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

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

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

The hair disorder was caused by abnormal protein formation, making hair easily damaged.

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

Mutations in the KRT85 gene cause hair and nail problems.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

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

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

Controlling transposable elements is crucial for successful tissue regeneration.

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

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

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

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

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

Trichothiodystrophy causes unusual hair and developmental issues.

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

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

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

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

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

The technology can create transgenic cashmere goats with improved wool quality.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.