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The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

A new gene variant causes glucocorticoid resistance in a mother and son.

Two patients with Cronkhite-Canada syndrome achieved remission after treatment.

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.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

A substance from Caulerpa racemosa seaweed may protect against skin damage caused by air pollution by reducing oxidative stress and cell death.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Early diagnosis and nutritional support are crucial for managing Cronkhite-Canada Syndrome.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

Cadd4 effectively reduces cholesterol levels without side effects.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

Calretinin identifies the companion cell layer in human hair follicles.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

Clim proteins are essential for maintaining healthy corneas and hair follicles.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

Cimicifuga racemosa extract may help prevent and treat prostate issues by inhibiting 5α-reductase.

The conclusion is that the cornea has two types of stem cells, with Lrig1+ cells being key for renewal in aging corneas, independent of CD44.

circRNA-1926 helps goat stem cells turn into hair follicles by affecting miR-148a/b-3p and CDK19.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

5α-Reductase helps regulate hormone action in toad testes, especially during breeding season.

Neuroactive steroids affect cocaine's rewarding effects through the ς₁ receptor.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A specific genetic deletion in goats affects cashmere yield and thickness.

CCCA can appear as patchy hair loss in younger men, not just the usual pattern.