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A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

A stable sheep ovarian cell line was created for studying reproduction and hormones.

In situ DNA labeling in hair can help predict forensic DNA analysis success.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

Inositol improves metabolism, hormone balance, and reproductive health in women with PCOS and obesity.

A gene mutation in mice causes permanent hair loss and skin issues.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Revertant cell therapy could be a future treatment for Ichthyosis with confetti.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

No link between finger length ratios and color blindness was found.

DNA virus-induced tumors have consistent isozyme profiles, unlike other tumor types.

The RapidHIT ID system can effectively get DNA profiles from hair roots with enough cells.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

A 19-month-old Saudi girl had a rare skin condition with no other defects, and her family was unaffected.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

A girl had two rare hair conditions that helped understand their overlap.

A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

A new method creates unique chemical structures that could improve drug discovery.

The method helps estimate and track skin cell growth and movement during healing.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.