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The guidelines suggest lifestyle changes, diet adjustments, and personalized medication to manage dyslipidemia and reduce heart disease risk.

Half of people with Alopecia Areata may see hair regrowth within a year without treatment, but recovery is unpredictable.

Corticosteroids, especially prednisone, improve short-term muscle strength in Duchenne muscular dystrophy but have manageable side effects.

The conclusion is that using drugs to block the TOR pathway might slow aging and prevent age-related diseases.

Creating stronger blockers for skin enzymes might lead to better treatment for conditions like acne and excessive hair growth.

AGA causes hair loss by shrinking hair follicles due to DHT binding, and can be treated with finasteride and minoxidil.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

Hair loss needs more research for better treatments.

Estrogen therapy can reduce skin aging but has cancer risks.

The WNT signaling pathway is important in many diseases and targeting it could offer new treatments.

Transplant success has improved with better immunosuppressive drugs and donor matching.

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.

5α-reductase is essential for male sexual development and its inhibitors have potential in treating various conditions related to hormone action.

Hormones and metabolism play a complex role in prostate enlargement, and more research is needed to improve diagnosis and treatment.

Hormonal treatments, including birth control and antiandrogens, can effectively treat acne in women.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

All-trans retinoic acid causes hair loss by increasing TGF-β2 in hair follicle cells.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Keratin 15 is not a reliable sole marker for identifying epidermal stem cells because it's found in various cell types.

Alopecia Areata is an autoimmune condition often starting before age 20, with varied treatment success and a need for personalized treatment plans.

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

Animal models have helped understand hair loss from alopecia areata and find new treatments.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Correcting nutrient deficiencies may help with hair loss, but the benefits of supplements without a deficiency are uncertain and could be harmful.

Aromatase gene variation may increase female hair loss risk.