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Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

A protein called lfTSLP is important in causing allergic and other skin diseases and could be a target for treatment.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

KRT72 gene helps form hair.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

Ets2 gene is crucial for placental development in mice.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

PDCD4 protein levels, affected by genetics and breastfeeding, may predict breast cancer treatment response.

Pemigatinib may be effective for treating ZMYM2::FGFR1 fusion-positive leukemia.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Increasing PDCD4 protein may help prevent or treat some skin cancers.

The research found specific genes that are more active in balding cells, which could be causing hair loss.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

A rabbit gene important for hair development was identified and detailed.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

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

LL-37 helps stem cells grow and move, aiding tissue regeneration and hair growth.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Exosomal miR-199a-3p from dermal papilla cells helps control hair color by affecting melanocytes.

Proper tissue repair in adult skin requires specific histone hypomethylation.

A gene mutation in mice causes skin defects and early death.

Neutrophils quickly respond to skin injury.

GhPLDα1 helps thicken cotton fiber walls by boosting cellulose production.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.