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Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Specific keratin gene mutations can cause monilethrix.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

Mutations in the hairless gene cause a rare form of permanent hair loss.

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

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

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

NKG2D+CD4+ T cells are higher in alopecia areata patients and may be involved in the disease.

hHbl gene is active in hair shaft cells and some pilomatricomas.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

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

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

LHX2, with other markers, can identify hair placodes in rats.