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Three characteristics of plasmacytoid dendritic cells help tell apart lupus-related hair loss from LPP.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

Mouse skin cancer progression involves a unique group of cells marked by ABCG2 and MTS24.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

The QuantAnts machines can find cancer markers and create CRISPR targets for them.

Too much keratin 16 in mice skin causes abnormal skin thickening and structure.

Trichoblastomas may mimic fetal skin development by having many Merkel cells, unlike adult skin.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

Higher PD-1 levels mean fewer CD8+ T cells in alopecia areata hair follicles.

Type XVII collagen may help prevent skin aging.

Rhodamin B stain is inconsistent for keratin in skin samples.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Nested PCR can reliably identify fungal infections when traditional methods fail.

Thorough history and examination are crucial for diagnosing genetic disorders like juvenile polyposis and hypomelanosis of Ito.

Different keratins have unique expression patterns in mouse skin cells.

CD34 marks potential stem cells in dog hair follicles.

Injecting certain cells into mice caused hair loss, which was preventable with a specific inhibitor.

Merkel cell polyomavirus can infect and persist in skin cells, evading the immune system, but certain treatments can control it.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

A unique skin cell similar to hair bulb melanocytes was identified, with better preservation using permanganate fixation.

A substance called poly(I:C) increases a protein called carbonic anhydrase II in skin cells, which might help with skin defense and healing.

Severe digestive issues in DRESS need early endoscopy for better treatment.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

A new type of nerve cell involved in itch perception was discovered.

High levels of human keratin 16 in mice cause skin lesions and abnormal skin development.

Type XVII collagen helps control skin cell growth and may have anti-aging effects.