24 citations
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  July 2017   in “Structure”    FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.  
               49 citations
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  January 2006   in “Developmental Dynamics”    Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.  
     
           12 citations
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  January 2016   in “Endocrinology, diabetes & metabolism case reports”    Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.  
     
           1 citations
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  November 2021   in “Biomedicines”    Understanding how acne develops in different diseases could lead to new treatments.  
               29 citations
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  January 2020   in “Frontiers in endocrinology”    Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.