera is essentially a single organism that's made up of cells from two or more "individuals"-that is, it contains two sets of DNA, with the code to make two separate organisms.

The uproar over the new ease and precision with which scientists can manipulate the DNA of living things has centered largely on the complicated prospect of editing human embryos. But with the federal government's approval last week of a fast-growing salmon as the first genetically altered animal Americans can eat, a menagerie of gene-edited animals is already being raised on farms and in laboratories around the world - some designed for food, some to fight disease, some, perhaps, as pets.

In 1977, a University of Oxford statistician named Richard Peto pointed out a simple yet puzzling biological fact: We humans should have a lot more cancer than mice, but we don't. Dr. Peto's argument was beguilingly simple. Every time a cell divides, there's a small chance it will gain a mutation that speeds its growth. Cells that accumulate several of these mutations may become cancerous. The bigger an animal is, the more cells it has, and the longer an animal lives, the more times its cells divide. We humans undergo about 10,000 times as many cell divisions as mice - and thus should be far more likely to get cancer.

Since 2003, the H5N1 influenza virus, more commonly known as the bird flu, has been responsible for the deaths of millions of chickens and ducks and has infected more than 650 people, leading to a 60 percent mortality rate for the latter. Luckily, this virus has yet to achieve human-to-human transmission, but a small number of mutations could change that, resulting in a pandemic. Now a team of investigators from St. Jude Children's Research Hospital, Stanford University Medical Center, and MacroGenics have developed an antibody which has proven 100 percent protective against the virus in two species of animal models.

For the first time, biologists have succeeded in growing human stem cells in pig embryos, shifting from science fiction to the realm of the possible the idea of developing human organs in animals for later transplant.

Scientists have genetically engineered monkeys so that they exhibit behaviors similar to autism, with a goal of testing potential therapies on the animals in hopes that their resemblance to humans will yield more answers about the disorder. The scientists found that the monkeys showed "very similar behaviors related to human autism patients, including repetitive behaviors, increased anxiety and, most importantly, defects in social interactions," said Zilong Qiu, a leader of the research at the Institute of Neuroscience at the Chinese Academy of Sciences in Shanghai. The team is now imaging the brains of the monkeys, he said, "trying to identify the deficiency in the brain circuits that is responsible for the autism-like behavior."

Species like yeast, flies, fish and mice have many genes in common with humans and are therefore considered 'model organisms' and are widely used in research to study human genes and human diseases. Mouse research has lead to major advances in our ability to treat a number of serious diseases and conditions.

While humans and mice look and act very differently, 85 to 90 percent of our genes are the same or similar. So if scientists can understand the instructions in every mouse gene, people will get a good idea of the instructions in virtually every human gene as well.

Humans, like all animals, need sleep, along with food, water and oxygen, to survive. For humans sleep is a vital indicator of overall health and well-being. We spend up to one-third of our lives asleep, and the overall state of our "sleep health " remains an essential question throughout our lifespan. Most of us know that getting a good night's sleep is important, but too few of us actually make those eight or so hours between the sheets a priority. For many of us with sleep debt, we've forgotten what "being really, truly rested" feels like.

A cornerstone of modern biomedical research is the use of mouse models to explore basic pathophysiological mechanisms, evaluate new therapeutic approaches, and make go or no-go decisions to carry new drug candidates forward into clinical trials. Systematic studies evaluating how well murine models mimic human inflammatory diseases are nonexistent. Here, we show that, although acute inflammatory stresses from different etiologies result in highly similar genomic responses in humans, the responses in corresponding mouse models correlate poorly with the human conditions and also, one another.

BioLEAP is a comprehensive educational resource for students who do not wish to take part in classroom dissection exercises, and for teachers and school districts looking to introduce dissection alternatives into their curricula. These "alternatives" are really "advancements" in teaching tools that capitalize on 21st century technologies that can enhance a student's understanding of anatomy, physiology and the life sciences in general. The following links will provide you with cost-effective and humane alternatives to animal use in the classroom, as well as provide you with information about student choice laws and policies that protect students' rights to use dissection alternatives.

Normally, male squirrel monkeys can't distinguish between red and green hues-they're what is called color-blind in humans. The South American Saimiri genus lacks a gene that allows color-sensitive cells in the eye, called cones, to differentiate red and green from gray. To these animals, other colors, such as blue, brown and orange, appear faded. But Sam was one of two males in the experimental group of a groundbreaking 2009 ophthalmological study conducted at the Washington National Primate Research Center in Seattle. Husband-and-wife vision researchers Jay and Maureen Neitz injected a viral vector behind the retinas, the part of the eye that responds to color, of Sam and his simian lab partner, Dalton. The virus contained the genetic code in human eyes for red pigment, giving the monkeys an extra class of cone photoreceptor.