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New methods to improve the healing abilities of mesenchymal stem cells for disease treatment are promising but need more research.

A woman developed a rare scalp condition after starting minoxidil, which was resolved with specific shampoo and solution.

The document concludes that using LC-MS/MS for measuring androgens is more accurate than older methods, but it needs careful validation and standardized references to be most effective.

The hair follicle dermal sheath is essential for hair shedding and needs to communicate with the outer root sheath for normal hair growth cycles.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

New genetic mutations linked to rare skin disorders were found in three newborns.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

Scientists made a mouse that can be made to lose hair and then grow it back.

The research identified genes that explain why some sheep have curly wool and others have straight wool.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

Polycystic ovarian shape is a genetic sign of PCOS and its hormonal and metabolic features can be inherited.

Skin health and repair depend on the signals between skin stem cells and their surrounding cells.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Different types of stem cells in the skin contribute to the variety of melanoma forms.

Sensitive scalp has higher pH, more redness, abnormal sebum, and altered bacterial makeup.

Psoriasis, acne, and hair loss are linked to unhealthy cholesterol levels, increasing heart disease risk.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Women with a certain type of hair loss have more copper in the back of their head than the front, and treatment can normalize hair but not copper levels.

Activating Nrf2 in skin cells speeds up wound healing by increasing the growth of certain stem cells.

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

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.