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Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

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

New genetic mutations causing hair loss were found in a Chinese family.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.

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

Peptide nanoparticles can effectively deliver CRISPR-Cas9 to target KRAS mutations in cancer.

Five different TPO gene mutations were found in PCOS patients with thyroid hormone issues.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

PCAT1 helps hair growth by controlling miR-329/Wnt10b.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

Low-penetration genes might help personalize colorectal cancer prevention.

Hair shaft changes may be linked to CCCA, but their role is unclear.

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

PTEN was identified as a specific marker for the skin disease cutaneous lupus erythematosus, and it helps increase the expression of harmful type I interferons.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

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

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

Porocarcinoma generally has low rates of recurrence, spread to lymph nodes, and death.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

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