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Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Keratin 79 marks a new group of cells that are key for creating and repairing the hair follicle's structure.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

A blood pressure drug, diltiazem, may also help treat influenza.

Researchers found a new mutation causing total hair loss from birth.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Found new possible treatments for hair loss.

S5αR inhibitors might help treat schizophrenia and other mental disorders but need more research.

Researchers found 15 new genetic links to skin traits in Japanese women.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

No FDA-approved treatments for chemotherapy-induced hair loss existed in 2006; more research was needed.

A specific genetic deletion in goats affects cashmere yield and thickness.

Animal models have helped understand hair loss from alopecia areata and find new treatments.

Genomic approach finds new possible treatments for hair loss.

Men are more likely to have severe respiratory viral infections like COVID-19 due to hormonal and genetic differences, while women generally have stronger immune responses.

Aquaporins could be new drug targets for treating polycystic ovary syndrome.

New treatments targeting skin stem cells show promise for skin repair, anti-aging, and cancer therapy.

Finasteride may affect PNMT, causing side effects.

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

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

HLA-DRB5 and other genes may be linked to alopecia universalis.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

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

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.