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A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Certain gene variations might increase the risk of a hair loss condition in Koreans.

A new mouse model helps study melanocyte cells using GFP expression.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

Over a third of women thought to have non-classical congenital adrenal hyperplasia didn't have it confirmed by genetic tests.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

Genetic variants affect minoxidil hair loss treatment success.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

Finasteride affects prostate development differently in male and female Mongolian gerbils.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

Genetics likely cause premature graying hair, not vitamin levels.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Total testosterone levels can help diagnose androgen-producing tumors and hyperandrogenism in women.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Female donor to male recipient sex mismatch and positive ACA-IgG are key risk factors for vitiligo and alopecia areata in chronic GvHD patients.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

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

Two siblings have a rare hair condition caused by a new genetic variant.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.