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Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

Certain genes are linked to wool follicle structure and function, but not hair cycle regulation.

The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.

The research suggests that immune cells and a specific type of cell death called ferroptosis are involved in Frontal fibrosis alopecia.

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

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

BLMP-1 is important for regular molting and gene expression cycles in worms.

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

PDGFC gene may help select goats with desirable curly wool traits.

Intermediate filaments are crucial for cell structure and function, regulated by specific genes and proteins.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Biliverdin IXβ and IXδ help Pseudomonas aeruginosa adapt to chronic infections.

Epiprofin helps cells grow in developing teeth, hair, and limbs.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

The B2 genes are crucial for hair growth in rats.

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

NFIB and STAT5 work together to control specific genetic programs in cells.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

The fer-ts mutation in plants prevents root hair growth at high temperatures.

Researchers found a non-functional sheep keratin gene due to mutations.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

MOF controls skin development by regulating genes for mitochondria and cilia.

Different PADI isoforms help cells develop diverse functions.

Whale genes show changes that help them live in water, like less hair and better flippers.

Certain genes controlled by OVOL1 are crucial for creating new hair follicles.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.