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Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Surface-modified nanostructured lipid carriers can improve hair growth treatments.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Using radiation to make mice's hair turn gray helps study and find ways to prevent or reverse hair graying.

George Ernest Rogers was a notable scientist who made important discoveries about hair and wool proteins.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

The document emphasizes the importance of ongoing research and ethical considerations in genome editing and cellular reprogramming.

MDSC-Exo can treat autoimmune alopecia areata and promote hair regrowth in mice.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Hard skin features like scales, feathers, and hair evolved through specific protein changes in different animal groups.

SOX9 is essential for the development of various organs and hair follicles.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Exosome treatment for hair growth is promising but not FDA-approved and needs more research on safety and how it works.

The document concludes that using stem cells to regenerate hair follicles could be a promising treatment for hair loss, but there are still challenges to overcome before it can be used clinically.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

The symposium highlighted the importance of genetics in understanding and treating complex skin diseases.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Oxidative stress worsens PCOS by damaging cells and disrupting metabolism, suggesting antioxidant treatments might help.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

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.

Not getting enough minerals can lead to health problems and shorter lifespans.

Natural compounds, especially Withaferin-A, may help treat post-COVID-19 complications, but some may have side effects.

Long-haul COVID can cause lasting symptoms affecting many body systems and may be linked to ongoing inflammation and immune system issues.

Laser hair removal is safe with the right settings, but side effects like pain and skin changes are more common in darker or tanned skin.

Adult stem cells from rat whisker follicles can regenerate hair follicles and sebaceous glands.

Transplantation is effective for stable leucoderma but not for progressive, widespread vitiligo vulgaris.