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Four genes are potential markers for hair loss condition alopecia areata, linked to a specific type of cell death.

Variants on chromosome 10 affect hair thickness in Dazu black goats.

The SOSTDC1 gene is crucial for determining sheep wool type.

Genetic marker rs12558842 strongly linked to male hair loss.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Alopecia areata involves persistent gene abnormalities and immune activity, even in regrown hair, suggesting a risk of relapse.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

CD99 is highly present in certain skin cells and could help treat skin conditions.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Deleting part of a gene in mice causes wavy hair and high pup loss.

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

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

A20 protein is crucial for normal skin and hair development.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

hsa_circ_0001079 may help diagnose and treat hair loss.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Certain RNAs may help diagnose alopecia areata by affecting keratin genes.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Black women with CCCA are more likely to have uterine fibroids.

The Eda gene helps regulate the hair cycle in goats.

A new mutation in mice causes crooked whiskers and messy hair.

The ASIP gene is crucial for determining cattle coat color.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

S100A3 protein is crucial for hair shaft formation in mice.

KRT72 gene helps form hair.

SLC3A2 is crucial for hair follicle stem cell function and hair growth.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.