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Progesterone and its metabolites affect myelin protein expression differently in male and female rat Schwann cells.

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

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

Deleting MPZL3 increases skin oil production and reduces body fat.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

Tissue environment greatly affects the unique epigenetic makeup of regulatory T cells, which could impact autoimmune disease treatment.

A specific gene mutation causes woolly hair and hair loss.

K15 gene is mainly active in the basal layers of hair follicles and epithelia, aiding early skin cell development.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

The KRTAP36-2 gene in sheep affects wool yield.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Protein ubiquitylation is crucial for controlling stem cell functions and could be targeted for cancer treatment.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Whn is essential for hair growth, and its malfunction causes hair loss.

Keratin peptides in hair may help identify gender and ethnicity, but more research is needed.

A new mouse mutation causes skin and hair issues, influenced by another gene.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

Keratin genes change gradually during skin cell development and should be used carefully as biomarkers.

The treatments stopped hair regrowth in mice.

RNA modifications help heal wounds and could lead to new treatments.

Meis2 is essential for touch sensation and nerve function in mice.

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

A specific RNA molecule blocks hair growth by affecting a protein related to hair loss conditions.

ILC1-like cells can cause alopecia areata by themselves.