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A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

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

Indian Hedgehog helps control skin cell growth and protects against aggressive skin cancer.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Lack of TG2 increases fat storage and lowers cell cleanup in skin oil cells.

A mutation in the Sgkl gene causes defective hair growth in mice.

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

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

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

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

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

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

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

Csdc2 helps hair growth in cashmere goats by regulating specific genes.

A gene mutation in mice causes skin defects and early death.

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

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

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

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

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

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

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

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

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

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

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.