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Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

EGFR-targeted cancer therapy can cause skin issues starting at hair follicles, leading to inflammation.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

MEK and BRAF inhibitors increase sebum production and accumulation, which could cause acne-like side effects.

A dog with a hereditary skin condition causing blisters and hair loss survived for a year.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

Two new gene mutations cause a rare hair disorder.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

Suppressing ODC activity reduces tumor growth in hair follicles.

A gene mutation causes monilethrix in a Chinese family.

HPV16 oncogenes disrupt the normal activity of hair follicle stem cells.

A KRT32 gene variant causes loose anagen hair syndrome.

HPV genes and estradiol increase a cancer-related signaling pathway, which may be targeted for cervical cancer treatment.

Bcl-2 overexpression protects against UVB damage but worsens hair loss from chemotherapy.

Gefitinib can cause hair and eyebrow darkening.

Beta-HPV and MCPyV are linked to certain skin cancers, with ongoing research and vaccine development.

Understanding EGFR's role in skin is crucial for better treatments and managing side effects.

Activating c-Myc in skin causes rapid cell growth and changes, but these effects are reversible.

A specific gene mutation causes different hair defects in Indian monilethrix families.

GABEB is a less severe skin condition caused by a gene mutation affecting collagen, leading to blisters and other symptoms.

The hairless protein is important for skin, hair, and may influence cancer development.

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

A man developed a rash similar to pityriasis rubra pilaris after starting sorafenib for cancer, possibly due to the drug's effect on skin cells.

A new method quickly detects hair changes from EGFR inhibitors using a microscope.