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A new fluorescent material can detect dextran sulfate sodium, turning green when present, useful for forensic and environmental monitoring.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

Certain gene variations may increase the risk and severity of alopecia areata.

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The KDM1 gene helps Venus flytraps close by managing potassium ions.

Netherton syndrome causes specific skin and hair changes that help in early diagnosis.

Edar signaling is crucial for proper hair follicle development and function.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

The scaffold effectively prevents melanoma relapse and aids wound healing.

A new change in the WNT10A gene caused a condition leading to short hair growth in a Chinese family.

Dermal papilla cell vesicles can boost hair growth genes in fat stem cells.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

Fzd2 is important for skin and hair development through various signaling ways.

ADM scaffolds help skin heal by promoting a healing-type immune response.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

Promising treatments for EBS include anti-inflammatory drugs, antibiotics, creams, mTOR inhibitors, and gene editing, but more trials are needed.

Microbiome analysis, BEVs, and AI can improve PCOS diagnosis and treatment.

Early detection and a multidisciplinary approach are crucial for improving gastric cancer survival rates.

Researchers developed a method to grow hair follicle cells for transplantation using a special chip.

A new 3-D bioreactor system improves drug screening and reduces animal testing.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

A 3D skin model helps study wound healing better than traditional methods.

Removing certain hair follicle stem cells worsens skin reactions to allergens.

Different PADI isoforms help cells develop diverse functions.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

TEDAR is crucial for skin cell differentiation and barrier formation.