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The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Arg1+ macrophages may play a role in Alopecia Areata, offering new treatment targets.

Two new gene clusters important for hair formation were found on human chromosome 11.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

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

Upadacitinib effectively improved severe atopic dermatitis and alopecia universalis in a 29-year-old man.

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

AP-1 controls tumor cell type by affecting key signaling pathways.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

Two new gene clusters important for hair formation were found on human chromosome 11.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

ACBP is crucial for healthy skin in mice.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

A new gene mutation causes insulin resistance in a girl and her mother.

AXR3 and SHY2 genes control the growth and timing of root hair development in plants.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Signals from skin cells controlled by Rac proteins help turn certain precursor cells into white fat cells.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.