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A new genetic tool improves the study of hair growth and potential hair disorder treatments.

ATP-sensitive potassium channels are important for hair growth.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Some people have a genetic variation that makes them less effective at breaking down drugs.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

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

CK 15, follistatin, and Bmi-1 can help differentiate basal cell carcinoma from squamous cell carcinoma.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Hair follicle cells resist turning into skin cells.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

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

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.