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MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

Radiation significantly slows down wound healing in mice.

Certain changes in the KAP6-1 gene affect the thickness and length of cashmere goat fibers.

FGF signaling is crucial for starting feather development in chicken embryos.

Zebrafish helped find new ways to prevent drug-induced hair cell death and potential treatments for hearing loss.

PROTAC technology shows promise for cancer treatment but needs more effective E3 ligase recruiters.

Stem cells control their future role by changing ERK signal timing, affecting tissue regeneration and cancer.

Alopecia Areata can develop without perforin-mediated cytolysis.

The study concluded that the developed models are effective for studying hair growth mechanisms and testing new treatments.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

FGF5 gene mutations cause long hair in domestic cats.

Abnormal keratin expression in mice causes severe oral issues, affecting feeding.

A compound from Calophyllum inophyllum L. leaf may help treat non-small cell lung cancer.

High-throughput LC-MS screening is effective for finding new autotaxin inhibitors for asthma treatment.

Akt2 protein is essential for normal cell division in early mouse embryos.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

The new rodent model successfully mimics non-lean human PCOS symptoms.

Wedelolactone selectively kills prostate cancer cells without harming normal cells.

The research suggests that immune cells and a specific type of cell death called ferroptosis are involved in Frontal fibrosis alopecia.

Blocking casein kinase 1 in skin cells can help melanocyte precursors move better, potentially helping with conditions like vitiligo or gray hair.

A mutation in the Sgkl gene causes defective hair growth in mice.

RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

Kremen is crucial for proper development and preventing tumors by regulating Wnt signaling.

K10 may not prevent tumors as previously thought and might increase benign tumor risk.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

The model effectively mimics radiation-induced skin damage for future research.

A missing mK6irs1 gene causes hair loss in mice.

HOXC13 is essential for hair and nail development by regulating Foxn1.