Unanticipated findings cast new light on the genetic regulation of different brain tumors
The findings highlight the importance of considering the mechanisms of gene regulation involved in different tumors when planning therapies.
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Sox9 reshapes the biliary tree in Alagille syndrome
Alagille syndrome is a rare pediatric genetic disorder that can affect the liver, heart, kidneys, blood vessels, skeleton and other tissues. One major characteristic of
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No SOX9, no cartilage; and how DDRGK1 causes a rare human skeletal dysplasia
SEMD, Shohat-type spondyloepimetaphyseal dysplasia, is a rare type of skeletal dysplasia that affects the development of cartilage and results in a form of dwarfism with a
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