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Blocking mTORC1 may help prevent skin cancer by stopping the growth of certain skin stem cells.

Scarring alopecia involves increased immune cells and specific gene changes near damaged hair follicles.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

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

Panitumumab treatment can cause unusual hair growth in some colorectal cancer patients.

Recent findings advanced understanding of cancer mechanisms and potential treatments.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

Mitf plays a key role in melanoma progression and is linked to disease stage.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

A girl with citrullinemia developed pili torti, suggesting a link between the hair condition and the metabolic disorder.

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

SPRY1 deficiency in skin cells causes stem cells to move to the skin surface, leading to increased pigmentation.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

ALRN-6924 may prevent hair loss caused by chemotherapy.

Reduced AR gene methylation may cause early pubic hair growth in girls.

Baldness may lower the risk of testicular cancer.

High levels of ST14 and TMEFF1 proteins in ovarian cancer are linked to worse patient outcomes and may be a new treatment target.

Targeting the TNFRSF1B gene may help treat hair loss.

A specific gene mutation causes a severe skin disorder in a family.

The Kras mutation changes normal cell signals, leading to disrupted tissue structure and potential cancer.

Tumor cell adhesion is linked to higher risk of SLN metastasis and melanoma recurrence, and a model including these factors predicts these outcomes better than one with just clinical data.

A genetic variant linked to hair thinning in Japanese women was found.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

Skin cancer often starts from Lgr5+ progenitor cells.