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The arrector pili muscle attaches to the extracellular matrix using α5β1 integrin and connects muscle cells using α1β1 integrin.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

PAD type III enzyme is specific to rat skin and hair follicles.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

The fuzzy gene is crucial for controlling hair growth cycles.

Targeting the narrowest part of the anterior chamber angle may help prevent pupil block in glaucoma.

A 6-year-old boy's skin condition improved after stopping a specific treatment and starting new medications.

Specific mutations in a receptor cause facial abnormalities and hair loss.

ARHGEF3 is essential for proper hair follicle development.

The ABHRS held a test in Capri, Italy.

A20 protein is crucial for normal skin and hair development.

AcD scaffolds improve tissue repair and regeneration by combining stem cells with a supportive matrix.

People with Alopecia areata have higher levels of certain T regulatory cells in their blood.

α3β1 integrin is essential for skin stability and proper wound healing.

Hair loss improved with treatment and successful transplant.

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.

Avicequinone C, a compound found in the Avicennia marina plant, can reduce hair loss by inhibiting a hormone linked to androgenic alopecia.

The method can measure vitamin B3 levels in human hair accurately.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

The document concludes that doctors should recognize congenital triangular alopecia to avoid unnecessary treatments, as it does not respond to steroids like alopecia areata does.

KSR1 is crucial for certain skin tumor formation and could be a cancer therapy target.

CDH3-related disease causes worsening eye and hair issues.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

Stopping S100A3 activity slows down hair growth in mice.