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Thyroid hormones help hair grow, reduce hair loss, and increase hair pigment.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Trichohyalin in hair can trigger immune attacks in alopecia areata.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Mitochondrial reactive oxygen species are essential for skin and hair development.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

Erythropoietin overexpression disrupts hair growth and fat formation in mice.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

The conclusion is that tritium-labeled testosterone metabolites can be made and are better converted into dihydrotestosterone in skin cells than in prostate tissue.

Merino wool fibers change shape with moisture, while human hair shape stays the same.

Stopping afatinib improved a rare scalp condition in a patient.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Glucocorticoids and thyroid hormones together are essential for fetal fat development.

Transamidases are present in the epidermis but their exact role is unclear.

A specific gene mutation causes woolly hair and hair loss.

TYK2 inhibitors show promise for treating cancer and autoimmune disorders.

Overexpressing Tβ4 in goats' hair follicles increases cashmere production and hair follicle growth.

A gene mutation causes monilethrix in a Chinese family.

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

FTase and GGTase-I are essential for skin keratinocyte health.

Grafted human scalp samples on mice can produce human hair, useful for studying hair genetics.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

Human hair follicles have their own thyroid hormone system.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

A new mutation in the HR gene causes hair loss in a specific family.

The enzyme for activating vitamin D is found in many body tissues, not just the kidneys.