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Dendrobium officinale polysaccharide helps hair regrowth in hair loss mice by affecting local steroid metabolism and hair follicle responses.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

Phospholipase C-δ1 is crucial for normal hair development.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

A low dose of rapamycin increases inner ear hair cell creation by boosting SOX2+ cell numbers.

Finasteride crystals are held together by hydrogen bonds and weak interactions, forming synthon pseudopolymorphs.

Different types of androgens bind differently to two receptors, AR1 and AR2, in Atlantic croaker's brain and ovarian tissues, suggesting these receptors may control different androgen actions in fish.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

Mouse keratin 6 isoforms have different expression patterns in various tissues.

ROXY proteins help plants respond to nitrate shortage by affecting nutrient sensing and growth.

Microspheric skin organoids can be used for drug testing, identifying Minoxidil as a Wnt pathway activator.

RORA boosts autophagy in hair follicle stem cells, potentially aiding hair growth.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Polyamines are important for hair growth, but more research is needed to understand their functions and treatment potential.

Restoring EDA and WNT pathways early may help improve skin, hair, and teeth issues in hypohidrotic ectodermal dysplasia.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Lateral plate mesoderm helps create skin and amnion-like tissues for studying development and therapies.

Oxytocin from hair cells helps hair growth and stem cell increase.

New steroidal compounds moderately block an enzyme related to testosterone conversion, less effectively than finasteride.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

μ-Crystallin may help hair growth by affecting thyroid hormone levels in mouse hair follicles.

S100A8 and S100A9 proteins help form hair shafts during growth.

Flightless I protein affects hair growth, with low levels delaying it and high levels increasing hair length in rodents.

AtCSLD3 and GhCSLD3 genes enhance root growth and cell elongation in plants.