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The research identified key proteins and genes that may influence wool bending in goats.

Adapted classification better assesses male pattern hair loss and its link to heart disease.

Trichoscopy is a quick and reliable way to diagnose hair loss in women.

The Brigham Eyebrow Tool for Alopecia is a simple and reliable way to measure eyebrow hair loss.

Dermoscopy shows that diffuse alopecia areata progresses through specific hair growth stages.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

The SOSTDC1 gene is crucial for determining sheep wool type.

Collagen makes skin stiff, and preservation methods greatly increase tissue stiffness.

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

The research suggests that immune cells and a specific type of cell death called ferroptosis are involved in Frontal fibrosis alopecia.

The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

Different types of inactive melanocyte stem cells exist with unique characteristics and potential to develop into other cells.

Skin problems after waxing led to a sarcoidosis diagnosis.

Newborn skin cells can change into wound-healing cells more easily than adult ones, which might explain why baby skin heals without scars. Understanding this could help treat chronic wounds and prevent scarring.

Lichen planopilaris involves disrupted fat metabolism, increased scarring, and mast cell activity.

Melanogenesis-related proteins may trigger immune responses in alopecia areata patients.

Newspaper articles on alopecia are often inaccurate and sometimes mix up different types of hair loss.

The symposium showed that stem cells are key for understanding and treating skin diseases and for developing new skin models and therapies.

Mutations in the P2RY5 gene cause hereditary woolly hair.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Mutations at Val-889 and Arg-752 disrupt key interactions in the androgen receptor, affecting its function.

Hair follicle stem cells are controlled by their surrounding environment.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

The research found two types of calcium in human hair, one that varies among individuals and another that is consistent across people.

Analyzing hair with this method can help understand and monitor scalp conditions and treatment effects.

Hair follicle shape determines hair type: curly, straight, or in-between.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Key genes can rewire networks, changing skin appendage types.

The Facial Psoriasis Log-based Area and Severity Index is a more effective way to measure improvements in facial psoriasis than the traditional method.