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The Indus River dolphin has low genetic diversity due to a past bottleneck and human impact.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

Sheep have 17 keratin genes, similar to humans, but with different expression patterns affecting wool and hair.

Isoquercitrin helps hair grow by activating certain cell processes.

Bacterial communities on scalp hair are unique to each person but consistent across different scalp sites.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

Two new gene mutations cause a rare hair disorder.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Isoflavone may help manage PCOS symptoms, but its effectiveness is uncertain.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Polarized microscopy helps identify hair irregularities in genetic disorders.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Damaged hair follicle stem cells may leave the skin to help maintain youthfulness.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Scientists can make stem cells that can turn into any cell type.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

Most women with PCOS have insulin resistance, especially those with phenotype B.

Scientists made all eight versions of a compound called cyoctol, but found it's not an anti-androgen and it fully breaks down in the skin.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

X-ray exposure affects developing hair follicles.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

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

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

The HCR gene contributes to psoriasis risk.