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Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

PP2Acα is essential for proper hair and skin development.

The DNA convention was a valuable opportunity for learning and networking, especially after COVID-19.

Deleting vitamin D and calcium receptors in skin cells increases skin cancer risk by reducing DNA repair and stress response.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

PLAU and SerpinB2 affect cell death differently in various forms of leprosy and could be targets for new treatments.

Effective delivery of gene editors is crucial for safe and successful gene editing in healthcare and agriculture.

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

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Higher hair follicle density leads to more wool in rabbits, influenced by specific genes and lncRNAs.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Researchers found two new genetic variants linked to Alzheimer's disease.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

PNU 157706 is a more effective treatment than finasteride for conditions caused by DHT, like enlarged prostate and hair loss.

Higher caspase-1 levels found in balding scalps; reducing it may help treat hair loss.

Long non-coding RNAs play a key role in yak hair growth cycles.

Polydeoxyribonucleotides may help with healing and anti-aging, but more research is needed.

Certain genes may help Bulgarians live longer.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

Neprilysin is important for hair growth regulation.

Nod factor can trigger changes in legume root hairs with just one molecule.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

A substance called DKK-1 increases in balding areas and causes hair cells to die when exposed to DHT.

OR2AT4 helps reduce aging and cell damage in human skin cells.