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Sex-determining genes may affect male baldness.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Active oxygen species might be involved in skin tumor growth, but their exact role is unclear.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Scientists found genes linked to hair length in Brangus cattle that could help breed heat-tolerant cattle.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Eclipta alba extract may work as an anticancer agent and help reverse drug resistance.

Stem cell therapies show promise for treating various diseases but face challenges in clinical use and require better monitoring techniques.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Selective breeding caused the unique curly hair in Mangalitza pigs.

The document concludes that stem cell inactivity is actively controlled and important for tissue repair and balance.

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

The first pediatric case of naevus trichilemmocysticus was documented.

Porphyra-334 may help reduce wrinkles and promote hair growth.

The RORα gene is active in different parts of cashmere goat hair follicles and may be influenced by melatonin, especially in December when hair growth changes.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

Two mouse mutations cause similar hair loss despite different skin changes.

Finasteride, often used for hair loss, can potentially cause cataracts.

Testosterone is crucial for development, growth, and various body functions in mammals.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

Keratin genes change gradually during skin cell development and should be used carefully as biomarkers.

Male tissue has more cell death than female tissue after ischemia, and some neurosteroids only protect female cells.

Indian Gooseberry has potential for cancer prevention and treatment and promotes hair growth.