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Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Pyrene excimer nucleic acid probes are promising for detecting biomolecules accurately with potential for biological research and drug screening.

Chitosan and melatonin together improve wound healing and have potential in medicine and cosmetics.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Mutations at Val-889 and Arg-752 disrupt key interactions in the androgen receptor, affecting its function.

A boy's hair turned red because of genetic mutations, not lack of zinc.

New mouse models of Pemphigus show severe symptoms and need better treatments.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

A mutation in mice causes hair loss and immune problems.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

Scientists successfully created and analyzed the structure of a part of the human androgen receptor with specific modulators and a peptide to understand how it binds differently in various tissues.

New peptides can delay aging and improve cell function.

The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

3D-cultured cells in HGC-coated environments improve hair growth and skin integration.

MIM is crucial for hair follicle formation and regeneration by controlling cilia formation and hedgehog signaling through its interaction with Cortactin and Src.

The hydrogel speeds up skin wound healing effectively.

Scientists can now create skin with hair by reprogramming cells in wounds.

Specific keratin gene mutations can cause monilethrix.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The HCR gene contributes to psoriasis risk.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.