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PRO-C22 can help diagnose and monitor the severity of hidradenitis suppurativa.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

Monilethrix is linked to a gene cluster on chromosome 12.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

Somatic BHD mutations are rare in Japanese renal tumors.

Keratinocyte growth factor promotes hair growth and reduces hair loss from chemotherapy.

Pityriasis amiantacea is a scalp condition with thick, greasy scales and sometimes hair loss.

In 2019, dermatology and venereology improved skin cancer imaging, advanced in treating skin conditions like psoriasis, and explored the skin microbiome's role in diseases.

New pyridine compounds effectively inhibit GSK3, a diabetes treatment target.

KRT72 gene helps form hair.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

New genes linked to male pattern baldness were found on chromosome 20p11.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

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

Mutations in the KRT16 gene can cause skin and nail disorders.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

Ambras syndrome's genetic cause is unknown, as it isn't linked to androgen levels.