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MUMBAI, Sept. 29 (Xinhua) -- Indian markets opened higher on Friday.
Equity benchmarks started off October series on a positive note.
The benchmark S&P BSE Sensex opened at 31,379.57 Dede Westbrook Jaguars Jersey , 97.09 points or 0.32 percent up compared to its previous close at 31,282.48.
Large flower terrace gleams on Tian'anmen Square in Beijing
Lanzhou-Chongqing railway to open to traffic on Sept. 29
Ceremonies held around China to celebrate birthday of Confucius
Japanese PM attends ceremony marking China's upcoming National Day
Four pandas from SW China make debut in NE China's Shenyang
Modern manufacturing, transport help six Chinese provinces develop fast
A look at Kantuman Bazaar in China's Xinjiang
Scenery of terraced fields in Houyuan Village Dawuane Smoot Jaguars Jersey , China's Fujian
WASHINGTON， Jan. 11 (Xinhua) -- U.S. researchers have taken an important step toward using the powerful gene editing tool CRISPR-Cas9 to cure a rare genetic immunodeficiency disorder called chronic granulomatous disease (CGD) and perhaps other blood disorders.
Researchers from the U.S National Institute of Allergy and Infectious Diseases (NIAID)， part of the U.S. National Institutes of Health， said Thursday they have successfully harnessed the CRISPR-Cas9 technology to repair the disease-causing mutation in blood-forming stem cells taken from CGD patients.
After transplant into mice， the repaired stem cells developed into normally functioning white blood cells for up to five months， with no signs of side effects， according to their study published in the U.S. journal Science Translational Medicine.
"The most exciting finding in the study was that the gene-repaired stem cells that functioned as normal cells continued to do so after transplant into mice， indicating gene correction of long-term engrafting primitive stem cells，" the researchers said in a statement.
"This is one finding that provides hope that this can be further developed into a clinical treatment in the future."
CGD is caused by mutations in the gene CYBB， which provides instructions for production of a protein called NOX2.
Defects in NOX2 impair the infection-fighting ability of white blood cells， leaving people with CGD highly susceptible to life-threatening infections.
While stem cell transplantation offers a potential therapy for CGD， the procedure carries a risk of toxicity and potentially lethal complications.
In the new study， NIAID researchers focused on a CYBB mutation in which a single change in the genetic code leads to production of inactive NOX2.
The investigators used CRISPR-Cas9 to specifically target .