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Interferon, especially alfa interferon, is an effective treatment for cutaneous T-cell lymphoma with manageable side effects.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The document concludes that future heart disease research should account for sex-specific differences to improve diagnosis, treatment, and outcomes.

The skin's ability to produce hormones is linked to various skin conditions, and better understanding this process could lead to new treatments.

A woman with subacute cutaneous lupus erythematosus had widespread skin symptoms triggered by medication and sunlight, which improved with specific treatments.

Toxic shock syndrome is caused by a complex interaction of bacterial toxins and the immune system, and understanding this can help improve diagnosis and treatment.

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

Marie Antoinette syndrome causes sudden hair whitening, but its exact cause is unknown.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

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

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Mutations in certain receptors can cause diseases and offer new treatment options.

Sex neurosteroids cause different effects on hippocampal synaptic plasticity in males and females.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Interferons are effective for some skin conditions and cancers, but can have side effects and need more research for optimal use.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Women with greater androgen sensitivity respond better to finasteride for hair loss.

Over 50% of women over 50 experience hair loss, with minoxidil being the only proven effective treatment.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Thyroid hormones and androgens affect gene expression in frog reproductive organs differently between males and females.

The PP2A-B55α protein is essential for brain and skin development in embryos.

Melatonin treatment increases a specific RNA in goat cells that boosts cashmere growth.

Testosterone significantly affects sexual desire in both men and women, but its impact on women is more complex and influenced by psychological factors.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.