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research Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization

24 citations , 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.

research Effect of Lentivirus-Mediated miR-182 Targeting FGF9 on Hallux Valgus

4 citations , January 2021 in “International Journal of Medical Sciences”

miR-182 may help treat hallux valgus by targeting FGF9.

research The Noggin Null Mouse Phenotype Is Strain Dependent and Haploinsufficiency Leads to Skeletal Defects

49 citations , January 2006 in “Developmental Dynamics”

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

research Testosterone Replacement in 49,XXXXY Syndrome: Andrological, Metabolic, and Neurological Aspects

12 citations , January 2016 in “Endocrinology, diabetes & metabolism case reports”

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

research Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome

April 2019 in “Journal of the Endocrine Society”

Mosaic Klinefelter syndrome can affect male fertility and may be missed in routine tests.

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