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

The research found new potential mechanisms in mouse hair growth by studying RNA interactions.

Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Early detection and treatment of Menkes disease with copper injections are crucial for better outcomes.

Mitochondrial Complex I reduces inflammation and increases bone breakdown by affecting certain immune cells.

miR‑339‑5p can slow down hair follicle stem cell differentiation by targeting DLX5.

Certain microRNAs may protect against hair loss in alopecia areata and could be potential treatment targets.

The LAMTOR3 gene is involved in cashmere goat hair growth and is affected by certain treatments and other genes.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

hsa-miR-193a-5p may help diagnose and treat alopecia areata.

No clear link between specific gene and hair loss in Mexican brothers.

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

Targeting mitophagy may help treat alopecia areata by reducing inflammasome activation.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.

MPZL3 protein affects hair growth cycles and could help manage hair loss.

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

Pili annulati is caused by a protein metabolism disorder affecting hair structure.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

miRNA-211 reduces melanin in Cashmere goats by suppressing AP1S2.

Double-stranded RNA causes inflammation in hair follicle cells, which may help understand and treat alopecia areata.

Glutamic acid microneedle patches promote better hair growth than traditional treatments.

PAON shows skin patterns due to genetic mosaicism.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.