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Researchers found WNT10A to be a key gene in developing goat hair follicles.

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

The study found key long non-coding RNAs involved in yak hair growth cycles.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Accurate diagnosis and early specialist referral are crucial for managing 46,XY Disorders of Sex Development.

CDP is crucial for lung and hair follicle cell development.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

CNVs influence hair length in Tianzhu white yaks.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Mutations in the LIPH gene cause woolly hair in a child.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

TGF-beta 1 and IGF-II mRNA have specific patterns in pig subcutaneous tissue, affecting fat and muscle development.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

miR-144-y and FOXO3 play key roles in skin and feather development in Zhedong White geese.

A genetic variant in goats is linked to cashmere growth.