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Breast cancer patients taking CDK4/6 inhibitors are more likely to experience fatigue, hair loss, and mouth sores.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

A unique gene mutation was found in a family with monilethrix.

Super-enhancers control CD25 expression in specific cell types, affecting immune function.

Understanding genetics is crucial for treating heart and skin diseases.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

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

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

Using special RNA to target a mutant gene fixed hair problems in mice.

Understanding the APCDD1 gene can lead to new hair loss treatments.

Deleting TNFα gene reduces skin cancer risk in certain mice.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

FOXN1 duplication can cause excessive hair growth.

Krt15+ cells in mice can resist radiation, regenerate tissue, and start tumors, suggesting new cancer treatment targets.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

CDK inhibitors may help treat ARDS and psoriasis but need more testing for safety and effectiveness.

Some people have a genetic variation that makes them less effective at breaking down drugs.

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

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

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

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