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Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

Adding a specific gene to skin cells can help treat skin disorders like psoriasis.

Stem cells from whiskers can be transplanted to stimulate hair growth.

Enzymes that change arginine to citrulline are important for skin barrier and hair formation, and their malfunction can lead to skin conditions and hair disorders.

CCC1 is essential for pH balance and normal cell function in plants.

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

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Keratin patterns in hair follicles help understand hair growth and potential hair and nail disorders.

Trps1 plays a key role in hair follicle development and cycling.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

A unique gene mutation was found in a family with monilethrix.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

The document concludes that MGRN1 affects mouse fur color by interfering with a receptor's signaling, but its full role in the body is still unknown.

Tudor-SN is important for immune cells, and polyamines can promote hair growth.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

Too much parathyroid hormone-related protein in skin disrupts hair growth in mice.

Mouse hair element patterns vary, making it unreliable for tracking time.

Inhibiting HSP90 increases cell adaptability and survival under stress.

A mutation in mice causes hair loss and immune problems.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.