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Genetics

New syndrome named, causes a rare intellectual disability

Pediatric researchers, using high-speed DNA sequencing tools, have identified a new syndrome that causes intellectual disability (ID). Drawing on knowledge of the causative gene mutation, the scientists' cell studies suggest ...

Medical research

Gene variants found to strongly improve bone density in girls

Pediatric researchers have found that rare genetic changes strongly increase the likelihood that a child will have higher bone density, but only in girls. Because childhood and adolescence are critical periods for bone formation, ...

Genetics

New gene variants found in childhood body mass index

An international team of scientists has identified novel gene locations associated with childhood body mass index (BMI)—an important measurement related to childhood obesity. The meta-analysis, covering over 47,000 children, ...

Oncology & Cancer

Younger T cells may improve immunotherapy for children's cancer

Pediatric oncologists from The Children's Hospital of Philadelphia (CHOP) have investigated techniques to improve and broaden a novel personalized cell therapy to treat children with cancer. The researchers say that a patient's ...

Medical research

Gene therapy for rare bleeding disorder achieves proof-of-concept

Hematology researchers have used a single injection of gene therapy to correct a rare bleeding disorder, factor VII deficiency, in dogs. This success in large animals holds considerable potential for a safe, effective and ...

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