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Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

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

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Tacrolimus causes fewer acute rejections than cyclosporin A in kidney transplants but doesn't necessarily improve kidney function after one year; cardiovascular risks and side effects vary between the two drugs.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Dogs with dermatomyositis, especially Collies and Shetland Sheepdogs, need better treatments for their skin and muscle inflammation.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Alopecia areata, a type of hair loss, may be passed through T cells and has genetic links, while treatments vary in effectiveness. Male pattern baldness can be treated with finasteride and is influenced by androgens in hair follicles.

A gluten-free diet significantly improves skin and health issues in people with dermatitis herpetiformis, a skin condition linked to celiac disease.

Alopecia areata is linked to thyroid autoimmunity but not type 1 diabetes.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Valproic Acid could potentially be used to treat immune-related conditions due to its ability to modify immune cell functions.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Hypothyroidism may cause certain types of hair loss.

Beta-HPV and MCPyV are linked to certain skin cancers, with ongoing research and vaccine development.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Udenafil may help hair grow by activating certain stem cells.

Targeting CD200 could be a new treatment for rheumatoid arthritis.

Scientists are still unsure what triggers the immune system to attack hair follicles in Alopecia areata.

Vitiligo affects overall health and self-esteem, needing more research and awareness.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

New targeted immunotherapies are improving treatment for inflammatory skin diseases.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

C60 fullerenes can alter protein function and may help develop new disease inhibitors.