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A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

PDF2 senses specific lipids and regulates root growth and gene expression in Arabidopsis.

A new genetic mutation was found causing hair and eye issues in a boy.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

A gene mutation causes woolly hair in a Syrian patient.

Overexpression of PTHrP in chondrocytes causes short-limbed dwarfism and delayed bone formation in mice.

Diphencyprone initially increases mouse hair growth, then slows it, possibly due to changes in specific protein levels.

cDermo-1 causes dense skin, feathers, and scales in chickens.

New genes and pathways are important for testosterone production and male sexual development.

Different PADI isoforms help cells develop diverse functions.

Pygo2 is important for early growth and progression of intestinal tumors, and could be a target for treating cancers with certain mutations.

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

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

Deleting podoplanin in mice promotes hair growth by enhancing cell migration.

Higher levels of the DP2 receptor may lead to hair loss.

Increased PHGDH expression causes early melanin buildup in hair follicles.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Certain genes help dermal papillae cells in hair follicles grow and group together.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

The protein DDX6 helps keep skin cells renewing properly by controlling the production of certain other proteins and breaking down those that cause cells to mature too quickly.

New mutations in the DSG4 gene cause a rare hair condition.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

PrrH sRNA controls pyochelin production in *Pseudomonas aeruginosa*.

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.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.