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Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Certain gene variations may increase the risk of PCOS in South Indian women.

Regular endoscopic checks are crucial for Cronkhite-Canada syndrome patients to catch potential cancers early.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

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Finasteride may help treat chronic CSC, improving vision.

CNGC14 is crucial for calcium entry needed for root hair growth in plants.

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A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

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

Lactobacillus paracasei HY7015 helps hair grow in mice.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Cancer prevention has advanced significantly, with some strategies proving successful.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

SCUBE3 is a potential target for cancer and alopecia treatment but is challenging to target due to its varied roles.

The 3D-SeboSkin model effectively simulates Hidradenitis suppurativa and is useful for future research.

Genetic factors in PCOS are complex, with potential influences from the MC4R gene.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

Phytosomal nanocarriers can significantly increase the bioavailability of Cuscuta reflexa extract.

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SIRT7 protein is crucial for starting hair growth in mice.

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