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Vav2 changes how hair follicle stem cells' genes work as they age, which might improve regeneration but also raise cancer risk.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Male hormones affect COVID-19 severity and certain drugs targeting these hormones could help reduce the risk.

Hair loss linked to higher heart disease risk in both men and women.

Products should be called 'sperm-safe' only after thorough, well-designed tests.

The protein StAR is found in 17 different organs and can affect hair loss and brain functions, but its full role is not yet fully understood.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Melatonin may help treat PCOS symptoms in rats.

A natural steroid in the body may protect against eye damage in glaucoma.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Some oral medications may help treat central serous chorioretinopathy, especially eplerenone, but more research is needed.

Low doses of BPA can increase prostate growth and change hormone levels in adult rats.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Topical L-thyroxine may help with wound healing and hair growth but should be used short-term due to potential risks.

Finasteride affects frog testes by increasing testosterone, decreasing 5α-DHT, and impacting genes related to reproduction and other functions.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Immune cells are essential for early hair and skin development and healing.

Targeted immunotherapy could be a promising new treatment for hair regrowth.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Sex hormones affect hair growth and loss, and treatments for related hair diseases include various medications, hair transplantation, and light therapy.

We now understand more about what causes acne and this could lead to better, more personalized treatments.

PPAR alpha may help in hair growth and could be a target for treatment.

Stopping mitochondrial respiration can prevent brain cancer spread in skin cancer patients, and plant compound β-sitosterol could help achieve this.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.