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DPP may help hair regrowth by improving blood vessel function under stress.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

Get3d protein helps maintain photosynthesis in plants and photosynthetic bacteria.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

A new genetic mutation was found causing hair and eye issues in a boy.

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

Sebaceous gland organoids could improve skin regeneration and treatment.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

IVIG therapy significantly improved symptoms in a patient with APS-2 and SPS.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

Noncoding dsRNA helps produce exosomes that aid in skin regeneration.

STAT5 is crucial for hair growth in 3D cultured human dermal papilla cells.

The research found specific genes that are more active in balding cells, which could be causing hair loss.

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

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

The enzyme Dgat1 is essential for healthy hair and skin by controlling retinoid levels.

Dexamethasone reduces inflammation and delays skin cell changes caused by TPA.

DMBT1 and galectin-3 may help suppress epithelial skin cancer.

MPZL3 protein helps control the size of oil glands and the growth of oil-producing cells in both mice and humans.

SDG helps reduce BPH effects in rats.

Drugs that block GSK-3 show promise for treating various diseases.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

A specific gene variation in goats is linked to better growth traits.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.