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

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Some people have a genetic variation that makes them less effective at breaking down drugs.

Hydroxychloroquine may help treat benign prostatic hyperplasia by reducing inflammation and promoting cell death.

Combining NB-UVB 311 nm therapy with standard treatment improves hair regrowth in children with alopecia areata and atopic dermatitis.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

Tiny particles from 3D-grown skin cells speed up wound healing by promoting blood vessel growth.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

Docosahexaenoic acid (DHA) may help hair growth by promoting dermal papilla cell proliferation.

A simple classification based on symptoms helps diagnose and treat inherited skin disorders in Japan.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Vitamin D may help regulate cholesterol and influence prostate cancer development.

Generalized glucocorticoid resistance causes hormone imbalances and varied symptoms due to gene mutations.

Using minoxidil for hair growth may cause skin lesions in some people, and taking breaks from nitrate patches for angina might worsen symptoms.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

CYB5R1 and IL1A genes may be linked to different types of acne scars.

The new Hairless R/J mice model improves imaging for tumor monitoring and cancer therapy evaluation.

Genetic factors, skin barrier, immune function, and obesity influence risk of fungal skin infections.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.

Vitiligo is influenced by genetics and environment, and combining these factors can improve early detection and prevention.

Ca²⁺-mediated protein citrullination controls cell growth in the CNS and may help treat brain tumors.

Yak hair follicles adapt to cold through specific gene regulation, enhancing cell growth.

ARWH is a rare hair disorder with no cure, but potential treatments include minoxidil and other therapies.

Key genes like KRT27 and IGF-2 are crucial for hair follicle development in Qianhua Mutton Merino sheep.

Combining genetic and physical data improves diagnosis and treatment for early-onset monogenic diabetes.

Variegated coat color in cats is linked to the Silver locus.