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Molly Portland, Oregon
In early 2005, I was 28 years old and just beginning to break into a career as an opera singer.... More
Hello! I am so excited to be a part of Healthblogger. My son, Benjamin, was born with Cystic... More
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Married my husband Jason, 7/7/2007.  Together we have two children.  Nathan was born... More

f508 mutation Blogs and DiscussionsArticles

 
Ethnicity and Common Mutations by Lauren B. Patient Expert that certain CFTR mutations are more commonly associated with specific races and ethnicities. They have identified 24 mutations, all of which have become part of carrier screening as recommended by the American...
Human p53 Mutations and a Genetic System in Yeast for Functional Identification of Human p53 Mutations by nih.gov with neoplastic transformation. p53 is mutated in about 50% of all human tumors and more than 80% of these mutations are missense, leading to single amino acid changes. This invention relates to human p53 mutants...
ERBB4 Mutations Mutation Identified in Human Melanoma Metastasis Cell Lines (2690, 2379, 2197, 2183, 2535, 2645, 1770, 2359, 223 by nih.gov (also called HER4). These mutations were found to increase the sensitivity of cells in which they reside... that harbor ERBB4 mutations. These cell lines provide methods of identifying specific inhibitors to ERBB4...
Autism, De Novo Genetic Mutation and Environmental Mutagens by Harold L D. Patient Expert by the references to genetic mutations and de novo genetic mutations. I tried to Google my way to a basic... factors can play a role in some genetic mutations: Gene mutations occur in two ways...
Somatic mutations in cancer and genetic syndromes by Dr. Ramunas J. Medical Doctor As for clinical geneticist, traditionally concerned more with germline (hereditary) mutations and disease, it might be strange to search through somatic mutation (or acquired) databases. But it is obvious...
Taking Lessons from the CCR5Δ32 Mutation for Patient Treatment by Dave W. Doctor of PhilosophyHealth Maven mutation, which produces a shortened, nonfunctional protein that cannot act as a coreceptor due to the fact that it is no longer expressed on the cell membrane. Thus, individuals homozygous for the CCR5 mutation (also known...
Scripps Research Answer the Mystery of How Genetic Mutations Lead to Diabetes Type 1 by Medical Quack Patient ExpertHealth Maven mutations for diabetes as mentioned below are published in the Journal of Clinical Investigations.  BD... an answer to the 40-year-old mystery of how certain genetic mutations lead to Type 1 diabetes. This new...
Reassessing the role of mitochondrial DNA mutations in autism spectrum disorder. by Kev Leitch Healthy Living ProfessionalHealth Maven : are there mutations in the mtDNA which increase the risk of autism? A new paper takes a look at the question. They studied 148 patients with ASD and found, well, no support for a link to mtDNA mutations. Here is the abstract...
Genetic Mutations and Nurigenomics: Nutrition for Genetic Disorders at Healthy Being Wellness Center in St. Petersburg Fl 33702 by Melissa G. Patient ExpertComplimentary & Alternative Medicine are caused by genetic mutations and genetic duplications. Commonly known genetic disorders include: cystic... with an enzyme deficiency caused by mutations in a particular enzyme interaction cannot metabolize foods...
IDH1 Mutations in Oligodendrogliomas: PNA-clamping PCR is best analytic method by Dr. Brian M. Medical DoctorHealth Maven Pathology Although direct sequencing of mutations in isocitrate dehydrogenase 1 (IDH1) has been considered to be the gold standard method to detect this mutation, the sensitivity of this technique has been questioned...

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Causes Genetic mutation Acute leukemia begin ... » Read on
Causes Genetic mutation Chronic leukemia beg ... » Read on