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This initial module from the GENIQUEST project introduces the dragons and the inheritance of their traits, then delves into meiosis and its relationship to inherited traits. Students examine the effects of choosing different gametes on dragon offspring, and learn about genetic recombination by creating recombination events to generate specific offspring from two given parent dragons. Students learn about inbred strains and breed an inbred strain of dragons themselves. Lastly, students investigate a mysterious new dragon trait and use the properties of linkage and inheritance to examine the trait's relationship to other, known dragon traits.

When babies are born, their eyes and hair are one color, but change within the first few years of their life! Why do hair and eye colors change? Trace explains the process of inheriting certain traits from your parents, and discusses why the colors change!

The Rare Disease Foundation is focussed on linking basic science and clinical practice to increase the efficiency of rare disease research. This model is called Translational Care. This model drives patient based, treatment focussed research projects from disease characterization to treatment with greater efficiency. By incorporating research, astute clinician observation and parental knowledge into the various stages of rare disease research we impact the speed of discovery and the way rare conditions are managed.

The 18-year-olds from Gloucester, U.K. are two of the five children born to their Caucasian father and "half-Jamaican" mother, World Wide Features reports. While their other siblings have a blend of features from their parents, Lucy and Maria are opposites: Lucy has fair skin and red hair, while Maria has caramel skin and dark hair.

Welcome to BioEd Online, the online educational resource for educators, students, and parents. BioEd Online utilizes state-of-the-art technology to give you instant access to reliable, cutting-edge information and educational tools for biology and related subjects. Our goal is to provide useful, accurate, and current information and materials that build upon and enhance the skills and knowledge of science educators. Developed under the guidance of our expert Editorial Board, BioEd Online offers the following high-quality resources.

Most siblings with a diagnosis of autism do not share the same genetic risk factors for the disorder and are as distinct in their behaviors as any brothers and sisters, scientists reported on Monday in a study that came as a surprise to many doctors, if not to parents.

ach of the four hallmarks of autosomal dominant inheritance are fulfilled. Each affected individual has an affected parent; there is no skipping of generations. Males and females are equally likely to be affected. About 1/2 of the offspring of an affected individual are affected (the recurrence risk is 1/2). Normal siblings (II-3) of affected individuals have all normal offspring.

HPV is considered one of the most common sexually transmitted infections, and it affects both men and women! Is it dangerous, and can it be prevented? Get your official DNews t-shirt here: http://www.forhumanpeoples.com/collec... Read More: Genital HPV Infection - Fact Sheet http://www.cdc.gov/std/hpv/stdfact-hp... "Human papillomavirus (HPV) is the most common sexually transmitted infection in the United States. Some health effects caused by HPV can be prevented with vaccines." Time To Rethink 'Girls-Only' Approach To HPV Vaccine? http://www.futurity.org/hpv-vaccines-... "Encouraging parents to have their sons get the human papillomavirus (HPV) vaccine-rather than just trying to get more girls vaccinated-could ultimately protect more people for the same price, according to a study by a mathematician."

Using a pre-drawn template can be helpful during a consultation to explain single gene inheritance. Our template shows one pair of chromosomes for each parent. Each chromosome has a single gene highlighted that can be coloured in to illustrate a gene alteration. You can then show which sperm and/or eggs contain the chromosome with the gene alteration and the different genetic combinations that could be present at conception.

In biology classes, students are typically taught that spontaneous generation does not take place. And yet, at the origin of life, life had to arise without parents from abiotic processes. What were those processes that gave rise to the first life?  This case study uses an interrupted format to guide students through the Miller-Urey experiment of 1953, which showed that organic molecules could be produced from abiotic precursors and conditions thought to be prevalent on the early Earth. The case also addresses the more speculative implications about where these reactions may have taken place to create the organic building blocks of life on this planet. The first three parts of the case, which explore the Miller-Urey experiment, are ideal for introductory biology courses and take about 45-50 minutes to complete. The remaining sections, which explore whether such chemical reactions took place in outer space, were used in a non-major astrobiology course and require a further hour to complete.

7:00 video: This film is the first of a two part series on the evolution of new genetic information. Here we focus on Point Mutations - the simplest natural mechanisms known to increase the genetic information of a population. Our second film of the series will focus on duplication events - natural mutations that increase the total amount of genetic information of an individual. This film was produced under the guidance of molecular biologist Dr. Nicholas Casewell. http://www.lstmed.ac.uk/about/people/... Point mutations are small, natural edits in the DNA code of an individual. These edits can be passed from parent to child. Because they are mere edits, point mutations usually do not increase the total amount of information in an individual. As new information is gained, old information is lost. Point mutations do, however, increase the total amount of information within a population. In this film you will see several examples of beneficial point mutations which have enhanced a creatures abilities or even given rise to entirely new abilities. The first two examples were directly observed in bacteria by scientists in the lab. The third is a case found in domestic dogs, the last example was discovered in several species of wild animal.

Scientists were investigating a tantalizing but controversial hypothesis: that a man's experiences can alter his sperm, and that those changes in turn may alter his children.

This interdisciplinary case study uses the format of a progressive disclosure to explore certain advances in biotechnology and evaluate them within the framework of societal needs, concerns and pressures.  When faced with a heart valve transplant, a high school student and her mother must decide between multiple approaches, some current and others emergent. Highlighted in this case study are the topics of xenotransplantation, 3D bioprinting and the mature minor rule. The case includes a role-playing, public hearing activity that can be used to explore many aspects at the interface of technology and culture: religious rights, parental rights, public health care policy and safety, animal rights, economic issues of organ marketing, and psychological issues of body image.  This case study was originally designed for first year collegiate classes (introduction to biology, introduction to psychology) but is also applicable to AP high school. The flexible nature of the case also allows for expansion of several aspects for advanced classes across multiple disciplines.

Flinn Scientific has launched a website with an extensive amount of resources specifically developed to help teachers, students and parents continue their science education journey - even if that learning is taking place outside the classroom or laboratory environment. Examples of some of the resources we have developed: Free video labs with related teacher and student guides to help students at home continue making progress on key science topics More than 40 free, easy and fun-to-do activities that use commonly available materials to encourage science investigation in the home Flinn's unique digital learning solutions to facilitate seamless science learning. These online solutions are the perfect way to efficiently scale curriculum in an at-home setting - also free of charge On call scientists: over the coming days, we will be releasing video based lab experiments conducted by our scientific staff and broadcast from our studio with live events. As part of each live event, we will have our full team of scientists available to answer questions from teachers and students participating online - also free of charge and highly interactive and engaging. Be sure to check out our online calendar indicating the live schedule

This case study is designed to teach basic concepts of genetics by focusing on a rare disease, pseudoxanthoma elasticum (PXE).  Chromosome 16 is the narrator at the beginning of the case and introduces students to genes, chromosomes and mutations. The focus then shifts to the patient and his mother as she finds out about her son's disease and her subsequent efforts to connect with patient advocacy groups for support. The case concludes with students watching a TED talk given by Sharon Terry, the real-life mother on whom this story is loosely based, so that students can connect on an emotional and human level with someone who has intimate experience as a parent of children with a rare genetic disease. The case is suitable for high school general biology classes, but it can also be used by biology major or non-major undergraduates in a lower-division biology class, or in any lower-division non-major class focused on human disease.

Say a red gummy bear has a baby with a yellow gummy bear - what percentage of red and yellow do the parents give to their children? Well, assuming gummy bear genetics works the same way we do, they'll have one set of chromosomes from their mum and one from their dad - so 50 percent from each - easy!

Scientists don't fit a mold - the stories we tell about them shouldn't either. We've created scientist-of-the-month toolkits for teachers, parents/guardians, and informal educators to easily share these stories with their students.

This "clicker case" tells the story of "Hannah," a baby girl adopted by two loving parents who grows up with an uncontrolled appetite and develops severe early-onset obesity. Students follow Hannah's story as she develops excessive eating early in life, which her health care team is unable to explain. A visit to obesity specialists finally reveals the underlying cause of Hannah's obsession with food: extremely low levels of circulating leptin, a hormone that regulates appetite and body weight. It is further discovered that Hannah's leptin deficiency is due to a mutation in the LEP gene. As the story unfolds, students first work on unit conversions and BMI calculations to practice quantitative skills as well as graph and data interpretation skills. Students then apply their knowledge of DNA transcription, translation, and protein structure to answer questions based on figures from a 2019 study on LEP mutations. The case is best suited for high school and lower-level undergraduate biology courses.

Mitochondrial diseases are a group of disorders caused by genetic mutations. In this animation, Nature Video finds out how these diseases arise, and how new techniques can stop them being passed on from mother to child.

We recently asked school nurses, "What's the most important thing teachers can do to help keep students healthy during the school year?"