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The cancer gene c-Myc increases harmful chemicals that damage DNA and can lead to cancer, but antioxidants can reduce this damage.

Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

A new mutation in the HR gene causes hair loss in a specific family.

Spiny mice have resilient, large mitochondria that help them regenerate tissue.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Mutant stem cells adapt their metabolism differently to outcompete normal cells in the skin.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Mitochondrial Complex I reduces inflammation and increases bone breakdown by affecting certain immune cells.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

Stopping mitochondrial respiration can prevent brain cancer spread in skin cancer patients, and plant compound β-sitosterol could help achieve this.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

A new DSG4 gene mutation causes hair defects in a young girl.

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

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

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

Mitochondrial reactive oxygen species are essential for skin and hair development.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

Mice without the vitamin D receptor are more prone to UV-induced skin tumors.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Keratin mutations cause skin diseases and could lead to new treatments.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.

Trichoblastomas in aged house musk shrews show unique features and may involve serum amyloid A in inflammation.