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AcSDKP may help prevent skin and hair aging and promote their growth.

A standardized consent form for PRP injections improves patient trust and legal protection.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

CircAGK affects cell death in hair cells by controlling the miR-3180-5p/BAX pathway, which can lead to hair loss.

CTP-543 effectively promotes hair regrowth in adults with moderate to severe alopecia areata.

Higher IL-31 levels are linked to worse itching in chronic kidney disease patients.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.

The study found that tight junctions reach the top layer of the skin's stratum granulosum, not just the second top layer as previously thought.

Corin helps control salt and sweat release in sweat glands.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

Keratin 17 is crucial for normal hair growth by regulating hair cycle transitions with TNFα.

Expand access to prevention and address barriers for sex workers in Kostanay.

The 4C32 gene may help in mouse skin development and differentiation.

The study found that specific proteins are markers of hair follicle development in human fetuses.

New genetic mutations linked to rare skin disorders were found in three newborns.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

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Both rosemary extract and 2% ketoconazole lotions effectively treat seborrheic dermatitis and improve quality of life.

AP-1 controls tumor cell type by affecting key signaling pathways.

Acidic keratin genes are on CFA9 and basic keratin genes are on CFA27 in dogs.

A 10-year-old boy recovered from a scalp infection caused by a fungus after treatment with itraconazole.

A specific gene mutation causes different hair defects in Indian monilethrix families.