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A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

POMC-derived peptides are important for skin functions like immune response and stress management.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

Some patients on anti-TNF drugs experience a type of hair loss called TAIAPA.

Genetics, nutrition, lifestyle, and hormones affect early grey hair, but more research is needed.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Certain vitamins and their derivatives can help hair grow longer by activating specific growth signals.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

TRPS1 loss in balding scalp areas contributes to hair loss in androgenic alopecia.

Higher 3α,5α-THP levels in the brain may reduce depression in pregnant rats.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

A higher testosterone/dihydrotestosterone ratio in PCOS patients may indicate worse metabolic health.

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

A specific gene mutation causes Olmsted syndrome.

Matriptase imbalance contributes to cancer development and spread.

The updated NPRT system now covers different types of hair loss in men and women.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

The study found genetic diversity in coat color dilution among Czech pointers in Slovakia.

Researchers converted human embryonic stem cells into trophoblast stem cells using specific transcription factors.

FGF13 gene changes cause excessive hair growth in a rare condition.

Colorectal cancer's ability to spread is due to changes in many genes, not just one.

Activating TSPO helps protect the retina from damage caused by high eye pressure in glaucoma.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.