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Ethical, Legal, and Social Issues This page is an archive, the contents of which provide a snapshot in time--describing potential societal concerns arising from increased knowledge of our personal DNA as described and studied during the HGP (1990-2003). The content of this page is as it was at the close of the project with the exception of minor repairs such as the removal of broken links. The U.S. Department of Energy (DOE) and the National Institutes of Health (NIH) devoted 3% to 5% of their annual Human Genome Project (HGP) budgets toward studying the ethical, legal, and social issues (ELSI) surrounding availability of genetic information.

APA Format for Nursing School Books: Drug Guides, Care Plans & More After 20-plus pages of writing and hours of research, a student’s head may be a bit scrambled. Therefore, we created this list to help those in such predicaments. This page includes a list of resources commonly used by nursing students in school. Each reference is formatted in APA style and organized by reference type in order to make them easily accessible for academic compositions, school projects, nursing care plans, and other assignments. The Ten Most Disturbing Scientific Discoveries Science can be glorious; it can bring clarity to a chaotic world. But big scientific discoveries are by nature counterintuitive and sometimes shocking. Here are ten of the biggest threats to our peace of mind. 1. The Earth is not the center of the universe. We’ve had more than 400 years to get used to the idea, but it’s still a little unsettling.

PennCNV PennCNV: copy number variation detection Welcome! PennCNV is a free software tool for Copy Number Variation (CNV) detection from SNP genotyping arrays. Currently it can handle signal intensity data from Illumina and Affymetrix arrays. With appropriate preparation of file format, it can also handle other types of SNP arrays and oligonucleotide arrays. Researchers Find Evidence of Ancient Human History Encoded in Music’s Complex Patterns Newswise — HAMILTON, ON, November 19, 2013 — In the same way that fragments of ancient pottery and bones offer valuable information about human history, music can also reveal previously hidden clues about the past, according to new research from an international team led by McMaster University psychologist Steven Brown. The team has established for the first time that the history of human populations is embedded in music, where complex combinations of rhythm, pitch and arrangement form a code that scientists can read in a manner that can be compared to the way they read changes in human DNA and language. “Music is an untapped migrational marker that can be used to help people understand the history of human populations,” says Brown, an associate professor of Psychology, Neuroscience & Behaviour.

American Porphyria Foundation Click on the bold blue text below or on a topic listed on the left side of the page to read more. Porphyria is not a single disease but a group of at least eight disorders that differ considerably from each other. A common feature in all porphyrias is the accumulation in the body of porphyrins or porphyrin precursors. Although these are normal body chemicals, they normally do not accumulate.

10 Websites To Make You Think Supposedly browsing the internet requires more brain power than watching television. Although judging from some of the websites we’ve come across that assumption is cast into doubt. Here’s some of the sites we like that might get your brain to sit up and listen. Ted A conference that started in 1984 bringing together experts in technology, entertainment and design quickly grew into so much more.

ASHG 2010: 1000 Genomes Project Tutorials ASHG 2010: 1000 Genomes Project Tutorial Videos The 1000 Genomes Project has released the data sets for the pilot projects and for more than 1000 samples for the full-scale project. A tutorial for how to use the data was held at the 2010 American Society of Human Genetics (ASHG) annual convention on November 3. Videos for each of the tutorial sessions are now available. The tutorial describes 1000 Genomes Project data, how to access it and how to use it. Each of the speakers and their topics are listed below along with their tutorial videos and PowerPoint slides. Capturing a hard-wired variability: What makes some identical twins noticeably different? A Ludwig Cancer Research study has uncovered a phenomenon that alters prevailing views of how the genome is expressed to make and sustain the life of mammals. Published in the journal Science, the paper helps explain why genetically identical animals are sometimes so different in their biology and appearance, and why some inherited disorders caused by a shared set of aberrant genes can be of such variable severity in different people. "We have captured a fundamental randomness at the level of gene expression that has never before been described -- one that persists throughout development and into adulthood," says Ludwig scientist Rickard Sandberg at the Karolinska Institutet in Sweden. The discovery was made possible by a powerful new technique developed by Sandberg's lab for analyzing the global expression of genes in single cells.

Department of Neurobiology and Anatomy - The University of Texas Medical School at Houston Welcome to Neuroscience Online, the Open-Access Neuroscience Electronic Textbook This online, interactive courseware for the study of neuroscience is provided by the Department of Neurobiology and Anatomy at The University of Texas Medical School at Houston. The project is being developed under the direction of the Department Chair and Editor, John H.

Teacher Tools & Templates - Venn Diagram Happy Thanksgiving! Template Graphic Organizer TemplatesBack to Top Holiday Gift Coupon TemplatesBack to Top Seasonal / Holiday Work Sheets & TemplatesBack to Top Get timely coloring and activity sheets. Plus, use the holiday/special day templates to create themed work sheets (type a math problem, fill-in-the-blank sentence, etc. into a holiday silhouette). Icebreaker TemplatesBack to Top For use with icebreakers and other classroom lessons and activities. Language Arts TemplatesBack to Top Mathematics / Science TemplatesBack to Top Miscellaneous TemplatesBack to Top Newsletter TemplatesBack to Top Parent-Teacher Communication TemplatesBack to Top Communicate with parents by snail mail or e-mail with these editable and/or printable forms and letters. Setting Goal TemplatesBack to Top Student Resources TemplatesBack to Top Teacher-Quote Notepad TemplatesBack to Top Personalize these teacher notepads and print them.

PLINK This page describes some basic file formats, convenience functions and analysis options for rare copy number variant (CNV) data. Support for common copy number polymorphisms (CNPs) is described here. Copy number variants are represented as segments. These segments are essentially represented and analysed in a similar manner to how PLINK handles runs of homozygosity (defined by a start and stop site on a given chromosome). Allelic (i.e. basic SNP) information is not considered here: PLINK skips the usual procedure of reading in SNP genotype data.

Naturally blond hair in Solomon Islanders rooted in native gene, study finds © Sergio Piumatti Researchers have identified a gene that is responsible for blond hair in 5-10 percent of the indigenous population of the Solomon Islands in the South Pacific. The common occurrence of blond hair among the dark-skinned indigenous people of the Solomon Islands is due to a homegrown genetic variant distinct from the gene that leads to blond hair in Europeans, according to a new study from the Stanford University School of Medicine. “This is one of the most beautiful examples to date of the mapping of a simple genetic trait in humans,” said David Reich, PhD, a professor of genetics at Harvard University, who was not involved in the study. The study identifying the gene responsible for blond hair in the Solomon Islands, a nation in the South Pacific, represents a rare case of simple genetics determining human appearance, and shows the importance of including understudied populations in gene mapping studies, said co-senior author Carlos D.

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