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Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

A new method helps understand hair shine and various products improve hair care.

SIRT7 protein is crucial for starting hair growth in mice.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

Targeting immune pathways like JAK/STAT may help treat frontal fibrosing alopecia.

A mutation in the KRT74 gene causes tightly curled hair.

FFA is more common in postmenopausal women, can affect younger women, and may stabilize over time.

Human hair and skin friction vary by ethnicity, hair type, and environmental conditions.

Most patients with frontal fibrosing alopecia are middle-aged women, often have thyroid disease, and some treatments can help stabilize the condition.

F4 and F6 hair gels showed promise for improving hair care but need more testing.

Being allergic to linalool, a common fragrance ingredient, might contribute to developing frontal fibrosing alopecia.

Friction causes hair breakage during combing, and fragment count predicts hair strength.

Shampoo B, which uses water-soluble silicone, is better at detangling hair in wet conditions due to its two-layer conditioning film.

Polyquaternium-7 improves hair condition.

Hair fibers interact through classical forces, which are influenced by treatments and products, important for hair care and other applications.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

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

Hair treatments like bleaching increase friction by exposing tiny pores on the hair surface.

The study found that hair fragility in Pili annulati may be caused by cavities and damage within the hair shafts.

Using a hot iron on wet hair can cause dry, brittle hair with air bubbles inside.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

Two siblings have a rare hair condition caused by a new genetic variant.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.