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Shi-Bi-Man activates hair follicle stem cells and promotes hair growth by changing lactic acid metabolism and other cellular processes.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

A woman with systemic sclerosis developed a unique scarring hair loss combining features of systemic sclerosis and frontal fibrosing alopecia.

Researchers found that certain RNA sequences play a role in yak hair growth and these sequences are somewhat similar to those in cashmere goats.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Specialized ribosomes affect aging in human skin cells.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

The document emphasizes the importance of ongoing research and ethical considerations in genome editing and cellular reprogramming.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

The document explains various skin conditions and their treatments.

The meeting showcased rare skin disease cases, highlighting the need for accurate diagnosis and treatment.

Different connective tissue disorders have unique symptoms and treatments, with varying outcomes and often require ongoing care from a specialist.

In 2002, various drugs caused serious side effects, including vitamin B12 deficiency, heart issues, blindness, hypersexuality, allergic reactions, blood clotting problems, pupil dilation, capillary leak syndrome, muscle breakdown, hepatitis, skin reactions, and lupus.

MCTD should be considered in children with recurring muscle issues, lupus-like symptoms, and edema.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

Advancements in nanoformulations for CRISPR-Cas9 genome editing can respond to specific triggers for controlled gene editing, showing promise in treating incurable diseases, but challenges like precision and system design complexity still need to be addressed.

Vitamin D is important for bones, hair, blood pressure, and breast development.

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

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

Hydrogel with M2-derived exosomes improves wound healing by slowly releasing exosomes that help reduce inflammation and promote tissue repair.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Gene therapy shows promise for healing chronic wounds but needs more research to overcome challenges.

Auto-antibody testing is a useful but not definitive tool in diagnosing interstitial lung diseases, and using a specific algorithm could make testing more cost-effective.

Vitamin D receptor is important for regulating hair growth and wound healing in mice.

Activating Notch signaling can kill basal cell carcinoma cells.

Anti-SSB antibodies are useful for diagnosing systemic lupus erythematosus and are linked to specific symptoms.

Early treatment and regular check-ups are crucial for lupus patients to prevent progression and improve outcomes.

Targeting a protein that blocks hair growth with microRNAs could lead to new hair loss treatments, but more research is needed.