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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 point mutation in the androgen receptor gene causes complete androgen insensitivity.

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

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

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

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

The vector successfully directed specific gene expression in hair follicles.

Overexpression of SSAT in mice causes hair loss, liver damage, and sensitivity to polyamine analogues.

The Siah1 and Siah2 genes are active in mouse skin development and hair growth, especially right after birth.

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

A specific gene variation in goats is linked to better growth traits.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

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

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

A new method speeds up insulin amyloid fibril growth, useful for studying diseases.

Mice hair follicles take in the amino acid cystine.

A specific gene mutation causes a severe skin disorder in a family.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

Transglutaminase 2 may control sebocyte maturation and lipid metabolism.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Hypertrichosis (excessive hair growth) can help diagnose superficial epidermolytic ichthyosis.

A specific chemical change in the S100A3 protein leads to the formation of a four-part structure important for hair formation.

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

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.