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A substance called sodium zinc dihydrolipoylhistidinate can significantly reduce hair loss caused by chemotherapy in rats.

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

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Trichohyalin, a protein from pig tongue, was purified and found to have a filamentous structure.

Trichohyalin in hair can trigger immune attacks in alopecia areata.

The CRH/CRH-R1 system might be involved in causing lichen planus.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

A specific gene mutation causes woolly hair and hair loss.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

A new DSG4 gene mutation causes hair defects in a young girl.

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

HDAC1 is crucial for skin development and preventing tumors.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

LALPS causes non-scarring hair loss along the Blaschko line, with unique trichoscopic findings.

Deleting MED1 in skin cells causes hair loss and skin changes.

CCL5 is important for the hair growth potential of human dermal papilla cells.

Defective nuclear transport may cause gene expression changes in Progeria.

A specific gene mutation causes complete hair loss without other health issues.

Thymic LCH may be underdiagnosed, so thymic ultrasound should be considered in infants with cutaneous LCH.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

Genetic testing is crucial for diagnosing and managing non-Herlitz junctional epidermolysis bullosa.

Lamins are vital for cell survival, organ development, and preventing premature aging.

Mice genetically modified to produce more Del1 protein had faster hair regrowth.

Two mouse mutations cause similar hair loss despite different skin changes.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.