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Temporary activation of β-catenin can create new hair follicles, but ongoing activation is needed to keep hair follicle tumors.

Trichoscopy effectively diagnoses eyebrow loss, distinguishing between alopecia areata and frontal fibrosing alopecia.

Erlotinib can cause persistent excessive hair growth.

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

The document suggests recognizing "trichiatrists" as doctors specializing in hair and scalp health, using evidence-based treatments.

TGF-alpha is present in sheep and ferret skin and may affect hair growth without directly stimulating cell proliferation.

Congenital triangular alopecia is a hair loss condition present from birth or early childhood with no effective treatment needed.

Hair follicles can be used to easily create neurons and glial cells for potential nerve repair.

Accidental findings have led to new hair treatment discoveries, like using blood pressure and diabetes medications for hair loss and unwanted hair.

Trichoscopy helps tell apart Lichen planopilaris and Frontal fibrosing alopecia from other hair loss conditions.

Scientists created a long-lasting stem cell line from human hair that can turn into different skin and hair cell types.

The conclusion is that tritium-labeled testosterone metabolites can be made and are better converted into dihydrotestosterone in skin cells than in prostate tissue.

Further research is needed to improve hair regeneration using stem cells and nanomaterials.

The 3D skin model is better for hair growth research and testing treatments.

Hydrogel microcapsules help create cells that boost hair growth.

The gene HDC is important for the development of hair follicles in newborn mice.

Human dermal stem/progenitor cells can divide and differentiate more than hair follicle dermal papilla cells.

Reflectance confocal microscopy is a promising non-invasive tool for diagnosing alopecia areata incognita.

Men with thinner hair from genetic hair loss may be more likely to have an enlarged prostate.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

The research suggests that p63 and TGF-β1 may help determine tumor type and malignancy in hair follicle and sebaceous tumors.

Netherton's syndrome may have a familial link and doesn't always include atopy.

An 8-year-old girl had nail and hair issues that improved without specific treatment, but fungal nail infection was hard to cure.

PTCH gene mutations contribute to basal cell carcinoma development.

Trichotillomania is a chronic hair-pulling disorder, more common in females, treated with therapy and sometimes medication.

Hair growth and shedding involve specific cell changes and gene roles.

Mutations in the hHb6 gene cause the hair disorder monilethrix.