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The treatment effectively promotes hair regrowth in androgenetic alopecia without causing skin irritation.

Different gene mutations cause different types of ichthyosis, with some new mutations found.

TGF-β2 helps activate hair follicle stem cells by counteracting BMP signals.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

Thymic mesenchymal cells have unique gene expression that supports their specific functions in the thymus.

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

CCL5 is important for the hair growth potential of human dermal papilla cells.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Activated β-catenin affects hair growth and skin thickness, and changes are reversible.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

Overexpressing Tβ4 in cashmere goats improves hair fiber traits and increases cashmere yield.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

PADI4 enzyme slows down cell growth in developing hair follicles.

Removing Mediator 1 from certain mouse cells causes teeth to grow hair instead of enamel.

lncRNA MTC affects protein levels in goat skin cells, impacting hair growth.

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

TGF-alpha affects skin thickness, hair growth, and may contribute to psoriasis and papilloma formation.

The MAGE3 hypothesis for alopecia areata did not lead to a significant breakthrough.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Poncirin is a promising inhibitor of Janus Kinase 3, potentially better than tofacitinib.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Thymus-derived Tregs, not peripherally-derived Tregs, primarily regulate type 1 diabetes in the NOD mouse model.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.