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Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

The keratin 19 promoter effectively targets genes in specific epithelial cells in mice.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

HAIRCARECUBE TM (HCC) helps hair products work better by getting active ingredients deeper into the hair.

Reactive lipids from aging cells change the extracellular matrix, affecting cell function and inflammation.

A new test more accurately detects citrulline in hair follicles and pilomatrixomas.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

A truncated protein linked to breast cancer may change cell adhesion.

Ca 45 mainly enters rat skin and eye through biosynthesis and may be adsorbed in cartilage and glands.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

CAH requires a multidisciplinary approach, and while current treatments help, future therapies show promise.

CTHRC1 helps hair grow back, and plantar dermis mixture boosts it.

Higher CRBP1 levels are linked to more severe alopecia areata.

Hydrocortisone 17-butyrate 21-propionate ointment caused reversible side effects like skin issues, weight gain, and organ changes in dogs.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Women with non-classical congenital adrenal hyperplasia have higher levels of certain steroids, which can be reduced by treatment.

Apocynin may protect skin cells from aging and damage caused by UVB light.

IL-17 is more important than IFN-γ in causing severe hair loss in chronic alopecia areata.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

Steroidogenesis inhibitors change but don't stop androgen production in prostate cancer.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Using 5-butylpicolinate esters improves the sensitivity and reliability of detecting testosterone and dihydrotestosterone in saliva.