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Progesterone byproduct 5αP stimulates mammary tumor growth, but finasteride can suppress it.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

New mutations in the hairless gene may cause hair loss and affect bone development.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

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.

The research identified new skin traits in mice, some linked to human skin conditions.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

LGR5 is a marker found in hair follicle stem cells in various species and is important for hair growth and skin repair.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

RXR agonists may promote hair growth in humans.

Certain genetic markers can indicate a person's risk of developing prostate cancer.

Dupilumab effectively treats severe skin issues in a rare genetic disorder.

Increased ornithine decarboxylase makes normally tumor-resistant mice more sensitive to tumors.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

MOF controls skin development by regulating genes for mitochondria and cilia.

TBX3 gene affects horse coat color, with higher expression in darker areas.

Blocking a protein called prostaglandin D2 might help treat hair loss.

Chromosomal differences affect how muscle cells respond to testosterone.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Certain variations in the vitamin D receptor gene are linked to an increased risk of polycystic ovary syndrome.

p63 controls Satb1 to help skin develop properly.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

ELL is crucial for gene transcription related to skin cell growth.