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Too much androgen can cause hair loss; finasteride may help.

Oral retinoids are effective for various skin conditions but have side effects and should not be used during pregnancy.

There are many treatments for permanent hair loss disorders, but their effectiveness varies and there's no clear best option.

Aromatase gene variation may increase female hair loss risk.

Alopecia common in teens, may indicate endocrine issue, minoxidil effective treatment.

Men are more likely to get infectious skin diseases, while women are more prone to autoimmune and pigment-related skin conditions, influenced by biological and environmental factors.

Systemic diseases can cause hair loss, which is often reversible with treatment.

Androgens, like DHT, affect hair growth and treatments like finasteride may help.

Glycerol is essential for skin hydration in mice without sebaceous glands.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

The conclusion is that Treg-targeted therapies have potential, but more knowledge of Treg biology is needed for effective treatments, including for cancer.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

FGF signaling is a promising target for developing treatments for wounds, metabolic diseases, and cancer.

Changes to the Foxp3 protein affect how well regulatory T cells can control the immune system, which could help treat immune diseases and cancer.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Men with a family history of hair loss are more likely to experience it themselves, especially if both parents have hair loss.

Special immune cells called Regulatory T cells help control skin inflammation and repair in various skin diseases.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

Looking at skin can help find and treat serious diseases early.

Some diseases can improve the outcomes of other diseases, leading to new treatment possibilities.