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Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

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

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Understanding drug interactions, side effects, and patient-specific factors is crucial for effective dermatological care.

A new mutation in the HR gene causes hair loss in a specific family.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Selenium supplements can help improve symptoms and metabolic markers in lupus patients.

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

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

Newly made nicotinamide compounds could potentially treat cancer.

Some newly made compounds are promising for treating enlarged prostate, hair loss, viruses, and prostate cancer, and might be better than current drugs.

A woman with anorexia improved significantly after being treated for scurvy with vitamin C, despite not showing typical scurvy symptoms.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Nineteenth-century British drama closely reflected the era's societal values and concerns.

New testosterone analogs show promise for male contraception with better activity and potentially fewer side effects.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Some new isatin compounds could be strong cancer-fighting drugs because they fit well in cancer-related proteins and have good drug-like properties.

Some curcumin-like compounds can effectively and safely block the enzyme linked to hair loss and other conditions related to male hormones.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Gender-specific analysis could improve treatment for childhood systemic lupus erythematosus.

A patient's gum problems worsened after using cyclosporine for a scalp condition, but improved with a lower dose.

Trichophyton bullosum has been found causing severe skin infections in donkeys in North Africa for the first time since 1933.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Acne can't be cured but can be managed with treatments like benzoyl peroxide and diet changes; it's costly and can lead to scarring and mental health issues.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Vitamin D levels in hair don't match those in blood, so hair isn't a reliable indicator of Vitamin D status.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.