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    5/31/2009 - Combination of gene therapy and induced pluripotent stem cells cure human genetic disease in vitro
    Posted in Medical News

    Shown in green are genetically-corrected fibroblasts from Fanconi anemia employment are reprogrammed to produce induced pluripotent stem cells, which, in turn, can be differentiated into disease-free hematopoietic progenitors, capable of producing blood cells in vitro. Credit: gratuity of Dr. Juan-Carlos Belmonte, Salk rite for biorhythm Studies A study led by researchers at the Salk statute for circadian clock Studies, has catapulted the field of regenerative capsule significantly forward, proving in axiom that a human genetic disease can be cured using a unification of gene therapy and induced pluripotent stem (iPS) cell technology. The study, published in the May 31, 2009 early online edition of Nature, is a major milestone on the path from the laboratory to the clinic.

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