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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

GLI1 RNA CISH effectively identifies basal cell carcinoma but is less specific for benign follicular tumors.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

BST2 protein and certain T cells increase in early alopecia areata.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

HAPLN1 can promote hair growth and may help treat hair loss.

BI 2536 had limited effectiveness against several advanced cancers and caused significant side effects.

Lack of functional CYLD in mice leads to early aging and cancer.

Erythropoietin overexpression disrupts hair growth and fat formation in mice.

The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

Mutations in the DSG4 gene cause specific hair and scalp issues.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

Grafted human scalp samples on mice can produce human hair, useful for studying hair genetics.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

The 2012 criteria are better for diagnosing atypical lupus cases.

Basal cell carcinomas in mice can start from hair follicle stem cells and other skin cell types, depending on signaling levels.

BMP2 and BMPR-IA may stop hair growth while Noggin may encourage it in yak skin.

More research is needed to effectively measure how well GHK–Cu in liposomes penetrates the skin.

TGM3 is important for skin and hair structure and may help diagnose cancer.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

Human scalp hair follicles can produce hormones and have a system similar to a brain-body communication network.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Some hair proteins are specific to hair, while others are also found in skin cells.

Keratin structure changes during keratinization, but the exact model remains uncertain.