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Scientists have created a new hair loss treatment using ultrasound to deliver gene-editing particles, which resulted in up to 90% hair regrowth in mice.

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.

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

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

Phosphorylation of certain parts of the PIN3 protein is crucial for its role in plant root growth and response to gravity.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Nitrendipine and nifedipine effectively block muscle contractions, while papaverine relaxes them and minoxidil needs high amounts to work.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

Natural 5α-reduced glucocorticoids might be anti-inflammatory with fewer side effects than current options.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

The enzyme 17β-HSD type 2 mainly performs oxidation in human sebaceous glands, which may help protect against acne.

Finasteride 5 mg/day effectively treats hair loss in postmenopausal women without hyper-androgenism.

Androgen hormones cause hair follicle scarring in hair loss, and finasteride helps reduce it.

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

Genetic variations affecting skin structure play a key role in severe acne.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

Eph/ephrin signaling is important for skin cell behavior and could be targeted to treat skin diseases.

Understanding how melanocyte stem cells work could lead to new treatments for hair graying and skin pigmentation disorders.

RACB in barley is crucial for cell polarity and nucleus positioning, aiding fungal infection.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

New cells are added to the hair's dermal papilla during the active growth phase.

Oral valganciclovir improved a patient's skin condition caused by immunosuppression.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

Pyrene excimer nucleic acid probes are promising for detecting biomolecules accurately with potential for biological research and drug screening.

S100A3 protein is crucial for hair shaft formation in mice.

Asian hair is generally straight and thick, with unique disorders and properties, and more research is needed to understand it fully.