Search

everythinglearnresearchcommunity

for

Search:↓

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

Iron deficiency may be related to hair loss, but there's not enough evidence to recommend iron screening or supplements for all hair loss patients.

Oestrogens are key for bone growth during puberty in both boys and girls.

Androgens may influence T cells, contributing to higher autoimmune liver disease risk in women.

Thai rice bran extracts, especially from Tubtim Chumphae rice, can significantly reduce the activity of hair loss genes, with x-tocopherol showing potential as an anti-hair loss product.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

Voriconazole can cause serious side effects, especially in long-term use.

ADT, especially enzalutamide, may increase the risk of heart rhythm problems and sudden death in men.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Some people experience severe, long-lasting side effects from fluoroquinolone antibiotics, leading to the recommendation of limited use and increased awareness of these risks.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

The timing of when the gene Bmal1 is active affects aging and survival, with its absence during development, not adulthood, leading to premature aging.

The review concludes that more research is needed to better improve the health outcomes for people with Polycystic Ovarian Syndrome.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Fibromodulin treatment helps reduce scarring and improves wound healing by making it more like fetal healing.

A specific group of slow-growing stem cells marked by Thy1 is crucial for skin maintenance and healing in mice.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

Finasteride reduces alcohol withdrawal effects, especially in female mice.

Hes1 protein is important for hair growth and regeneration, and could be a potential treatment for hair loss.

Spironolactone can cause side effects like high potassium levels and breast enlargement, and patients need careful monitoring.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

New treatments targeting specific genes show promise for treating keratin disorders.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

A male with aromatase deficiency improved bone health with estradiol treatment.