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

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

A gene mutation in Lama3 is linked to a common type of hair loss.

AR gene not major factor in female hair loss; different from male hair loss.

Higher levels of IL-1a and IL-1RA were found in severe alopecia areata cases.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

CD117 and platelet-derived growth factor receptor α may play a role in alopecia areata.

High levels of HSP70 and IL-15 are linked to more severe alopecia areata.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

Researchers found certain genes are overactive and others are underactive in men with early balding, which could help create new treatments.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

EDA2R is a key gene linked to ageing and diseases, and targeting it may help treat conditions like hair loss and chronic diseases.

Alopecia areata involves persistent gene abnormalities and immune activity, even in regrown hair, suggesting a risk of relapse.

hsa_circ_0001079 may help diagnose and treat hair loss.

A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

TH antibodies in vitiligo and AA patients recognize the same protein parts.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

CD4 T cells need IFN-γ to cause hair loss in alopecia areata.

Higher CRHR1 levels in AA patients lead to increased inflammation.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Increased HIF-1α is linked to the inflammation and severity of hidradenitis suppurativa, suggesting treatments that lower HIF-1α could help.

Farudodstat may help treat alopecia areata by protecting hair follicles.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

Hydroxytyrosol may help treat hair loss by reducing inflammation and oxidative stress.

Higher LDL cholesterol may increase the risk of hair loss, while HDL cholesterol does not.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

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

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.