Video about an 8 year old boy who is the first to get gene therapy for muscular dystrophy.
Archive for November, 2008
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A stem cell is a cell that has the ability to develop into any type of tissue or cell in the body.Embryonic stem cells have the ability to transform into any specific tissue or cell for example, bone marrow. Adult stem cells act as a repair system for the body by regenerating tissues and cells such as blood and skin tissue.
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PKU is a genetic disorder caused by an enzyme deficeincy on chromosome 12. Individuals with this disorder are unable to process an amino acid found in food, which builds up in the blood. This build up can cause seizures and problems with brain development.
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Chavonne Jones talks about genetics education awareness by blogging and posting videos on HumanGeneticsDisorders.Com
NSGC Conference exibit and MBA thesis poster presentation videos from the October 24-28 2008 AEC Conference by Chavonne Jones
HUMAN GENETICS
Chavonne Jones presents Cri du Chat Syndrome at Human Genetics Disorders
Chavonne Jones presents Cri du Chat Syndrome Video at Human Genetics Disorders
Chavonne Jones presents Cri du Chat Video-European Rare Disease Day 2008 at Human Genetics Disorders
Advanced Parental Age and the Risk of Autism Spectrum Disorder-American Journal of Epidemiology
Type 1 diabetes: good genes behaving badly
Genomicron: Pellionisz Google Tech presentation.
Sandwalk: Evolution by Gene Duplication
The Full mtDNA Genome of Ötzi is Sequenced (Twice?) » The Genetic Genealogist
PERSONALIZED GENETICS
How Many Ways Can A Physician Be Sued (Over Genetic Tests)?
Gene Sherpas: Personalized Medicine and You: Genetic Test or Family History? Which Matters More?
Asking hard questions about personal genome
Who’s first? Happy First Birthday, commercial personal genomics! « Pimm - Partial immortalization
The Navigator - Navigenics Blog - Genes are at the heart of a new journal
That concludes this edition. Submit your blog article to the next edition of gene genie using our carnival submission form.
Past post and future hosts can be found on our blog carnival index page.
Video from European Rare Disease Day 2008 talks about Cri Du Chat Syndrome
A video by Jordan Stoltzfus about Cri du Chat Syndrome
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Cri-du-Chat Syndrome is a rare genetic disorder caused by a partial deletion on chromosome 5. Infants born with this disorder have kitten-like crying sounds do to larynx and nervous system problems. Individuals with this disorder may have symptoms such as; feeding problems due to swallowing and sucking difficulties, low birth weight, constipation, behavioral problems, hyperactivity, and severe cognitive, speech, and motor delays.
Claudette brief shares her experiences with living with sickle cell anemia.
Amanda Watermeier shares her story about over coming Wilson’s Disease.