41. Gene Blues | Bullfrog Films gene Blues Dilemmas of (dna) testing Examines the ethical issues associatedwith (dna) testing. 30 minutes Color Grade Level 912, College http://www.bullfrogfilms.com/catalog/gene.html

Search tips PRICING / ORDER To order this video select one choice below then click "Add to Order" (You can also use this process to generate an order form for faxing or mailing.) Purchase:* Rent:* Preview * Reduced rates for activists and grassroots groups. Please inquire. Preview Policy License Agreement ORDER INFO Bullfrog Films P.O. Box 149 Oley, PA 19547 Tel: 610/779-8226 Fax: 610/370-1978 Gene Blues Dilemmas of DNA Testing Examines the ethical issues associated with DNA testing. 30 minutes Color Grade Level: 9-12, College, Adult US Release Date: 1997 ISBN: 1-56029-715-8 Directed by Mark Dworkin and Melissa Young Produced by Moving Images "A brilliant look at the social implications of genetic knowledge." Sheldon Krimsky, Tufts University This outstanding video examines some of the ethical issues associated with DNA testing and sets the stage for a national debate on the ramifications of human gene technology. As geneticists unlock the DNA code, they learn how differences in the DNA that makes up particular genes are linked to variations in physical traits - from an organism's size to its resistance or susceptibility to disease. While this knowledge holds promise for alleviating human suffering, DNA testing has presented real problems, including

42. Genetics Education Center Resources for educators interested in human genetics and the human genome project. The site is maintained Category Science Biology genetics Education...... JCBrown, Microbiology, University of Kansas; What is gene testing? Lawrence BerkeleyLab; Winding Your Way Through (dna), University of California, San Francisco http://www.kumc.edu/gec/

Genetics Education Center University of Kansas Medical Center For educators interested in human genetics and the human genome project Human Genome Project Resources (books, videos, curricula) Lesson Plans Networking Genetic Conditions Careers ... Search The Human Genome Project National Human Genome Research Institute (NHGRI), National Institutes of Health (NIH), Human Genome Project Glossary of Genetic Terms Educational Resources Genetic Variation ... Fact Sheets New Department of Energy Human Genome Program (DOE), Education Human Genome Project Molecular Genetics Primer Science Behind the Project ... The Human Genome Project: Exploring Our Molecular Selves , Multimedia Education Kit, NHGRI, DOE, Science, Nature, HHMI, Pharma, ASHG Genome Gateway , Nature Publishing Company New Human Genome , National Center for Biotechnology Information (NCBI) of the National Library of Medicine (NLM) New Human Genome Teacher Networking Project - Univ. Kansas Medical Center Human Genome Centers - background, goals, developments Genetic Education Resources Resources curricula books videotapes ... Genetic Lesson Plans - from teachers in KUMC and other programs Genetic Conditions - support groups, addresses, links

43. Genetics Resource Materials For Teachers key genetic concepts, science, potential benefits, potential risks of gene testing; WindingYour Way Through (dna), genetics symposium, University of California http://www.kumc.edu/gec/resource.html

Genetics Education Materials Resource List Books ( annotated or short list) Hands-on Materials Computer Programs Curricula Videotapes ( 1992 to present or comprehensive annotated list Booklets/Brochures Genetic Journals , hum-molgen ... Posters Other: The Human Genome Project , MCET, Boston, MA, deal with the ethical, legal, and social implications of genetic information and its dissemination. Includes student projects, teacher resources, and interactive material. Genetics Education Unit genetics unit, ethics unit, N.S.W. Genetics Education Program including student center and Victorian Certificate of Education, Murdoch Institute, Australia Kids writing that report for school on Huntington disease Blazing a Genetic Trail - online book, Howard Hughes Medical Institutes. Includes information on Basic Genetics the Human Genome Project Glossary Oliver Sacks: The Mind Traveler a four part BBB / PBS television series: 1) Rag' Cajun (Usher's Syndrome - deafness and blindness), 2) The Island of the Colorblind (Pingelap, a Pacific atoll, ten percent of the population is colorblind), 3) Rage for Order (Autism), and 4) Don't Be Shy, Mr. Sacks (Williams Syndrome) How a human cell acts like a computer DNA: The Instructional Manual for All Life (many on genetics) A Genetics Role-playing Activity by SNelson Access Excellence Genetic Lesson Plans Genetic Health Forum TProfit Developing a Pedigree of a Family Tree , ABiggs

44. Genetic Screening For Breast Cancer Provides Answers For Some Patients for (dna) test results and understand the psychological impact test results may haveon their family and relationships. Some patients testing positive for a gene http://healthlink.mcw.edu/article/972932220.html

Search Articles: search tips Please Take the HealthLink Survey Email this article Print this article Find related articles: By topic: Cancer Genetics By keywords: Genetic Screening gene testing gene mutations Receive Health Link via email! Subscribe now >> Genetic Screening for Breast Cancer Provides Answers for Some Patients While only 5-10% of all cancers have an inherited, genetic component, there are DNA tests available to diagnose gene mutations that put women at a significantly increased risk for breast cancer. Programs like the Froedtert and Medical College Cancer Genetic Screening Program offer genetic counseling and testing to individuals who may be at increased risk of breast cancer based on their personal or family history of cancer. The genes, known as BRCA1 and BRCA2, hold the key to genetic testing for breast cancer. Mutations of these genes account for about 80% of inherited breast cancers, and also signal an increased risk of ovarian cancer. Genetic testing requires only a small blood sample from the patient. However, the test itself involves sophisticated molecular techniques in which DNA is extracted from white blood cells and is then sequenced. Only one laboratory in the nation (located in Salt Lake City) conducts full DNA sequencing. Average turnaround time is three to four weeks. The cost is about $2600, plus about $150 for genetic counseling. Insurance coverage is variable depending on the policy and medical history of the individual seeking testing.

45. DNA Chip - Genetic Testing Of The Future Scanning methods involve testing the gene or genes could potentially interact withthe diseasecausing gene. truncation, and just recently (dna) chip technology http://www.ndsu.nodak.edu/instruct/mcclean/plsc431/students99/althoff.htm

DNA Chip - Genetic Testing of the Future Lisa Althoff Many, if not most diseases, have their roots in our genes. Genes, through the proteins they encode, determine how efficiently we process foods, how effectively we detoxify poisons, and how vigorously we respond to infections. In the past 20 years, amazing new techniques have allowed scientists to learn a great deal about how genes work and how they are linked to disease. This rapid pace of discovery of genetic factors, responsible for certain diseases, has allowed scientists to genetically test asymptomatic individuals and predict their risk of certain diseases. In this paper, I am going to discuss the following areas pertaining to the topic of genetic testing: The definition and purpose of genetic testing Distinguishing major testing techniques with particular interest in the DNA chip Ethical considerations regarding genetic testing, explaining views on both sides Public policy pertaining to genetic testing and the use of the DNA chip and My personal opinion regarding the use of the DNA chip.

46. Pancreas Cancer FAQs the (dna) finding typical of HNPCC, called microsatellite instability has recentlybeen reported in a small (~4%) fraction of pancreas cancers. gene testing for http://pathology2.jhu.edu/pancreas/hered.cfm

The Pancreas Pancreatic Cancer Causes of PC Heredity ... Pain Management 4) Is pancreatic cancer hereditary? Cancer of the pancreas is a genetic disease which means that it is caused by changes (mutations) in DNA. These changes can be inherited (we are born with them) or they can be acquired (they develop after we are born). The inherited changes explain why cancer of the pancreas runs in some families, and the acquired changes can be the result of either bad luck during cell replication or by exposure to carcinogens (cancer causing chemicals) such as those found in cigarette smoke. This is a current area of research at Hopkins. It has been estimated that ten percent of pancreatic cancers are hereditary. Many of these occur as part of rare medical syndromes. These include: 1) Familial pancreatic cancer- It has now become clear that pancreas cancer by itself (not part of a known syndrome) runs in some families. For example, relatives of patients with pancreas cancer have an increased risk for developing pancreas cancer themselves, and the National Familial Pancreas Cancer Registry (NFPTR) now contains over 250 families in which two or more family members have had pancreas cancer. Scientists at Johns Hopkins are working diligently to discover the reasons why pancreas cancer runs in these families. Anyone wishing to join this registry or wishing to learn more about familial pancreas cancer may contact Kieran Brune at

47. FRAGILE X TESTING, DNA ANALYSIS FRAGILE X testing, (dna) ANALYSIS. TEST CODEFX(dna) CPT CODE83890,83892,83894,83896SYNONYMS FMR1 gene Mutation Analysis, RFLP Analysis TEST INCLUDES Southern http://hsc.virginia.edu/medicine/clinical/pathology/labtests/handbook/fxdna.htm

FRAGILE X TESTING, DNA ANALYSIS TEST CODE: FXDNA CPT CODE: SYNONYMS: FMR-1 Gene Mutation Analysis, RFLP Analysis TEST INCLUDES: Southern blot analysis using a polymorphic DNA probe specific for the FMR-1 gene. LABORATORY: Molecular Pathology SPECIMEN: Lavender Top (EDTA) MINIMUM VOLUME: 5 mL blood AVAILABILITY: By consultation only TURNAROUND TIME: 4 weeks SPECIAL INSTRUCTIONS: This test is appropriate for testing of affected individuals, carrier testing and prenatal diagnosis. Contact the Office of Clinical Laboratory Services (982-1898) or the Division of Clinical Genetics (924-2665). REFERENCE RANGE:

48. DNA Testing Forms you have received the FTA gene Cards obtain blood samples following instructionsgiven on Instructions for Collecting and Mailing FTA cards for (dna) testing. http://www.lamaregistry.com/dna.htm

New ILR Bar Code DNA Analysis Procedures Obtaining DNA Analysis for an as-yet-unregistered llama With the move to the use of FTA Gene Cards, the process for obtaining DNA analysis has been greatly simplified. Obtain a FTA Gene Card from the ILR Office for each llama you wish to register or have DNA analysis. When you have received the FTA Gene Cards obtain blood samples following instructions given on Instructions for Collecting and Mailing FTA cards for DNA Testing. Complete and mail to the ILR Application for Registration Listing Form, including all appropriate signatures, photographs and fees (fees include llama registration and DNA analysis charge) and FTA Gene Card. [If you have chosen to submit an FTA Gene Card for sample storage only, there is not fee for DNA analysis, and DNA analysis will not be completed.] When the registration is complete you will receive a DNA analysis report for your records. For details concerning the ILR Application for Registration see the following information or contact the Registry. Llama Registration Overview If you do not have access to the ILR web site, give us a call and we will send you a copy of the documents.

49. Advances And Opportunities In DNA Testing And Gene Probes This site has moved taking you to the new site in 2 seconds. If youdon't switch sites please click here. Sorry! - this publication http://www.textor.com/cms/dBUBI14.html

This site has moved - taking you to the new site in 2 seconds. If you don't switch sites please click here Sorry! - this publication has either been updated or is discontinued. Four simple ways to find an alternative product! Click Home to browse the subject index. Use the Search facility at the top of this page to locate a similar product. Phone us on for personal attention 8 a.m - 6 p.m. European time Mondays to Fridays. E-mail us with your requirements. Keep up-to-date on the latest publications and special offers! Just e-mail to register now - you will be kept up-to-speed on new business-to-business reports, newsletters, and directories - and you'll also be able to take advantage of special deals and price saving offers! And when you register, tell us what your interests are! Featured Titles: The Mobile Customer Experience Med Ad News Search title product code publisher key words

50. Back To Basics in genes (mutations) can cause diseases and what is involved in gene testing. Australia)Understanding genetics Shows how genes, chromosomes, (dna) and proteins http://www.science.org.au/scied/basics.htm

Australian Academy of Science home Science education Nova: Science in the news Primary Investigations Back to basics The sites listed below provide an excellent introduction to several basic science concepts. You can visit the links in sequence or use the annotations to select those that contain information most relevant to your interests. Annotated lists of sites are available for Atoms and molecules DNA and genes Electromagnetic radiation Energy ... The structure of the Earth and Weather and climate Atoms and molecules Chem4Kids (Andrew Rader Studios, USA) Atoms Introduces the concept that all matter is made up of small particles called atoms. Structure Describes what makes up an atom (electrons, protons and neutrons). Bonding Shows how atoms can combine with other atoms to form molecules. Ions Describes those atoms that have an electrical charge because they have gained or lost one or more electrons. This site's chatty style and simple diagrams make it user-friendly for beginners. Atoms, molecules, water, pH (Clermont College, University of Cincinnati, USA) Covers much of the same information as (above), but uses different analogies. Simple diagrams effectively illustrate concepts. You can click on highlighted words for brief definitions.

51. Analysis Tools For DNA-arrays Preprocessing, Two samples tools, Clustering methods, Tree viewers, Datamining, DNAarray multiple testing. Datamining, FatiGO, FatiGO (Datamining with gene Ontology). http://bioinfo.cnio.es/dnarray/analysis/

Bioinformatics Unit CNIO DNA arrays: Analysis Tools Preprocessing Viewers Clustering Differential Gene Expression ... Data Mining Preprocessing Preprocess DNA array data files: log-transformation, replicate handling, missing value imputation, filtering and normalization. The resulting dataset can be sent to our local DNA array analysis tools and to the EPclust (@EBI). Preprocessing Viewers Clustering Differential Gene Expression ... Data Mining Viewers PlotCorr. Compares two samples. SotaTree. Viewer for Sota Trees. Tree. Viewer for Newick Trees. Preprocessing ... Data Mining Unsupervised Clustering SOTA. Sotarray Server. Cluster. Hierarchical Clustering Server SOM. Self-Organizing Map Server SOM-Tree Server. It performs a Hierarchical Clustering on Self-Organizing Map result for Exploratory Analysis ... Data Mining Differential Gene Expression Pomelo Tool Preprocessing Viewers Clustering ... Data Mining Supervised Classification SVM SVM Predictions Preprocessing Viewers ... Data Mining Data Mining FatiGO (Data Mining with Gene Ontology) Gene Ontology Browser Preprocessing Viewers ... Data Mining Send comments to the webmaster Last rev. Monday 17 February 2003

52. Advances And Opportunities In DNA Testing And Gene Probes Search By Keyword. Browse Choose a subject http://www.allbookstores.com/book/1569653607

Search By: Keyword Title Author ISBN Browse: Choose a subject: Art Children's Books Christian Books History Gardening Horror Mystery Oprah Book Club® Photography Reference Romance Science Science Fiction Sports Technology Travel Art Children's Books Christian Books History ... Store Directory Advances and Opportunities in DNA Testing and Gene Probes Format: Hardcover Published: September 1996 ISBN: List Price: Pages: Publisher: Business Communications Company, Incorporated Add this book to your wish list View your wish list Click on this books subject categories to see related titles: Subjects Marketing General Subjects ... Add your own review! Search By: Keyword Title Author ISBN Browse: Choose a subject: Art Children's Books Christian Books History Gardening Horror Mystery Oprah Book Club® Photography Reference Romance Science Science Fiction Sports Technology Travel About Us Affiliate Program Contact Us Help ... Webmasters

53. American Medical Association -- Genetics 101 TOP. What is gene testing? gene testing involves examining a person’s (dna) forsome anomaly that could cause or increase the risk for a disease or disorder. http://www.ama-assn.org/ama/pub/printcat/4646.html

Press the print button on your browser. Click here to return to the previous page. Genetics 101 What are genetics and molecular medicine? How do genes work? How are genes linked to disease? What is gene therapy? ... What is the Human Genome Project? What are genetics and molecular medicine? While its practical implications are broad, genetics essentially is the study of how specific biological traits and characteristics are transmitted to us by our parents. Molecular medicine examines how illness and disease occurs or can be prevented at the cellular or molecular level. TOP A cell is the individual unit from which tissues of the body are formed DNA is the double-stranded molecule that encodes genetic information in the nucleus of cells. A DNA strand is composed of four different nucleotides or base pairs (adenine, guanine, cytosine, and thymidine). It determines the structure, function and behavior of the cell. In animals and plants, long strands of DNA are arranged into structures called chromosomes Genes are sometimes known as the physical unit of heredity. Genes are formed from DNA, carried on the chromosomes and are responsible for the inherited characteristics that distinguish one individual from another. Each human individual has an estimated 30,000 separate genes.

54. Fragile X Syndrome A Policy Statement from the American College of Medical genetics.Category Health Conditions and Diseases Fragile X Syndrome...... When the mother is a known carrier, (dna) testing can be offered to determinewhether the fetus inherited the normal or mutant FMR1 gene. http://www.faseb.org/genetics/acmg/pol-16.htm

Policy Statement: American College of Medical Genetics Fragile X Syndrome: Diagnostic and Carrier Testing Introduction Fragile X syndrome is the most common cause of inherited mental retardation, seen in approximately one in 1,200 males and one in 2,500 females. Males with fragile X syndrome usually have mental retardation and often exhibit characteristic physical features and behavior [Hagerman and Silverman, 1991; Warren and Nelson, 1994]. Affected females exhibit a similar, but usually less severe phenotype. The diagnosis of fragile X syndrome was originally based on the expression of a folate-sensitive fragile site at Xq27.3 (FRAXA) induced in cell culture under conditions of folate deprivation. Cytogenetic analysis of metaphase spreads demonstrates the presence of the fragile site in less than 60% of cells in most affected individuals. The cytogenetic test has limitations, especially in testing for carrier status, and it exhibits a high degree of variability between individuals and laboratories. Also, interpretation of the cytogenetic test for fragile X syndrome is complicated by the presence of other fragile sites in the same region of the X chromosome (FRAXD, FRAXE, and FRAXF). Males and females carrying a premutation are unaffected. Male carriers are referred to as "normal transmitting" males, and they pass on the mutation, relatively unchanged in size, to all of their daughters. These daughters are unaffected, but are at risk of having affected offspring. Variable clinical severity is observed in both sexes. Most, but not all, males with a full mutation are mentally retarded and show typical physical ant behavioral features. Of females with a full mutation, approximately one-third are of normal intelligence, one-third are of borderline intelligence, and one-third are mentally retarded.

55. The Gene Letter By GeneSage - Archives The report, Postconviction (dna) testing Recommendations for Handling Requests, is one of a series that will be released by the National Institute of Justice http://www.genesage.com/professionals/geneletter/features/forensics.html

Browse Current Issue Browse Previous Issues Browse Previous Content Search GeneLetter Archives All GeneLetter Resources Discussions Surveys February 1, 2000 FEATURE ARTICLE National Report Acknowledges the Power of DNA Forensics The National Commision on the Future of DNA Evidence issues a report which could result in prosecuting the guilty and exonerating the wrongfully convicted. By Philip R. Reilly, MD, JD Traditionally, conviction and the exhaustion of subsequent appeals have marked the end of criminal case proceedings. However, technologoical advances in DNA forensic analysis offer new ways in evaluating evidence to both convict the guilty as well as correct previous miscarriages of justice. The National Commission on the Future of DNA Evidence (http://www.ojp.usdoj.gov/nij/pubs-sum/177626.htm) has issued recommendations on the use of DNA evidence in cases in which a person convicted of a crime seeks testing to overturn the verdict. The report, "Postconviction DNA Testing: Recommendations for Handling Requests," is one of a series that will be released by the National Institute of Justice (http://www.ojp.usdoj.gov/nij) over the next two years. The need for a study concerning postconviction DNA forensics became clear as early as 1995 in the form of a report directed by Cardozo Law School Professor Barry Sheck. Titled "The Innocence Project", this report compiled an impressive record of the release of approximately 75 individuals who had been convicted of rape largely on the basis of eyewitness evidence when post-conviction testing of a semen stain found at the crime scene did not match the DNA of the incarcerated men.

56. The Gene Letter By GeneSage - Archives Myotonic dystrophy type 1 (dna) testing. a naturallyoccurring repeat of a short nucleotidesequence (CTG) in the myotonic dystrophy protein kinase (DMPK) gene. http://www.genesage.com/professionals/geneletter/05-01-00/journalwatch/dm.html

NEW REVIEWS GENELETTER ARCHIVES All GeneLetter Resources Discussions Surveys May 15, 2000 JOURNAL WATCH REVIEW Myotonic dystrophy type 1 DNA testing The most common form of myotonic dystrophy (DM1) results from the expansion of a naturally-occurring repeat of a short nucleotide sequence (CTG) in the myotonic dystrophy protein kinase (DMPK) gene. However, several additional myotonic dystrophy syndromes have been described that do not involve this gene. These include proximal myotonic myopathy (PROMM), proximal myotonic dystrophy (PDM), and myotonic dystrophy type 2 (DM2). Attendees of the International Myotonic Dystrophy Consortium Conference (IMDCC) held in April 1999 decided to refer to these disorders collectively as the "myotonic dystrophies," and to name the genetic loci DM1, DM2, etc. - the group provides guidelines for DM testing in a recent paper Molecular diagnosis of DM1 is based on measurement of the size of the CTG repeat expansion. Five to 35 CTG repeats occur in the general population; 35-49 repeats places an individual at risk for developing DM1; and more than 50 CTG repeats correlates with the disorder. The IMDCC made recommendations on various testing scenarios, including testing symptomatic individuals to arrive at a clinical diagnosis, presymptomatic testing, testing of minors, and prenatal testing. Finally, the IMDCC stressed the importance of maintaining confidentiality of genetic information and respecting the rights of individuals on how their DNA is used for future testing.

57. Fool.com: Corning Muscles In On DNA Chips [News] September 14, 2000 Biochips (or (dna) chips, (dna) arrays or microarrays) are essential for genomics on them? Decoding the human genome has made the whole genetesting business much http://www.fool.com/news/2000/glw000914.htm

CHOOSE A BROKER Search: Quotes: Today's Headlines 401(k) 60-Second Guides Advisors ... About Us/Press Corning Muscles in on DNA Chips Advanced materials powerhouse Corning believes that making DNA chips will marry its expertise with big profits. But the company joins an emerging growth market filled with competition and patent lawsuits. The players are betting that a $1 billion pie in five years is only the start, and picking a winner now is anybody's guess. By Tom Jacobs (TMF Tom9) September 14, 2000 Fiber optic king Corning (NYSE: GLW) surprised the biotech world when it announced that it would enter the growth market for DNA chips. Not shyly, either: The materials powerhouse says it can produce faster, cheaper, and more complex chips. It aims to be number one or two in a $1 billion domain within five years. Why Corning, why now? Corning parachutes into a biochip playing field of big muscle competitors and flying lawsuits. But with $4.7 billion in 1999 revenues followed strongly this year , it's not about Corningware anymore. The company has morphed from a sleepy glass blower into an advanced materials stronghold. This includes fiber optics, where Corning is the number one fiber optic cable maker ahead of Lucent Technologies (NYSE: LU) Investors have rewarded Corning by quadrupling Corning's stock price in one year. (Drip Port readers recently

58. VetGen - Purebred Animal Genetic (DNA) Disease Testing And Profiling primarily for the purpose of parentage testing and the These tissues contain theDNA which is then extracted CLEAR the defective gene is not present in the http://www.vetgen.com/SCID_article1.html

Avoiding SCID in Arabian Horses by Inge Craik There is a DNA test for Severe Combined Immunodeficiency "SCID" in Arabian Horses. SCID was first reported in Arabian foals in 1973 by McGuire and Poppie Australia . In 1980, Perryman and Torbeck, in the U.S. , showed that SCID in Arabian horses was inherited as an autosomal recessive condition, which means that one copy of the disease gene is inherited from a carrier stallion and another from a carrier mare. The foal which inherits two copies of the disease gene is affected with a lethal inability to fight infections, and dies within the first few months of life. Matings between two clear horses as well as matings between a clear and a carrier horse will NEVER produce an affected animal. By definition, carriers of genes for autosomal recessive disorders are completely free of clinical signs of the disease. That is, carriers do not have any negative consequences to their health or performance. If two carriers are mated, there is a 25% chance that the foal will be clear, 50% chance that it will be a carrier and 25% chance that it will be affected, a chance not worth taking. Prior to the advent of molecular genetic testing for autosomal recessive disorders, the only way an Arabian Horse was identified as carrier was when he or she produced an affected offspring. The traditional recommendation in veterinary medicine would be gelding of these animals to prevent other affected offspring being produced. This is no longer necessary and not in the best interest of the breed. Carrier horses that have desirable traits can now be mated to tested horses that are clear and

59. VetGen - Purebred Animal Genetic (DNA) Disease Testing And Profiling - Epilepsy is expected to lead to new gene discoveries benefiting both therapy in humans andgenetic testing in dogs. VetGen will focus on collecting (dna) sample from http://www.vetgen.com/epilepsy.html

VetGen Awarded Grants from the National Institute of Health and the AKC Canine Health Foundation to Study Canine Hereditary Epilepsy VetGen, the world's leader in veterinary genetic disease research and test development, will focus on discovering new disease genes responsible for hereditary epilepsy in dogs and humans. This research will be funded by a NIH grant entitled "Canine Gene Discovery and Epilepsy Therapy" as well as funds from the AKC Canine Health Foundation. Dr. George Brewer, VetGen's Scientific Director is the Principal Investigator. The goal is to develop a linked gene marker to one or more canine epilepsy genes. Developing such linkages is expected to lead to new gene discoveries benefiting both therapy in humans and genetic testing in dogs. VetGen will focus on collecting samples from families of Australian Shepherds, Beagle, Dalmatian, Collie, English Springer Spaniel, Irish Setter, Shetland Sheepdog, Schipperke, Vizla, in which hereditary epilepsy has been documented. Your help is quickly needed to further this research!

60. DNA Testing For All; Understanding FSHD; GNN Compendium Of Sequenced Genomes; Ve of thalassemia in Mediterranean countries, and his group pioneered novel methodsfor (dna) testing (the now ubiquitous buccal cheek swab) and gene therapy. http://www.bio-itworld.com/archive/bases/082202.html

More Information About Home Archive Around the Bases > DNA Testing for All; Understanding FSHD; GNN Compendium of Sequenced Genomes; Venter's New Foundation DNA Testing for All; Understanding FSHD; GNN Compendium of Sequenced Genomes; Venter's New Foundation By Kevin Davies Editor-in-Chief Aug 22, 2002 FIRST BASE "DNA testing for all" is the provocative title of a commentary by Robert Williamson and Rony Duncan in the 8 August issue of Nature . Calling DNA testing "the most important advance in forensics in our generation, and probably in the whole of human history," Williamson, who is director of the Murdoch Institute in Melbourne, and Duncan argue forcefully that everyone should be subject to DNA testing in the interests of civil liberty. The only fair alternative would be to test nobody. Williamson has an outstanding record in contributing to the societal importance of genetics. During his tenure as chair of biochemistry at St. Mary's Hospital Medical School in London (a stone's throw from the site of Alexander Fleming's discovery of penicillin), his team was seldom out of the limelight during the 1980s, mapping the genes for muscular dystrophy, cystic fibrosis, and many other serious genetic disorders. Williamson was a leading advocate of prenatal diagnosis of thalassemia in Mediterranean countries, and his group pioneered novel methods for DNA testing (the now ubiquitous buccal cheek swab) and gene therapy. DNA testing for all Nature 418, 585-586 (2002).[Subscription required]

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