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An integrated treatment approach effectively managed plaque psoriasis, leading to complete symptom resolution and hair regrowth.

An integrated treatment approach effectively managed plaque psoriasis, leading to complete symptom resolution and hair regrowth.

Kikuchi–Fujimoto disease can cause scarring alopecia and should be considered in diagnosis.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

A woman with EMS showed unusual skin mucinosis without the typical hard skin syndrome, suggesting EMS can cause skin mucinosis.

Stem cells control their future role by changing ERK signal timing, affecting tissue regeneration and cancer.

Dermoscopy is useful for diagnosing facial actinic keratosis by identifying specific skin patterns.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Kenikir leaf extract nanosuspension may help inhibit breast cancer cell growth.

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People were generally happy with the home light therapy devices for hair loss.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Scientists can control how skin stem cells divide by using different treatments.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

AgK114 protein helps in hamster skin injury recovery.

The KAP 7 gene affects wool traits in Rambouillet sheep, with the BB genotype showing the best wool characteristics.

Krt15+ cells in mice can resist radiation, regenerate tissue, and start tumors, suggesting new cancer treatment targets.

Decreasing MIG6 can increase the movement and invasiveness of MEK-inhibited mutant NRAS melanoma, particularly when stimulated by EGF.

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Skin changes in Pseudoxanthoma elasticum patients can indicate the severity of related health issues.

Steroid injections improved symptoms and hair regrowth in a woman with a reaction to permanent makeup.

The Arabic Skindex-16 is a reliable and valid way to measure the impact of skin conditions on quality of life in Saudi patients.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

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The DWLSM provides detailed imaging of hair shafts and follicles with high accuracy.

Sgk3 is essential for normal hair follicle growth and maintenance.