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Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Changes in NRF2 levels may contribute to hair loss in Egyptian men.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

Some drugs can cause rare but potentially deadly skin reactions, and early treatment and avoiding the drug again are key.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Diffuse alopecia in women may be related to androgens and iron deficiency, and basic hormone and nutrient screening is useful.

People with PCOS, especially if obese, often have NAFLD, linked to obesity, insulin resistance, and high androgen levels.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

The document concludes that alopecia areata is an autoimmune disease without a definitive cure, but treatments like corticosteroids are commonly used.

Keratin 17 is linked to various diseases, including cancer and skin conditions, and may be a target for diagnosis and treatment.

Hormones during pregnancy and lactation keep skin stem cells inactive, preventing hair growth.

Balding people may have higher heart disease risk.

Mesenchymal stromal cells may help treat severe COVID-19, but more research is needed to confirm their effectiveness.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Indian women with PCOS from Delhi and Srinagar show different symptoms, with Delhi women having higher obesity and blood sugar issues, and Srinagar women showing more hair growth and testosterone levels.

Polycystic Ovary Syndrome (PCOS) in teenagers is a complex condition linked to genetics and environment, often associated with obesity and insulin resistance, and is treated with lifestyle changes and medication.

Wnt proteins from certain skin cells are crucial for normal hair growth and renewal.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

Blocking cell death in certain stem cells can improve wound healing and tissue regeneration.

Mercury allergy linked to specific genes may contribute to burning mouth syndrome, and silicon might play a role in maintaining healthy hair.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

The conclusion is that managing hair loss conditions like FFA and melanoma requires individualized approaches, considering new findings and balancing treatment benefits with potential risks.

People with early onset hair loss (Androgenetic Alopecia) in Ile-Ife, Nigeria, have significantly lower iron levels compared to those with adult-onset hair loss.

Certain diets can affect skin conditions, but more research is needed to understand these relationships fully.

Haplogroup X found in Altaian population supports Amerindian origin.

Cells from certain embryo parts can induce head formation in another embryo, involving complex signaling pathways.

The document concludes that various findings in rheumatology offer insights into disease severity, treatment responses, and potential risks in medication, with some limitations due to unspecified participant numbers.