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Epimorphin, a protein, plays a key role in the development of hair follicles in human fetuses, but it doesn't help in maintaining the stem cell population of the follicular skin layer.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

New treatments for prostate cancer and BPH show promise, including novel compounds that target hormone synthesis and response.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Cytochrome P-450 enzymes in the skin help break down various substances and could be targeted to treat skin conditions.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

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

Gene therapy shows promise for treating skin disorders and cancer, but faces technical challenges.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

Patients with certain skin symptoms and high ANA titers should be monitored for potential systemic lupus.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

New genes and pathways are important for testosterone production and male sexual development.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

The S100A4 protein is more common in psoriatic skin and could be a target for treating psoriasis.

Mobile phone radiation can cause DNA damage in human hair root cells.

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

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.