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Elastic Net DNA methylation clocks are inaccurate for predicting age and health status; a "noise barometer" may better indicate aging and disease.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

Copper and iron cause keratin damage in hair by converting methionine to homocysteine.

Increasing m6A levels can improve skin cell growth and wound healing.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

ARHGEF3 is essential for proper hair follicle development.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Suppressing ODC activity reduces tumor growth in hair follicles.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

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

MicroRNA-302 helps improve the conversion of body cells into stem cells by blocking NR2F2.

A genetic hair protein variant is more common in Japanese people and is inherited.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

Key genes for mink fur have been identified, aiding conservation efforts.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

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

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

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

Artemis phosphorylation at Ser516 may help regulate skin and hair structures.

ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

A new mutation in mice causes crooked whiskers and messy hair.

Different Myc family proteins are located in various parts of the hair follicle and may affect stem cell behavior.

The study found nine new hair protein genes in human hair follicles.

Keratin 15 helps keep skin cells in a young, undifferentiated state.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.