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DNA methylation is essential for skin and hair follicle development, and could be a target for treating skin diseases.

Mice lacking steroid 5α-reductase 2 show less aggression and better impulse control.

The enzyme for activating vitamin D is found in many body tissues, not just the kidneys.

Certain genetic markers may increase or decrease prostate cancer risk.

A 5-year-old boy grew too much hair after using minoxidil, but it went away after stopping the treatment.

Cell-mediated drug delivery systems improve skin disease treatment by using living cells for precise, prolonged, and less toxic therapy.

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.

DHEA boosts bone cell growth and differentiation in elderly stem cells.

DMSO-liposomes improve finasteride delivery for hair loss treatment.

Mefloquine, an antimalarial drug, is effective in killing melanoma cells resistant to other treatments by causing lethal stress in the cells.

Basal cell carcinomas have much higher levels of Vitamin D3 receptors compared to healthy skin.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

The FDA approved the first gene therapy for a blood disorder after overcoming early challenges and demonstrating patient benefits.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

The enzyme 25 Hydroxyvitamin D 1 α-Hydroxylase is essential for healthy skin and recovery after skin damage.

Mixed Connective Tissue Disease can develop from overlapping symptoms of several autoimmune diseases, making diagnosis complex.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

Vitamin D may help treat hair disorders.

Some vitamin D analogs can thicken skin and reduce pore size like a common acne treatment, with one analog also affecting skin growth factors.

A man developed male breast cancer after four years of finasteride treatment for an enlarged prostate.

Certain finger length ratios and body hair patterns may predict side effects from birth control pills in women.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Sex steroids affect the MafB gene differently in male and female hamsters.

Human amniotic membrane helps heal skin wounds faster and with less scarring.