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Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Acyzol could help treat conditions caused by zinc deficiency.

Hair follicle studies suggest that maintaining telomere length could help treat hair loss and graying, but it's uncertain if mouse results apply to humans.

Darker skin in 10-year-old girls may be an early sign of puberty.

Elephant tail-hair can show past stress levels, matching times when stressful events happened.

Gut health affects skin diseases, and probiotics might help.

Stem cells and their secretions could potentially treat stress-induced hair loss, but more human trials are needed.

Dexamethasone increases the activity of androgen receptors in human skin cells, which may link it to certain types of hair loss.

MicroRNAs could be key biomarkers and therapeutic targets for PCOS.

Bicalutamide may help treat female pattern hair loss.

Testosterone replacement therapy helps manage deficiency and has various methods, but requires careful monitoring to avoid side effects.

Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Human skin acts like a hormone-producing organ, making and managing various hormones important for skin and hair health.

CRH in the skin acts like the body's stress response system, affecting cell behavior and immune activity.

Alopecia areata is caused by immune system attacks on hair follicles, often triggered by viral infections.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

BMAL1 and Period1 genes can influence human hair growth.

Different treatments for Hidradenitis suppurativa range from antibiotics and hormonal therapies to surgery, depending on severity.

PCOS management includes lifestyle changes and medications, with ongoing research into repurposed drugs for better treatment options.

New genetic discoveries may lead to better treatments for alopecia areata.

Low testosterone can cause a heart rhythm problem in men, but fixing it can prevent the issue.

Understanding how DHT works is important for diagnosing and treating hormone-related disorders.

JAK inhibitors show promise in effectively treating hair loss from alopecia areata.

Five preservatives may disrupt hormone function and need more health and environmental risk assessment.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Hair graying may be caused by stem cell depletion from stress or melanocyte damage.

Testosterone's effects on COVID-19 are unclear and need more research.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.