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This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

Biotin mega-dose therapy led to dramatic improvement in a newborn with a rare metabolic disorder.

The 2012 criteria are better for diagnosing atypical lupus cases.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

Liposome-composite hydrogel microspheres are promising for safe, controlled drug delivery.

LH and hCG reduce certain protein levels in women's skin.

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

A gene mutation causes monilethrix in a Chinese family.

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

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Researchers successfully made new compounds for hormone level tests, but one attempt led to an unexpected product, correcting a past error.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

A woman with chronic hepatitis C had a rare skin condition linked to her illness.

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

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

The LTF gene may help predict and manage nonspecific orbital inflammation.

A man with a rare lung-focused form of hypereosinophilic syndrome improved with steroid treatment.

Acitretin effectively treats severe hypertrophic lichen planus.

Er:YAG laser therapy effectively treats Hailey-Hailey disease, leading to long-term remission and improved quality of life.

Low-level laser therapy may help uninfected cells but has different effects on coronavirus-infected cells.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.