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Mammary stem cells drive mammary gland growth by branching and cell mixing.

Different types of long-lasting stem cells are responsible for the growth and upkeep of the mammary gland.

Epithelial stem cells are crucial for tissue renewal and repair, and understanding them could improve treatments for damage and cancer.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

Different types of stem cells exist within individual skin layers, and they can adapt to damage, transplantation, or tumor growth. These cells are regulated by their environment and genetic factors. Tumor growth is driven by expanding, genetically altered cells, not long-lived mutant stem cells. There's evidence of cancer stem cells in skin tumors. Other cells, bacteria, and genetic factors help maintain balance and contribute to disease progression. A method for growing mini organs from single cells has been developed.

Hormone therapy for transgender females increases the risk of blood clots and requires careful dosing, monitoring, and lifelong management.

The Ovol2-Zeb1 circuit is crucial for skin healing and hair growth by guiding cell movement and growth.

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

Stem cells regenerate tissues and their behavior varies by environment, suggesting the hematopoietic system model may need revision.

Ovol2 is crucial for hair growth and skin healing by controlling cell movement and growth.

Neuregulin3 affects cell development in the skin and mammary glands.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

Keeping β-catenin levels high in mammary cells disrupts their development and branching.

Vitamin D is important for bones, hair, blood pressure, and breast development.

NF-κB signaling is crucial in many diseases and can be targeted for new treatments.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Children's hair grows in different types from before birth through puberty, with growth rates and characteristics varying by age, sex, and race.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Adult human skin can grow new fine hair follicles after a deep exfoliation treatment.

GLI2 increases follistatin production in human skin cells.

ILK is essential for proper hair follicle development and structure.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Latanoprost can make eyelashes longer, thicker, and darker.

Mouse hair follicle cells briefly grow during the early hair growth phase, showing that these cells are important for starting the hair cycle.

UV radiation can help sterilize wounds and promote healing but requires careful use to avoid damaging cells.

Human hair follicles can regenerate after removal, but with low success rate.