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A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

A specific gene mutation causes sparse, brittle hair in a family.

A new staining method helps tell growing from resting hairs to diagnose hair loss.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Lack of Crif1 in hair follicle stem cells slows down hair growth in mice.

Vitamin D Receptor is crucial for hair follicle shrinkage and cell death, affecting hair growth.

Diphencyprone (DPC) is an effective and safe long-term treatment for alopecia areata, especially with maintenance therapy.

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Hair growth and shedding involve specific cell changes and gene roles.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

A new method helps detect androgen receptor movement in cells, aiding research on hair loss treatments.

The method allows precise cell removal without harming nearby tissues.

Mouse hair follicle cells briefly grow during the early hair growth phase, showing that these cells are important for starting the hair cycle.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

Dicer is crucial for hair growth in mice.

Ambras syndrome's genetic cause is unknown, as it isn't linked to androgen levels.

Deucravacitinib did not significantly improve hair regrowth in alopecia areata patients.

Deucravacitinib helped regrow hair and reduce plaques in a woman with discoid lupus erythematosus without side effects.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

A new genetic mutation was found causing hair and eye issues in a boy.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.