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A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

WNT10B affects hair growth by altering gene activity in hair cells.

Biliverdin IXβ and IXδ help Pseudomonas aeruginosa adapt to chronic infections.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Biotin helps regulate proteins in the blood, which may explain its role in hair growth.

Pregnant women with PCOS have higher levels of Neurokinin B in the placenta, especially with female babies.

A new method helps find proteins in hair to identify fetal growth issues.

Higher STAT3 levels are found in hair loss areas, but not linked to hair loss severity.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

Collagen XVIII is crucial for maintaining tissue structure and function in the brain, kidneys, and hair.

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

Brodalumab effectively treated a man's severe hand and foot psoriasis.

LL-37 helps stem cells grow and move, aiding tissue regeneration and hair growth.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

IL-26 has antimicrobial and pro-inflammatory effects in the chronic skin condition Hidradenitis Suppurativa.

Lymphotoxin-β is crucial for proper skin development in embryos.

IL-1β inhibits human hair follicle growth.

Rab5c is crucial for blood stem cell development by regulating Notch and AKT signals.

Targeting the TNFRSF1B gene may help treat hair loss.

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

Skin cells and certain hair follicle areas produce hemoglobin, which may help protect against oxidative stress like UV damage.

RNase L hinders hair growth by altering immune signals.

Non-immune factors play a significant role in alopecia areata.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.