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Four genes are potential markers for hair loss condition alopecia areata, linked to a specific type of cell death.

A mutation in the human hairless gene causes alopecia universalis.

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

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Injecting specific oligonucleotides can change hair growth and structure by altering a gene.

Mutations in the HOXC13 gene cause hair and nail development issues.

The study suggests that changes in immune system receptors and their interaction with a cell component may be important in the development of a type of hair loss condition.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

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

CT60 polymorphism might increase the risk of Alopecia Areata.

Linalool in fragrances may harm hair follicles and contribute to hair loss.

A mutation in mice causes hair loss and immune problems.

FoxN1 overexpression in young mice harms immune cell and skin development.

5% topical minoxidil improves hair density and quality in monilethrix patients.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

Being allergic to linalool, a common fragrance ingredient, might contribute to developing frontal fibrosing alopecia.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

A new gene mutation causes a rare type of hair loss.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

A 2-year-old girl had a hair disorder not shared by her identical twin.

Cathepsin L deficiency causes hair and skin issues in mice.

A specific gene mutation causes different hair defects in Indian monilethrix families.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

New genes linked to male pattern baldness were found on chromosome 20p11.

Frontal fibrosing alopecia can occur in children, not just postmenopausal women.

TRPV3 gene mutations cause Olmsted syndrome symptoms, but severity varies.

15-lipoxygenase helps keep skin healthy by reducing inflammation.