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A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

PrPC is important for neural differentiation in cattle and mouse embryonic stem cells.

Two genetic variations in Moa buffalo help them adapt to heat.

Localized ROS production is essential for cell growth and movement in plants and animals.

Minoxidil improved hair growth in a child with a rare genetic disorder.

c-Myc, Max, and Bin1 help hair follicle cells mature and die.

The DWLSM provides detailed imaging of hair shafts and follicles with high accuracy.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Exosomal miR-199a-3p from dermal papilla cells helps control hair color by affecting melanocytes.

A boy's hair turned red because of genetic mutations, not lack of zinc.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Genetic marker rs12558842 strongly linked to male hair loss.

Teriflunomide is an effective and safe first-line oral treatment for relapsing multiple sclerosis.

FERONIA is crucial for plant growth, pollen tube reception, and sugar signaling.

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

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Rapamycin treatment helps with mitochondrial disease by reducing PKC levels.

Developing microRNA-based treatments is hard but has potential.

Spiny mice have resilient, large mitochondria that help them regenerate tissue.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.