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A new DSG4 gene mutation causes hair defects in a young girl.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

A new gene mutation causes insulin resistance in a girl and her mother.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

Mutant stem cells adapt their metabolism differently to outcompete normal cells in the skin.

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

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

Changes in KRT17 gene activity linked to wool production in Angora rabbits.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

FGF5 gene mutations cause long hair in domestic cats.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

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

A missing mK6irs1 gene causes hair loss in mice.

A specific mutation in Kras causes abnormal tissue changes by making a cell signal continuously active, which disrupts normal cell coordination.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

DKK4 can be used to improve wool quality in Zhexi Angora rabbits.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Using special RNA to target a mutant gene fixed hair problems in mice.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

KAP8.1 gene variations affect cashmere weight in Inner Mongolian goats.

Removing β-catenin in certain stem cells causes hair whitening and pigmentation issues.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.