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E6/E7 oncogenes in hair follicles cause continuous hair growth by skipping the resting phase.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Collagen XVII is crucial for skin cell growth and nail health.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

A new gene mutation causes a rare type of hair loss.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

The protein p21 is more abundant in normal skin cells than in melanoma cells and may help protect against melanoma, with UVB light affecting its levels.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

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

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

A new gene mutation causes insulin resistance in a girl and her mother.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Hair loss gene linked to prostate issues.

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

The gene p53 is crucial for removing damaged cells to allow for healthy tissue renewal.