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Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Dermal EZH2 controls skin cell development and hair growth in mice.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Alpha-MSH affects mitochondrial function, and MC1R mutations may increase skin aging.

TR3 is mainly found in hair follicle stem cells and may be involved in hair loss.

Continued ritlecitinib treatment can lead to hair regrowth in some patients with alopecia areata who initially don't respond.

Ritlecitinib effectively treats alopecia areata and is well-tolerated.

Accurate diagnosis of RDEB-mitis in older adults is crucial for proper management without immunosuppressants.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

Resveratrol activates the Nrf2 pathway in human skin, significantly increasing the production and distribution of the antioxidant glutathione.

Ritlecitinib effectively treats alopecia areata and is safe for long-term use in people 12 and older.

Cyanidin 3-O-arabinoside may help treat a common form of hair loss by protecting cells against aging and improving cell function.

Alopecia in these mice is caused by defective hair cycle communication due to missing vitamin D receptor function, not vitamin D levels.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Ritlecitinib effectively promotes hair regrowth in severe and very severe alopecia areata.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Two types of 5α-reductase are in dog skin, which might make dutasteride better than finasteride for treating dog hair loss.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

Ch55 may help reduce skin scarring and fibrosis.

Hairless protein can block vitamin D activation in skin cells.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

The vitamin D receptor helps regulate skin and hair health independently of its usual vitamin D ligand.

Rac1 is crucial for normal hair structure and pigmentation.

Anti-Desmocollin 3 antibodies can cause atypical pemphigus symptoms.

A new DSG4 gene mutation causes hair defects in a young girl.

The gene HDC is important for the development of hair follicles in newborn mice.

ARHGEF3 is essential for proper hair follicle development.

Overexpression of LRIG3 in skin causes hair loss.