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The nanohybrid system significantly improved wound healing and showed strong antibacterial activity.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

Activating Notch in adult skin causes T cells and neural crest cells to gather, leading to skin issues.

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

Crataegus pinnatifida extract may help increase hair growth and thickness in mice.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

Cells treated with Wnt-10b can grow hair after being transplanted into mice.

The tropical legume Sesbania rostrata can form nodules in waterlogged conditions using a different method that involves plant hormones and specific genes.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

Researchers found a new mutation causing total hair loss from birth.

The osteopontin gene is active in a specific part of rat hair follicles during a certain hair growth phase and might affect hair cycle and diseases.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Finasteride side effects in young men may be linked to specific gene variations.

A gene mutation causes woolly hair in a Syrian patient.

The enzyme type 1 5α-reductase is more active in the hair follicle's lower part than in the skin's outer layer.

Some synthetic carbohydrate receptors, especially compounds 3 and 15, show strong potential for treating Zika virus.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A gene called BMAL1 plays a role in controlling hair growth.

MC4R gene variants not linked to female hair loss.

Certain gene variations are linked to better memory in healthy Chinese women.

Mutation in hairless gene may increase hair loss risk.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Finasteride affects SRD5A2 gene pattern, possibly causing lasting side effects.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.