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

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

A new mouse mutation causes skin and hair defects due to a gene change.

lncRNA MRPS28 regulates hair follicle development in cashmere goats, affecting cashmere quality.

CAP1/Prss8 does not activate PAR2 or inhibit PN-1.

Noncoding RNAs help determine cashmere quality in goats.

OsPHR2 gene in rice enhances root growth and phosphorus accumulation.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

Different PADI isoforms help cells develop diverse functions.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

SLC45A2 and GPNMB genes help control chicken feather color by promoting melanin.

Constant-release melatonin reduces SOX21 gene expression in goats during the hair follicle resting phase.

Certain genes in European Merino sheep help them adapt to different climates.

Woodhouse-Sakati syndrome shows varied symptoms and genetic differences within families.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Phospholipase A2 enzymes play key roles in skin health and disease.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.