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Certain microRNAs are more common in balding areas and might be involved in male pattern baldness.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

Genetic marker rs12558842 strongly linked to male hair loss.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

Three specific proteins can turn adult skin cells into hair-growing cells, suggesting a new hair loss treatment.

Certain microRNAs are linked to various skin diseases and could be used to diagnose and treat these conditions.

Mice that can regenerate tissue have cells that pause in the cell cycle, which is important for healing, similar to axolotls.

In situ DNA labeling in hair can help predict forensic DNA analysis success.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

A special microbe helps plants absorb rock phosphate by growing on their root hairs.

Two gene areas linked to male pattern baldness found, more research needed.

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

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

Researchers found that certain RNA molecules might play a role in the growth of Cashmere goat hair.

The document concludes that understanding hair follicles requires more research using computational methods and an integrative approach, considering the current limitations in hair treatment products.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

VEGF stimulates hair cell growth and increases growth receptor levels through a specific signaling pathway.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Tissue stiffness affects hair follicle regeneration, and Twist1 is a key regulator.

A specific protein in chicken embryos links early skin layers to feather development.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.

The androgen receptor is a promising target for breast cancer treatment, especially in triple-negative cases, but more research is needed for personalized therapies.