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The study found markers indicating that cells responsible for hair color are differentiating in specific areas of the hair follicle.

Polyamines help fix DNA damage accurately in cells.

Human hair contains many proteins, with some being highly abundant and modified.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

The N gene affects the protein makeup of mouse hair.

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

MPZL3 protein helps control the size of oil glands and the growth of oil-producing cells in both mice and humans.

Researchers found new genes involved in hair growth, which could help develop new hair treatments.

Blocking casein kinase 1 in skin cells can help melanocyte precursors move better, potentially helping with conditions like vitiligo or gray hair.

Keratins 6, 16, and 17 increase in damaged or diseased skin and may help diagnose skin issues.

miR-203a-3p helps hair follicle stem cells become specialized by targeting Smad1.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Keratin peptides in hair might help identify gender and ethnicity.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Exosomal miR-199a-3p from dermal papilla cells helps control hair color by affecting melanocytes.

The research found specific genes and pathways that control fur development and color in young American minks.

A gene mutation in Lama3 is linked to a common type of hair loss.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

Epigenetic changes are crucial for stem cell behavior in skin wound healing and their disruption may lead to cancer.

Keratin 79 cells help form and regenerate hair canals.

Ptprq has multiple forms that change during inner ear development.

Keratin structure in hair is stable at pH 5-6 but disrupts between pH 6-7.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

HOTTIP and miR-10b contribute to glioma therapy resistance by affecting cell behavior, suggesting they could be targets for treatment.

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

AL136131.3 slows hair growth by affecting energy processes in hair loss.