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Hair follicle stem cells are key for hair and skin regeneration, can be reprogrammed, and have potential therapeutic uses, but also carry a risk of cancer.

The telogen phase of hair growth is active and important for preparing hair follicles for regeneration, not just a resting stage.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

The arrector pili muscle might play a role in hair loss and needs more research to understand its impact.

The document explains the genetic causes and characteristics of inherited hair disorders.

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

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

A new protein was made to detect specific skin cell growth receptors and worked in normal skin but not in skin cancer cells.

Wnt proteins from certain skin cells are crucial for normal hair growth and renewal.

Cannabinoid receptor-1 signaling is essential for the survival and growth of human hair follicle stem cells.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

The conclusion is that we need more effective hair loss treatments than the current ones, and these could include new drugs, gene and stem cell therapy, hormones, and scalp cooling, but they all need thorough safety testing.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Bexxar is highly effective as a first treatment for non-Hodgkin's lymphoma, with most patients alive and many in remission after eight years.

Lichen planopilaris is a rare, chronic condition causing hair loss, mainly in middle-aged women, and early treatment is important to prevent permanent baldness.

Hair follicles are complex, dynamic mini-organs that help us understand cell growth, death, migration, and differentiation, as well as tissue regeneration and tumor biology.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

The article concludes that hair loss is a common side effect of drugs treating skin cancer by blocking the hedgehog pathway, but treatment should continue, and more selective drugs might prevent this side effect.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

Enhancers and super-enhancers are key in controlling specific gene activity and can play a role in cancer development.

Canine hair follicles have stem cells similar to human hair follicles, useful for studying hair disorders.

The study showed that brown planaria can be used to cheaply test if local plants can stop cell growth.

Scientists created cell lines from balding patients and found that cells from the front of the scalp are more affected by hormones that cause hair loss than those from the back.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.