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Melatonin can increase cashmere yield by altering gene expression and restarting the growth cycle early.

Keratin hydrogels from human hair show promise for tissue engineering and regenerative medicine.

Mf-rich hair degrades more than Ma-rich hair, especially with Proteinase K.

Hair and nails are skin parts that develop early and serve protective and functional roles.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

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

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

A rare biotin deficiency in an Iraqi family caused severe symptoms but was successfully treated with lifelong biotin.

Taking L-tryptophan supplements might cause a condition similar to scleroderma in some people, which can get better after stopping the supplement and starting corticosteroid therapy.

ILK is essential for skin development, pigmentation, and healing.

Mitochondrial Complex I reduces inflammation and increases bone breakdown by affecting certain immune cells.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Linoleic acid is essential for healthy skin, and while deficiency is rare in Western societies, it can cause dry, scaly skin and hair loss.

Ruxolitinib helped a woman with a genetic mutation regrow her hair and improved her health.

Lethal-milk mice produce zinc-deficient milk, causing health issues in pups unless supplemented with zinc.

Type B Insulin Resistance Syndrome is rare, linked to lupus, and hard to treat due to severe insulin resistance.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Children with partial biotinidase deficiency are healthy at birth but may develop symptoms that improve with biotin therapy.

A young woman with lupus was treated with hydroxychloroquine and prednisone.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

ILC1-like cells can independently cause alopecia areata.

Interleukin levels are higher in alopecia areata patients but don't predict disease severity or duration.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Modified pep7, named EPM peptide, effectively promotes hair growth at low concentrations and works well with minoxidil.

Dutasteride is more effective than finasteride for hair growth, and pregabalin effectively treats neuropathic pain.

Honey has many health benefits and is good for you.

IMA may indicate oxidative stress in skin and hair disorders, but more research is needed.

Monilethrix is not caused by a metabolic defect.