Search

everythinglearnresearchcommunity

for

Search:↓

Autophagy helps keep skin healthy and may improve treatments for skin diseases.

Iron deficiency might contribute to hair loss in women.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

A group has developed therapies that show promise for treating cancer and various other conditions.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

Acne can't be cured but can be managed with treatments like benzoyl peroxide and diet changes; it's costly and can lead to scarring and mental health issues.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Managing oxidative stress might help treat low testosterone and related chronic diseases in aging men.

The document concludes that alopecia has significant social and psychological effects, leading to a market for hair loss treatments.

Pregnancy can change skin disease severity, with some conditions improving and others worsening, and treatment should balance benefits and fetal safety.

Blocking COX, especially COX-2, in the skin can reduce inflammation and pain and may help prevent skin cancer.

Toxic shock syndrome is caused by a complex interaction of bacterial toxins and the immune system, and understanding this can help improve diagnosis and treatment.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

Mouse skin can produce and process serotonin, with variations depending on hair cycle, body location, and mouse strain.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

BcFLA1 protein is crucial for root hair growth in response to low phosphate in Brassica carinata.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Disabling the FGF5 gene in sheep leads to longer wool.

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.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

Skin healing from blisters can delay hair growth as stem cells focus on repairing skin over developing hair.

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

When skin blisters, healing the wound is more important than growing hair, and certain stem cells mainly fix the blisters without helping hair growth.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

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

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.