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Injected human hair follicle cells can create new, small hair follicles in skin cultures.

Tcf3 helps cells move and heal wounds by controlling lipocalin 2.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

Decomposed tritiated thymidine is less accurate for DNA tracing, and hair changes can indicate malnutrition.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

Bimatoprost, a glaucoma medication, may also help treat hair loss.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

UVB radiation harms hair growth and health, causing cell death and other changes in human hair follicles.

Reduced AR gene methylation may cause early pubic hair growth in girls.

Excessive hair growth in women often has no known cause and is not linked to race or other hormonal symptoms.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

New treatments for Hepatitis C show promise but need more research to confirm their safety and effectiveness for clinical use.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Glutamine metabolism affects hair stem cell maintenance and their ability to change back to stem cells.

Small molecule drugs show promise for advancing regenerative medicine but still face development challenges.

Certain drugs that block specific enzymes can help treat prostate diseases.

New treatments for severe hair loss often fail, but some patients see hair regrowth with specific therapies, and treatment should be tailored to the individual's situation.

The drug enzalutamide may reduce the ability of the virus causing COVID-19 to enter lung cells.

Using finasteride or dutasteride may cause long-lasting erectile dysfunction.

The document concludes with guidance for doctors on diagnosing and treating hirsutism effectively and safely.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

Disrupting Stat3 in hair follicle stem cells greatly reduces skin tumor formation.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

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.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Androgens prevent hair growth by changing Wnt signals in cells.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

The document concludes that research on sulfatase inhibitors should continue due to their potential in treating various diseases, despite some clinical trial failures.

Hair loss in balding individuals is linked to changes in specific hair growth-related genes.