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Protein kinase C epsilon may increase skin cancer risk by affecting nearby cells.

Early diagnosis and biotin treatment are crucial for infants with biotinidase deficiency to prevent severe complications.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

Newly designed proteins can effectively degrade specific proteins in cells, offering a potential new therapy method.

Ethionine significantly inhibits wool growth in sheep but not hair growth in mice or rats.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

The cat's skin condition improved significantly with medication, with no relapse.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

A new mutation in mice causes crooked whiskers and messy hair.

Heparan sulfate is important for hair growth, preventing new hair formation in mature skin, and controlling oil gland development.

MG53 helps reduce skin damage caused by nitrogen mustard.

Ichthyosis serpentina may be a variant linked to bamboo hair, with a possible genetic component.

The naked mutation in mice causes hair loss and helps identify keratin genes.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Two children with lysinuric protein intolerance showed symptoms similar to lupus.

Cathelicidins could treat skin issues but face challenges like safety and resistance.

A person with a new mutation in the SCN1A gene developed brain inflammation after COVID-19.

High ODC and low K1 and K10 may indicate early skin tumors in mice.

The chitosan-peptide system helps cartilage regeneration using fat-derived cells.

The UHS promoter is specific to mouse hair follicles.

A woman with myotonic dystrophy had multiple skin tumors on her scalp, suggesting a genetic link.

New treatments targeting specific genes show promise for treating keratin disorders.

Extracted keratin from wool and hair can be used in medicine and bioengineering.

The Celsr1 gene is crucial for normal hair patterning in mice.

Recombinant keratins can form useful structures for medical applications, overcoming natural keratin limitations.

A Korean baby with nevus sebaceus syndrome was found to have a KRAS gene mutation.