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Goat skin changes with the seasons due to genes affected by daylight and hormones.

Lipase H is important for hair follicle function and shaping hair fibers.

Too much β-catenin activity can mess up the development of mammary glands and make them more like hair follicles.

The conclusions are: fecal short-chain fatty acids may help prevent cancer, fiber intake can reduce obesity, weight loss is hard for obese people, low BMI cancer patients are more prone to chemotherapy side effects, intermittent fasting benefits gut health, cherry laurel has health benefits in rats, certain gene variations can increase stress in hair loss patients, fecal acids can affect blood sugar levels, cold agglutinin can affect blood test results in autoimmune patients, and people with Crohn's disease have higher levels of a certain chemical in their blood.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

Primary cilia affect the size and oil production of eye glands but not the oil's makeup.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Macrophages are more involved in Lichen planopilaris than in Frontal fibrosing alopecia.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Researchers found a way to create cells from stem cells that act like human cells important for hair growth and could be used for hair regeneration treatments.

Hair loss patients have different microbes in hair follicles, possibly affecting hair loss.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Human nails and hair follicles have similar gene activity, especially in the cells that contribute to their growth and development.

New technologies help us better understand how skin microbes affect skin diseases.

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

Fine wool sheep have more genes for wool quality, while coarse wool sheep have more for skin and muscle traits.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

Botryococcus terribilis Ethanol Extract may reduce inflammation by changing gene expression in cells.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

The study found that expanded skin regenerates similarly to normal skin, with 77 genes playing a role in the process.

Super-enhancers controlled by pioneer factors like SOX9 are crucial for stem cell adaptability and identity.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

Telogen is an active phase with important biological processes, not a resting phase.

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

ILK is essential for skin development, pigmentation, and healing.