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MILL molecules are unique immune proteins in mice that don't need TAP to appear on cell surfaces.

A compound named ZCZ90 can increase muscle spindle firing, potentially helping treat muscle spasms and hypertension.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

pCLCA2 protein may help maintain skin structure and function.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

A unique gene mutation was found in a family with monilethrix.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Mitochondria change shape to meet energy needs during cell movement.

The LMNA mutation affects skin structure even in asymptomatic carriers.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

The model shows that filament flexibility and amino acid differences affect how fast intermediate filament proteins assemble.

Lamins are vital for cell survival, organ development, and preventing premature aging.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Neuromyotonia and morphoea can occur together in the same body areas.

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

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The engineered yeast strain BLYAS can quickly and sensitively detect androgenic chemicals.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.