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Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

Papular acantholytic dyskeratosis of the vulva is a rare, benign skin condition that can be managed conservatively.

The vitamin D receptor is essential for skin stem cells to grow, move, and become different cell types needed for skin healing.

The model can effectively help diagnose meibomian gland dysfunction automatically.

Vitamin D affects Msx1 protein expression and may influence mineralized tissue health.

A PEG-400/oleic acid mixture best improves drug delivery monitoring through hair follicles.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Lack of small, fine hair on the front hairline is a key sign of frontal fibrosing alopecia.

Intralesional cidofovir may be a viable alternative treatment for SCC.

UVFD helps detect hair follicles in alopecia areata better than traditional methods.

Ivacaftor can protect against noise-induced hearing loss by reducing oxidative stress.

Oxytocin receptor changes in hair cells may help identify autism, especially in males.

Certain genes controlled by OVOL1 are crucial for creating new hair follicles.

Autologous cell-based therapies, especially SVF, effectively and safely improve atrophic acne scars.

Early detection of specific VDR mutations is crucial for effective treatment and better dental outcomes in children with hereditary vitamin D–resistant rickets.

Different forms of the Vitamin D receptor can impact metabolic and hormone issues in Polycystic Ovary Syndrome.

The immune processes causing VKH and vitiligo are similar in dogs and humans.

Androgens increase muscle mass by promoting myoblast growth through ornithine decarboxylase.

Vitamin D3 speeds up skin healing by helping skin stem cells grow and develop.

Early diagnosis and teamwork are crucial for managing ILVASC effectively.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

Vitamin D receptor gene changes don't affect alopecia areata risk.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

Vitamin D receptor actions without binding are crucial for healthy skin and hair.

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

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

Mice without the vitamin D receptor are more prone to UV-induced skin tumors.

Osaterone acetate reduces prostate size and enzyme levels in dogs with benign prostatic hyperplasia.

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