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Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

The plant extract mixture improves skin health by reducing inflammation, boosting collagen, and supporting anti-aging.

A mutation in the KRT74 gene causes tightly curled hair.

A rare gene variant causes hair and nail issues in a family.

A new mouse mutation causes skin and hair defects due to a gene change.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

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

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

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

KRT85 gene variations can help improve wool traits in sheep through selective breeding.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Two genetic variations in Moa buffalo help them adapt to heat.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

KRT71 gene variants may influence camel hair shape but don't fully explain it.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

A specific gene variant may increase the risk of developing Alopecia Areata.