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The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

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

VILLIN4 helps root hair growth by organizing actin with calcium.

A gene mutation in Lama3 is linked to a common type of hair loss.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Hair loss gene found on chromosome 3q26.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

A new gene mutation causes a rare type of hair loss.

ARHGEF3 is essential for proper hair follicle development in mice.

CCL5 is important for the hair growth potential of human dermal papilla cells.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

The CD4 protein may play a role in the behavior of certain skin cells, affecting their growth, movement, and differentiation.

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

ALX4 is crucial for normal craniofacial and hair development, with specific roles in different cell types.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

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

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

pCLCA2 protein may help maintain skin structure and function.

A specific gene variant may increase the risk of developing Alopecia Areata.

Overexpression of the HE4 gene in mice causes eye inflammation and cloudiness.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

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