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This flipped clicker case study explores the fascinating relationship between the Arizona Bark Scorpion (the most venomous scorpion in North America) and the Southern Grasshopper Mouse. Initially it would seem that the grasshopper mouse is no match for the scorpion's venom; however, the grasshopper mouse is easily able to eat the scorpion and is largely immune to the scorpion's sting. By working through this case study, students learn about neuron anatomy and physiology as they explore how the grasshopper mouse is able to survive the scorpion's venom. This case study was developed for an introductory biology course for majors, but it could also be used in an introductory biology course for non-majors or in an anatomy and physiology course. The case requires that students learn basic neuron anatomy and action potential physiology prior to class by reading their textbook or by watching videos on the subjects. An optional set of guided questions tailored to Campbell Biology (10th ed.) is included in the teaching notes.

The mouse is a common model used in research as a way of studying human biology and diseases, but a new study questions whether this is an accurate approach considering some stark differences - aside from many similarities - between the two species.

The mouse is the leading organism for disease research. A rich resource of genetic variation occurs naturally in inbred and special strains owing to spontaneous mutations. However, one can also obtain desired gene mutations by using the following processes: targeted mutations that eliminate function in the whole organism or in a specific tissue; forward genetic screens using chemicals or transposons; or the introduction of exogenous transgenes as DNAs, bacterial artificial chromosomes (BACs) or reporter constructs. The mouse is the only mammal that provides such a rich resource of genetic diversity coupled with the potential for extensive genome manipulation, and is therefore a powerful application for modeling human disease.

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.

A data collection and analysis lesson that examines selection for coat color in pocket mouse populations on different color substrates over time.

Existing mouse models of lethal Ebola virus infection do not reproduce hallmark symptoms of Ebola hemorrhagic fever, neither delayed blood coagulation and disseminated intravascular coagulation, nor death from shock, thus restricting pathogenesis studies to non-human primates. Here we show that mice from the Collaborative Cross exhibit distinct disease phenotypes following mouse-adapted Ebola virus infection. Phenotypes range from complete resistance to lethal disease to severe hemorrhagic fever characterized by prolonged coagulation times and 100% mortality. Inflammatory signaling was associated with vascular permeability and endothelial activation, and resistance to lethal infection arose by induction of lymphocyte differentiation and cellular adhesion, likely mediated by the susceptibility allele Tek. These data indicate that genetic background determines susceptibility to Ebola hemorrhagic fever.

Millions of people suffer from asthma, a frightening disease that makes you feel like you're drowning. Using both mouse and human cells - and a humanized mouse to show how human type 2 innate lymphoid cells (ILC2) work in the body, researchers at Janssen Research and Development, Dana-Farber Cancer Institute and Harvard Medical School are figuring out ILC2's role in asthma. Their findings have important implications in the quest for effective asthma therapies!

With a dozen or so 140-character dispatches (including three heat maps), Gilad suggested the results published in PNAS were an anomaly-a result of how the tissue samples were sequenced in different batches. If this "batch effect" was eliminated, he proposed, mouse and human tissues clustered in a tissue-specific manner, confirming previous results rather than supporting the conclusions reported by the Mouse ENCODE team.

3 min video, Scientists have made a major advancement in the world of cloning-- creating hundreds of identical mice from a single drop of blood. The implications are pretty big. Why? Anthony Carboni as the answers.

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.

Mouse study fingers potential cause of fertility problems, proposing obesity and egg quality link.

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.

" An anti-cancer drug reverses memory deficits in an Alzheimer's disease mouse model, University of Pittsburgh Graduate School of Public Health researchers confirm in the journal Science."

Summary of agouti mouse research into epigenetics as well as epigenetics and cancer summary.

Summary of mouse study looking at neurogenerative differences in mice.

Embryo Images Normal and Abnormal Mammalian Development is a tutorial that uses scanning electron micrographs (SEMs) as the primary resource to teach mammalian embryology. The 3-D like quality of the micrographs coupled with selected line drawings and minimal text allow relatively easy understanding of the complex morphological changes that occur in utero. Because early human embryos are not readily available and because embryogenesis is very similar across mammalian species, the majority of micrographs that are utilized in this tutorial are of mouse embryos. The remainder are human.

Biologists at the Massachusetts Institute of Technology have created a genetically modified version of a common bacteria found in the gut that can sense the environment there and fight disease. And when this designer bacteria works, the proof is in the poop - glowing poop. (In this case, mouse poop.)

Like many newborn mammals, baby mice cry to get their mother's attention. But the mother doesn't instinctively recognize these calls; she must learn the sounds of her offspring-just as human parents must learn the cries of their infants. Now, a team of researchers has discovered that the hormone oxytocin, which has been tied to trust and maternal bonding, holds the key to how this learning occurs. Only after oxytocin  tweaks the brain of a female mouse does she respond with a mother's concern and attentiveness to crying pups.

In the Oct. 30 edition of Science, scientists describe strains of laboratory mice bred to test the role of an individual's genetic makeup in the course of Ebola disease. Systems biologists and virologists Angela Rasmussen and Michael Katze from the Katze Laboratory at the University of Washington Department of Microbiology led the study in collaboration with the National Institutes of Health's Rocky Mountain Laboratories in Montana and University of North Carolina at Chapel Hill.

Cattle with the mouse gene SP110 added to their genomes have immune cells that are better at slowing the growth of Mycobacterium bovis and are less susceptible to developing the internal symptoms of tuberculosis (TB), according to a study published this week (March 2) in PNAS.