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A new gene, JMJD1C, may affect testosterone levels in men.

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

Histone demethylases can change gene expression and may be linked to diseases like cancer.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Histone modification is key in treating chronic inflammatory skin diseases.

Cancer can hijack the body's cell repair system to promote tumor growth, and targeting this process may improve cancer treatments.

Certain signals are important for reducing specific chemical markers on hair follicle stem cells during rest periods, which is necessary for healthy hair growth.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

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

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

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

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

CDH3-related disease causes worsening eye and hair issues.

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

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

JMJD3 and NF-κB activate Notch1, which is essential for skin cell movement and wound healing.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Genetic testing is crucial for diagnosing and managing non-Herlitz junctional epidermolysis bullosa.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.