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Gene differences may affect baldness treatment response in Korean men.

Orthosiphon stamineus leaf extract reduces oily skin and improves complexion better than zinc gluconate.

A patient with Myotonic dystrophy type 1 had multiple tongue hemangiomas and was sensitive to anesthesia.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

A new plant extract from Avicennia marina could potentially be used to treat common hair loss.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Lower vitamin D levels are linked to higher CRP levels in people with a type of hair loss called alopecia areata.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Most people in Turkey start getting gray hair around 33 years old, with factors like age, education, hair loss, skin type, family history, and anxiety playing a role.

Wild strawberry waste extract can be a sustainable cosmetic ingredient for treating acne and hair loss.

Male yak hair growth is influenced by DHT synthesis, which is promoted by 5α-red1 and AR during growth phases, while E2 may inhibit growth through ERα.

ILC1 cells contribute to hair loss in alopecia areata.

Androgens may influence bladder cancer progression by affecting cellular behavior.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Inhibitors of 11β-HSD1 show potential for treating type 2 diabetes but require more testing for safety and effectiveness.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

Vitamin E affects liver metabolism, enhancing stress resistance, reducing blood clotting, and altering hormone processing.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

The girl's condition improved with treatment, showing no new autoimmune diseases and hair regrowth.

ILC1-like cells can cause alopecia areata by disrupting hair follicle immunity, suggesting a new treatment approach.

Human sebaceous glands contain enzymes that affect androgen production and may influence sebum production and acne.

Compound 4 is a promising treatment for hair loss with low toxicity.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Blocking the enzyme 11β-HSD1 might help treat obesity and metabolic issues.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

People with hidradenitis suppurativa often have lower vitamin D levels, weaker hip bones, and altered bone metabolism markers.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Laminin-511 is involved in psoriasis development and can be regulated by cannabinoid receptor type 1.