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Plant extracts like Avicennia marina, Boehmeria nipononivea, and Camellia sinensis could potentially treat hair loss with fewer side effects than synthetic drugs.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

The document concludes that androgenetic alopecia is common, has a genetic link, and can be diagnosed and treated with medications like finasteride and minoxidil.

New genes linked to male pattern baldness were found on chromosome 20p11.

Combining stem cell-conditioned media with anti-androgen drugs can improve hair growth in male pattern baldness.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

A baby with KID syndrome died from infections and organ failure at 18 months old.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

Asian hair loss differs from Europeans; consider individual needs and psychological well-being for treatment.

Asian hair is generally straight and thick, with unique disorders and properties, and more research is needed to understand it fully.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Male hormones cause different growth in identical human hair follicles due to their unique epigenetic characteristics.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

The document concludes that combination therapy is most effective for treating excessive hair growth in women with idiopathic hirsutism, and more research is needed to understand the condition.

Proteolytic enzymes damaged hair follicle stem cells in transgenic mice.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

Terbinafine is the most effective treatment for tinea capitis, a scalp infection often confused with other conditions.

Researchers created human cells that can turn into sebocytes, which may help study and treat skin conditions like acne.

The protein hairless is important for hair regrowth because it stops the protein wise from blocking the hair cycle.

Researchers found genes linked to hair growth cycles in Inner Mongolia cashmere goats, which could help understand and treat hair loss.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

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

The study found that expanded skin regenerates similarly to normal skin, with 77 genes playing a role in the process.

Studying rare genetic disorders can help us understand and treat common diseases better.

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

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

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.