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The antibody 005-C04 blocks prolactin receptors, causing reversible infertility, impaired lactation, and hair regrowth in female mice.

LPA3 is crucial for embryo implantation and links LPA to prostaglandin signaling.

A(1-7) treatment reduces symptoms of lupus in mice.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Tcf3 and Lef1 are key in deciding skin stem cell roles.

Folate receptor β helps suppress the immune system in macrophages and affects cancer growth and hair health.

Discoid lupus erythematosus involves immune activation and fibrosis around hair follicles, with shared pathways across humans, dogs, and mice, suggesting potential treatments for both humans and animals.

RXR and RAR proteins in skin may help with cell growth, hair growth, and gland function.

Lower GATA3 levels in mice help hair regrow by changing certain immune cells.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

The Fas/FasL pathway may play a role in alopecia areata.

The research mapped diverse cell types in mouse lacrimal glands, aiding understanding of gland biology and diseases.

L-borneol helps skin wound healing by promoting stem cell differentiation.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Deleting TNFα gene reduces skin cancer risk in certain mice.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

LEF1 is essential for the development of airway glands and is regulated by the Wnt/ß-catenin pathway.

LncRNAs play a crucial role in muscle regulation and could help develop treatments for Duchenne muscular dystrophy.

High levels of the protein Flightless I worsen ulcerative colitis symptoms in mice.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

XEDAR triggers a specific signaling pathway in cells.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

EP 2 receptor is essential for heart repair by helping macrophages work properly.

Rezpegaldesleukin shows promise for treating severe alopecia areata.