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Desmopressin-loaded liposomes can effectively deliver drugs through the skin, improving bioavailability and patient compliance.

Targeting the PIEZO1 and MLCK axis may offer a new treatment for hair loss.

Antisense oligonucleotides can reduce androgen receptor levels in skin cells, suggesting potential for treating skin disorders.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

N‐AOHPA is a promising alternative to traditional surfactants for better hair conditioning.

Increased K+ permeability alone may not promote hair growth.

Dermal EZH2 controls skin cell development and hair growth in mice.

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

A peptide known for reducing wrinkles also effectively inhibits an enzyme linked to skin inflammation and acne.

Targeting the PGD2-DP2 pathway may help treat hair loss.

Pyrene excimer nucleic acid probes are promising for detecting biomolecules accurately with potential for biological research and drug screening.

A peptide from hair follicle stem cells promotes hair growth by activating specific skin cells.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

A new gene mutation causes a rare type of hair loss.

Quercetin and kaempferol may be effective and safe natural treatments for hair loss.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

AtVPS29 is essential for proper plant growth by regulating gibberellin signaling.

Researchers developed reliable models to predict how well certain compounds bind to androgen receptors, emphasizing the importance of atomic electronegativity.

New compounds called benzoquinolinones may treat conditions linked to excess DHT.

A specific DNA region controls skin cell gene expression by working with certain proteins.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Minoxidil's absorption is too variable for it to be a reliable reference drug.

Major histocompatibility antigens are found in specific skin cells and structures, but not in sweat glands.

Inflammation damages sweat ducts, causing sweat gland injury.

Neuronatin is found in various cells of rat tissues and has a unique location in sperm cells.