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

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

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.

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.

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

Foxp3+ Regulatory T Cells are important for immunity and tolerance, affect hair growth and wound healing, and their dysfunction can contribute to obesity-related diseases and other health issues.

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.

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.

Early diagnosis and personalized treatment are crucial for managing PCOS and preventing complications.

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

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

FGF5 gene mutations cause long hair in domestic cats.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

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

The study could not confirm if Victor Vinnetou was Mbuyisa Makhubu and suggested more evidence, like DNA tests, is needed.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Hair lipids do not protect against humidity.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

Nearly all elderly nursing home residents had a skin disease, with dry skin being the most common.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.