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Using CRISPR for gene editing in the body is promising but needs better delivery methods to be more efficient and specific.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

Post-finasteride patients show changed neuroactive steroid levels, possibly causing erectile dysfunction and depression.

Skin stem cells maintain and repair the outer layer of skin, with some types being essential for healing wounds.

Brain hormones significantly affect hair color and could potentially be used to prevent or reverse grey hair.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

miR-218-5p helps skin and hair growth by targeting SFRP2 and activating a specific signaling pathway.

Targeting glucocorticoid action might help treat type-2 diabetes, but human trials are needed.

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

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

miR-22, a type of microRNA, controls hair growth and its overproduction can cause hair loss, while its absence can speed up hair growth.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

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.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

A gene called HDAC9 might be a new factor in male-pattern baldness.

RANK is a key target in breast cancer treatment due to its role in tumor growth and bone metastasis.

Botox increased hair count in men with baldness and might work by improving scalp blood flow.

Human enzymes can detoxify harmful substances but might also increase their cancer risk.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

The document concludes that future heart disease research should account for sex-specific differences to improve diagnosis, treatment, and outcomes.

Melatonin improves cashmere goat hair growth and quality by increasing antioxidants and reducing cell death.

The S100A4 protein is more common in psoriatic skin and could be a target for treating psoriasis.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

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

Lifestyle changes are the main treatment for PCOS, which is a complex condition requiring early management to reduce its health impacts.

Microneedle arrays with nanotechnology show promise for painless drug delivery through the skin but need more research on safety and effectiveness.