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Substances from human hair cells can affect hair loss-related genes, potentially leading to new treatments for baldness.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

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

The study found potential new DNA patterns in fertility genes, but further testing is needed.

The Gsdma3 gene is essential for normal hair development in mice.

Follistatin helps hair growth and cycling, while activin prevents it.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

NFIB and STAT5 work together to control specific genetic programs in cells.

EGF and EGFR are important for goat skin development, increasing from weeks 6 to 21.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

The gene GJA1 is important for regulating coarse hair density in goats.

FOXC1 boosts SFRP1 in hair loss, suggesting new treatments.

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.

FOL-005 peptide can reduce human hair growth by lowering FGF7 levels.

Increased PHGDH expression causes early melanin buildup in hair follicles.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

PIKFyve is essential for normal platelet function and its deficiency causes organ issues and macrophage infiltration.

Researchers found specific genes in the part of hair follicles that could help treat hair disorders.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

EGF–FGF2 helps mouse stem cells grow and become more like nerve cells.

TGF-β signaling is essential for new hair growth after a wound.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

FGFR2 signaling controls Merkel cell formation in different skin regions.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Gsdma3 affects hair growth by controlling Wnt5a, which influences hair cell development.

CGF therapy may effectively treat psoriasis by reducing inflammation.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

A new method helps grow skin stem cells better, which could improve skin grafts for burn victims.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.