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Ishige sinicola extract may help prevent muscle atrophy through its antioxidant and anti-inflammatory effects.

SII is a useful and affordable tool to assess and monitor alopecia areata.

GLI2 activates GLI1, promoting skin tumor growth and hair development.

Sphaeranthus indicus and silver nanoparticles can help treat liver cancer by killing cancer cells.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

A new syndrome may link skin, growth, mental, and hair issues.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

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

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

A new gene mutation causes insulin resistance in a girl and her mother.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

S100A4 and NMIIA promote tumor growth in glioblastoma by enhancing blood vessel functions.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Two siblings have a rare hair condition caused by a new genetic variant.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

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

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.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

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

Mutations in Far2 mice cause hair loss due to sebaceous gland issues.

Researchers found a non-functional sheep keratin gene due to mutations.