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Activating cannabinoid receptor 1 reduces certain keratin levels, potentially aiding psoriasis treatment.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

A KRT32 gene variant causes loose anagen hair syndrome.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

Human hair keratin genes are similar to mouse genes and are specifically expressed in hair follicles.

The HPV type 11 region activates hair-specific gene expression in mice.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

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

Keratin K80 is an ancient protein found in various tissues, important for cell structure and tissue differentiation.

Four specific keratins in hair follicles help understand hair structure and function.

Hhip-Cre effectively targets dermal papilla cells for gene manipulation in hair biology.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

The nude gene is important for skin and hair development.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

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

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

A stable, active version of a growth factor was made in bacteria, showing promise for medical use.

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

KRTAP genes evolved early in mammals, leading to diverse hair traits.

CRH in the skin acts like the body's stress response system, affecting cell behavior and immune activity.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.