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Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

A specific genetic variation affects wool quality in sheep.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

Mutations in the hairless protein gene cause hair loss.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

cDermo-1 causes dense skin, feathers, and scales in chickens.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Overexpressing Tβ4 in cashmere goats improves hair fiber traits and increases cashmere yield.

p2y5, now called LPA6, is a receptor important for human hair growth.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

Potential new drugs for treating PCOS were identified.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

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

Syntaxin 9 helps in transporting and signaling of the EGF receptor in skin and stomach cells.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Key genes affect cashmere quality differences between Jiangnan and Changthangi goats.

Spt4 and Spt6 are essential for fat cell development.

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

LHX2 is crucial for development, tissue repair, and preventing diseases.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.