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The document concludes that hair loss and acne in women can be due to both androgen-related and unrelated causes, requiring a collaborative treatment approach.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

SOX4 is crucial for the development of melanoma.

Changes in NRF2 levels may contribute to hair loss in Egyptian men.

Long-term use of androgens can help manage Hereditary Angioedema (HAE) but may cause serious side effects, so alternative treatments with fewer side effects are being considered.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Chicken feather growth involves specific genes and shares similarities with hair development.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Researchers found genes linked to hair growth cycles in Inner Mongolia cashmere goats, which could help understand and treat hair loss.

Human Schwann cells can be quickly made from hair follicle stem cells for nerve repair.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

Oxytocin receptors are found in skin cells near touch and pain neurons.

The study suggests that higher levels of SIRT1 and SIRT2 may improve overall cell health and aging processes.

Planarian regeneration begins with a specific gene activation caused by injury, essential for healing and tissue regrowth.

The conclusion is that PCOS is caused by ovarian sensitivity to hormones and disrupted hormone control, possibly due to ovarian factors, and more research is needed.

Hormones during pregnancy and lactation keep skin stem cells inactive, preventing hair growth.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

The zinc finger protein 3 in Arabidopsis thaliana reduces plant growth and root hair development.

Polycystic ovary syndrome causes high male hormone levels, leading to symptoms like excess hair, acne, and fertility problems.

Type 2 inflammation helps wound healing by switching immune cells to repair mode.

Blocking JAK-STAT5 signaling in mice leads to hair growth.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Alopecia areata involves both innate and adaptive immunity, with specific genes linked to the disease.

Understanding wool keratin-associated proteins in sheep can help improve wool quality through selective breeding.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

FOXN1 gene variants cause low T cells and immune issues from birth.