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Blocking glucocorticoid receptors improves glucose metabolism in a PCOS mouse model.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Formyl-peptide receptor agonists could be new anti-inflammatory drugs.

Finasteride works better than Permixon in reducing dihydrotestosterone levels.

Toll-like receptors are important for wound healing, but can slow it down in diabetic wounds.

Mice skin has components that could help with hair growth and might be used for diabetes treatment.

Finasteride reduces dihydrotestosterone, increases testosterone, and may treat hirsutism in women.

Activating TRPV3 channels stops hair growth by killing hair follicle cells.

Men using hair loss drugs like finasteride may experience sexual side effects like erectile dysfunction, but it's unclear who will be affected and when. Treating depression and sexual symptoms is suggested, as these men often have higher rates of both. More research is needed to understand why these side effects occur.

TGF-alpha is present in sheep and ferret skin and may affect hair growth without directly stimulating cell proliferation.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

EGFR inhibitors often cause skin problems and other side effects, but these are usually reversible and can be managed to keep patients comfortable.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

We need to learn more about 5α-reductases and neuroactive steroids to safely make drugs targeting these enzymes.

Enzymes called 5α-reductases have many body functions and need more research to safely use inhibitors.

Using 5-alpha-reductase inhibitors, drugs for prostate issues and hair loss, may lead to eye abnormalities in men.

Blocking the CXCR3 receptor reduces T cell accumulation in the skin and prevents hair loss in mice.

The document concludes that targeting 5α-reductase, the androgen receptor, and hair growth genes, along with using compounds with anti-androgenic properties, could lead to more effective hair loss treatments.

5-alpha-reductase inhibitors may cause a low incidence of erectile dysfunction that decreases over time.

Non-thermal plasma treatment makes mouse skin thicker and increases growth factors without harming the tissue.

Spironolactone reduces the enzyme activity that converts testosterone to DHT, helping treat excessive hair growth in women.

Finasteride, a hair loss drug, may cause long-term sexual side effects due to changes in hormone receptor levels.

Using neurohormones to control keratin can lead to new skin disease treatments.

Epidermal stem cells are diverse and vary in activity, playing key roles in skin maintenance and repair.

Understanding hair growth involves complex interactions between molecules and could help treat hair disorders.

Low oxygen conditions increase the hair-growing effects of substances from fat-derived stem cells by boosting growth factor release.

Hormones significantly affect hair and oil gland function in the skin, and more research is needed on skin-related hormone disorders.

Acne is caused by genetics, diet, hormones, and bacteria, with treatments not yet curative.