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

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

ATP-sensitive potassium channels are important for hair growth.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

Deleting podoplanin in mice promotes hair growth by enhancing cell migration.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Mrp3 may aid in wound healing and hair growth.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

Pannexin 3 is important for bone formation and the development of bone cells.

p63 is essential for controlling epithelial stem cells and tissue health.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Phospholipids help plant proteins move by regulating receptor interactions.

The piRNA pathway genes are crucial in early development and may influence sex differentiation through hormone regulation.

PDCD4 protein levels, affected by genetics and breastfeeding, may predict breast cancer treatment response.

p63 controls Satb1 to help skin develop properly.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Mrp3 helps in wound healing and hair growth.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.