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Vitamin D receptor is important for regulating hair growth and wound healing in mice.

Sheep and goat hair fibers are complex due to keratin-associated proteins, which are important for fiber properties and growth.

Fasting in hens affects thyroid hormones, which regulate feather and hair growth.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

Hoxc genes control hair growth through Wnt signaling.

Aromatase gene variation may increase female hair loss risk.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

The PP2A-B55α protein is essential for brain and skin development in embryos.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

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

RNA editing significantly affects hair growth and follicle cycling in the Tianzhu white yak.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Fish teeth and taste bud densities are linked and can change between types due to shared genetic and molecular factors.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Cepharanthine is a well-tolerated drug with multiple medical uses, including anti-inflammatory and anti-cancer properties.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Androgens can both increase body hair and cause scalp hair loss.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

Activating β-catenin increases melanocytes and decreases Schwann cells.

DNA changes in tetraploid wheat improve root growth and nitrogen use.

LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

Mutations in certain receptors can cause diseases and offer new treatment options.