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Fadrozole and finasteride change gene expression related to sex hormones and thyroid hormones in frog larvae development.

BTNL2 helps protect hair follicles from immune attacks.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

FGFR2 signaling controls Merkel cell formation in different skin regions.

TGF-β3 controls stem cell growth and development, varying by cell type and conditions.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

GFP transgenic mice help study cell origins in skin grafts.

The N-K GM Series offers a new method to reduce aflatoxin poisoning and cancer, improving health and saving costs in affected regions.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

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Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

The mutation causing Hutchinson-Gilford progeria syndrome leads to severe skin problems and early death in mice.

The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

TGF-β inhibitors may help treat liver fibrosis by targeting various pathways.

Tofacitinib may help treat nail dystrophy, especially when other treatments fail.

The assay effectively identifies compounds that affect immune cell activation.

Fecal microbiota transplantation effectively reduces symptoms of Feline Hyperesthesia Syndrome in cats.

Endoglin is crucial for proper hair growth cycles and stem cell activation in mice.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

Reducing IGF-1 can help rejuvenate hair follicles and prevent hair graying and loss.

The combination of tadalafil and finasteride improves urinary symptoms and erectile function in men with enlarged prostates.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

An intact skin barrier is crucial to prevent infection in cases of tether-induced tenosynovitis.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Fz3 and Fz6 can partially replace each other in tissue polarity and axon guidance.

Tanshinone IIA helps protect skin tissue from low oxygen damage by boosting certain cell markers.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

The B2C promoter works in sheep cells but not in mouse embryos.