BillionToOne, Inc., a molecular diagnostics company with a mission to create the most powerful and accurate tests that are accessible to all, announced today the launch of an expanded offering for ...

the first cell-based gene therapy for the treatment of wounds in patients with recessive dystrophic epidermolysis bullosa (RDEB), a serious and debilitating genetic skin disease. There is no cure ...

Zevaskyn is supplied as a single-dose of up to 12 cellular sheets consisting of a patient's own viable, gene-modified cells that contain functional copies of the COL7A1 gene, which express ...

Prademagene zamikeracel (Zevaskyn) is the first and only cell-based gene therapy for wound treatment in patients with recessive dystrophic epidermolysis bullosa. The approval is based on the ...

Please provide your email address to receive an email when new articles are posted on . Recessive dystrophic epidermolysis bullosa is a rare and serious condition. Zevaskyn is the first FDA ...

“Grafting gene-corrected skin onto chronically open wounds of patients with recessive dystrophic epidermolysis bullosa promises the potential to provide long-term healing of wounds, reduction in ...

The signing of Cam Jurgens just days before the NFL Draft is why the Eagles traded C.J. Gardner-Johnson and let several players exit in free agency – to sign young players they drafted in ...

Some variants have no effect while others can cause, for example, autosomal recessive hereditary diseases. People who are called “carriers": have only one variant in only one of the two copies of a ...

There are different ways this can happen. To have a child born with what’s called an “autosomal recessive disease” like sickle cell disease or cystic fibrosis, both you and your partner must ...

He remembers some tragic examples: families who lost several children ... to say that cousin marriage is the root of all excess recessive disorders in Bradford or in Pakistani communities.

Prenatal risk assessment for autosomal recessive diseases can be particularly complex when, for example, only one or no mutation is detectable in the fetus and when mutation detection rates and ...