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BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

TLR3 signaling enhances the immunosuppressive properties of human periodontal ligament stem cells.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Pseudopelade of Brocq is a unique hair loss condition, but its cause and development are still not fully understood.

RNase L suppresses regeneration in mammals.

A new enzyme, BSSP, is found in high amounts in the hair follicles of nude mice.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

Blocking IL-17 might help treat the hair loss condition Lichen planopilaris.

Grasp protein helps maintain skin health after UVB exposure.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Blimp1 is crucial for hair follicle growth and skin health.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

Lichen planopilaris causes permanent hair loss and scarring due to damage to hair follicles and can be mistaken for other hair loss conditions.

The LAMTOR3 gene is involved in cashmere goat hair growth and is affected by certain treatments and other genes.

The PP2A-B55α protein is essential for brain and skin development in embryos.

Researchers found that the Leptin receptor is a consistent marker for hair follicle dermal cells, which may help future hair research.

Lipase H is important for hair follicle function and shaping hair fibers.

The research found changes in gene expression related to cell death in mouse skin that help understand hair follicle development and skin health.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Lymphotoxin-β is crucial for proper skin development in embryos.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

Turning off the Lhx2 gene in mouse embryos leads to slower wound healing and scars.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

Basonuclin helps identify and track hair follicle development and cycling in mice.

ACBP is crucial for healthy skin in mice.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.