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Cortisol increases a specific protein in bone cells, which may help explain its negative effects on bone.

CRF can cause hair loss, but blocking its receptors might prevent this.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

Lack of Crif1 in hair follicle stem cells slows down hair growth in mice.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

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

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

A protein called FERONIA helps control root hair growth in response to cold and low nitrogen by activating nutrient-sensing pathways in a plant called Arabidopsis.

A girl had rickets due to a gene mutation affecting vitamin D response.

AHR ligands could treat inflammatory skin diseases.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

MC-1R is present in skin cells and may help reduce inflammation.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Rhupus is a complex syndrome that is hard to diagnose due to unclear clinical criteria.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

Higher CRBP1 levels are linked to more severe alopecia areata.

Alopecia can be caused by multicentric reticulohistiocytosis.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

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

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

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Mutations in the hairless protein gene cause hair loss.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.