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The combination of the excimer lamp and liquor carbonis detergens is more effective for scalp psoriasis than the lamp alone.

A new portable microscope can effectively monitor skin wound healing in real-time.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

PCOS is likely inherited in families, increasing risk for first-degree relatives.

DPP4-positive fibroblasts play a major role in producing proteins that lead to skin fibrosis.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Exposure to certain chemicals before birth and during childhood may affect puberty timing.

Plumbago zeylanica L. leaves may help dissolve blood clots and have antioxidant benefits.

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

Reducing reactive oxygen species can help treat nerve damage from platinum cancer drugs.

A vaccine may prevent benign prostatic hyperplasia (BPH).

The B2 genes are crucial for hair growth in rats.

Defective nuclear transport may cause gene expression changes in Progeria.

Cancer-associated fibroblasts promote tumor growth in skin cancer.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The combined treatment is more effective and safer for improving sunken acne scars.

Clascoterone is safe for the heart, even at high doses.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Lateral plate mesoderm helps create skin and amnion-like tissues for studying development and therapies.

Lichen planopilaris causes permanent hair loss and scarring due to damage to hair follicles and can be mistaken for other hair loss conditions.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

Combining PDLLA and PRP effectively reduces wrinkles and improves skin quality.

Certain metabolites are lower in women with PCOS and could be potential markers for the condition.

PROTACs offer new ways to treat hard-to-target diseases, with promising drugs for cancer in advanced trials.

PCOS is a hereditary disorder that can lead to diabetes and heart disease if not treated early.

Increased LC3 gene expression may be linked to premature graying of hair.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Early and accurate diagnosis of primary vitreoretinal lymphoma is crucial to prevent serious complications.

A specific gene mutation causes a severe skin disorder in a family.

The study aims to find the best PRP dose for treating moderate carpal tunnel syndrome.