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Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

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

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

MG53 helps reduce skin damage caused by nitrogen mustard.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

BMP signaling affects hair color by interacting with the MC-1R pathway.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

SPARC likely aids in tissue remodeling during the hair cycle, not in starting new hair growth phases.

Matriptase imbalance contributes to cancer development and spread.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

GSDMA deficiency slows skin cancer growth.

The Gsdma3 gene is essential for normal hair development in mice.

Blocking a protein called prostaglandin D2 might help treat hair loss.

The Msi2 protein helps keep hair follicle stem cells inactive, controlling hair growth and regeneration.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

The gp130 receptor helps in tissue regeneration and disease progression, and manipulating it could improve healing and prevent disease.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

The research suggests that SFRP2 and PTGDS proteins might be indicators of female pattern hair loss and could contribute to hair loss.

Both SMS1 and SMS2 are crucial for normal hair growth and cycle in mice.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

Deleting MPZL3 increases skin oil production and reduces body fat.

Minoxidil boosts hair growth in genetically modified mice.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

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

The PML protein helps prevent skin cancer in mice.

STEAP3 protein might help treat hair loss, but more testing is needed.

A special receptor in sensory nerve endings helps control how they respond to stretching.