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Genetic Link to Schizophrenia Discovered

Sue Wu submitted, created time 8 months 3 days (sciencenow.sciencemag.org)

Researchers have found that people with schizophrenia are far more likely than other people to have a certain type of error in their genes. Scientists believe the finding will help them develop new treatments for schizophrenia and identify young people at high risk of developing the disorder.

6

Good News: Stem Cells Overpower Muscle Disease

Eric wu submitted, created time 11 months 2 weeks (sciencenow.sciencemag.org)

The recent breakthrough of skin cells reprogrammed to behave like embryonic stem cells has stolen the spotlight (ScienceNOW, 6 December), but adult stem cells are proving that they have advantages of their own. In the 13 December issue of Cell Stem Cell, researchers report using stem cells from patients afflicted with a form of muscular dystrophy to correct the disorder in mice. The results suggest that this strategy could one day treat muscular dystrophy in humans as well as other genetic disorders.

5

Newborns Tested for Genectic Disorders

Reviver submitted, created time 1 year 4 months (www.intelihealth.com)

Good news for the nation's babies: Nearly 90 percent of newborns are getting tested for a host of rare but devastating genetic disorders.

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Eating disorders may disrupt menstruation

DanyC submitted, created time 1 year 4 months (www.reutershealth.com)

Any type of eating disorder can boost a woman's likelihood of having irregular menstrual periods, a new study confirms.

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Genetic disorders implicate a human phenome-interactome network of protein complexes

psychologist submitted, created time 1 year 8 months (www.nature.com)

A systematic, large-scale analysis of human protein complexes are performed comprising gene products implicated in many different categories of human disease to create a phenome-interactome network. It was done by integrating quality-controlled interactions of human proteins with a validated, computationally derived phenotype similarity score, permitting identification of previously unknown complexes likely to be associated with disease

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