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A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

Intralesional methotrexate and triamcinolone acetonide are more effective than Vitamin D3 for treating alopecia areata.

Thioglycolic acid and L-cysteine change hair structure differently during perms, affecting hair strength and curling efficiency.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

Gujian oral liquid reduces osteoarthritis symptoms by targeting inflammation.

Ritlecitinib effectively regrows scalp, eyebrow, and eyelash hair in Asians with alopecia areata and is safe.

m-Aminophenol in hair dye can cause skin cell toxicity and stress responses.

Akt2 and SGK3 are both important for normal hair growth and development.

Thymosin β4 helps with healing, inflammation, and organ protection.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Anti-Ku antibodies are linked to unique symptoms and may involve autophagy issues.

Keratin proteins in hair are complex and come from multiple gene families.

Ketoconazole may help regrow hair and increase follicle size, but more research needed.

Hair cystine levels may indicate protein malnutrition, but more research is needed.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

Shallot extract effectively lowers blood sugar levels.

Energy healing treatment improved L-cysteine's stability, solubility, bioavailability, and shelf-life.

Ginseng extracts protect brain cells and reduce damage in diabetic rats.

Ritlecitinib significantly improves scalp hair regrowth in alopecia areata patients over time.

Alitretinoin helped clear up a skin condition called generalized granuloma annulare in an elderly man.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Lack of TG2 increases fat storage and lowers cell cleanup in skin oil cells.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

MK-386 lowers DHT in blood and skin but not in semen.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

The model and estimator can predict drug exposure in kidney transplant patients well.

Human liver cells stick to hair protein materials mainly through the liver's asialoglycoprotein receptor.