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A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Alopecia in these mice is caused by defective hair cycle communication due to missing vitamin D receptor function, not vitamin D levels.

Cimicifuga racemosa extract may help prevent and treat prostate issues by inhibiting 5α-reductase.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Cyclosporin A, a drug, reduces TGF-β2 expression in skin cells, potentially causing excessive hair growth through a process involving the calcineurin/NFAT pathway.

The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

21-hydroxylase deficiency causes hormone imbalances leading to various symptoms, and diagnosis involves clinical and genetic tests.

Vitamin D receptor is crucial for bone health and mineral metabolism.

Men with male pattern baldness have lower levels of the antioxidant PON1.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

Targeting glucocorticoid action might help treat type-2 diabetes, but human trials are needed.

Erdr1 could be a new marker for diagnosing hair loss.

Hair loss can be a key sign of a rare type of rickets when vitamin D treatment doesn't work and advanced tests aren't available.

Ruxolitinib can help regrow hair in severe alopecia areata.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Sulfotransferase SULT1A1 activity may predict minoxidil treatment success for hair loss.

The compounds tested could potentially treat hair loss and alopecia.

Ritlecitinib effectively improves hair regrowth and physician satisfaction in severe alopecia areata over time.

Researchers developed a new method to find substances in herbs that can block a specific enzyme linked to hair loss.

Combining low-dose dutasteride with finasteride improved a man's hair loss.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Human keratinocytes do not naturally respond to androgens.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.