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A genetic marker linked to a type of hair loss was found in most patients studied.

Certain gene changes and hormone levels are linked to female hair loss.

A new gene mutation causes long hair in some Maine Coon cats.

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

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

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

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Four new FGF5 gene variants cause long hair in dogs.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Fgfr2b helps maintain healthy skin and prevent cancer.

The scraggly mutation causes hair loss and skin defects in mice.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

New genetic mutations causing hair loss were found in a Chinese family.

The LTF gene may help predict and manage nonspecific orbital inflammation.

Suppressing very long chain fatty acids is linked to skin cancer.

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

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

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

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

GLI2 increases follistatin production in human skin cells.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.