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New mutations in hair keratin genes cause the rare hair disorder monilethrix.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Vaccines and targeting TrxR variants can help prevent cancer and reduce metastasis.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

A mutation in the KRTHB5 gene causes hair and nail issues.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

A specific gene change in APCDD1 increases the risk of hair loss.

Overexpressing the Tβ4 gene in goats can increase cashmere production.

TRM21 helps control flavonoid production and root hair growth in Arabidopsis thaliana.

Controlling transposable elements is crucial for successful tissue regeneration.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

A mutation in the KRT25 gene causes woolly hair and hair loss.

Identical p53 gene mutations in different cancers suggest the need for careful treatment.

Cyclic nucleotide-gated channels are crucial for proper root hair growth and calcium balance in plants.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A gene mutation in mice causes permanent hair loss and skin issues.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.