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Scientists created a new cell line from Cashmere goat hair and found that cytokeratin 13 is a unique marker for certain skin cells.

Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

Scientists created keratinocyte cell lines from human hair that can differentiate similarly to normal skin cells, offering a new way to study skin biology and diseases.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Most people have similar hair protein patterns, but a rare variant was found in two women.

A woman had a non-cancerous skin tumor on her eyelid removed successfully.

Trichoscopy can help diagnose and monitor the progression of dissecting cellulitis.

Stem cells are in deep skin layers, while differentiating cells are in shallow layers.

Keratinocytes play a key role in skin health, but more research is needed.

Basal cell epithelioma-like changes are most similar to normal basal cells.

Type I and Type II keratin chains can form heterodimers despite sequence differences.

The conclusion is that an algorithm using trichoscopy helps diagnose different types of hair loss but may need updates and a biopsy if results are unclear.

Trichoscopy helps diagnose and treat dissecting cellulitis early, preventing scarring.

Understanding intermediate filaments helps explain hair health and related diseases.

Thyrotropin-releasing hormone may help control skin and hair growth and could aid in treating related disorders.

High ODC and low K1 and K10 may indicate early skin tumors in mice.

Four new cases confirmed the unique features of follicular porokeratosis.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

K39 and K40 are the last keratins expressed in hair development, completing the hair keratin catalog.

Recombinant keratin materials may better promote skin cell differentiation than natural keratin.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Autoimmune conditions can be linked to trichoepitheliomas, with treatment focusing on cosmetic concerns.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

The four patients have a unique type of ichthyosis affecting hair follicles.

A unique type of complex cyst was found on a man's scrotum.