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

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

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Reflectance confocal microscopy confirms that yellow dots are signs of damaged hair follicles in alopecia areata.

A new tool can analyze hair to detect changes due to hormones, genetics, and aging.

Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

Hair follicles could be used for targeted drug delivery, with liposomal systems showing promise for this method.

Stem cells compete for space using cell adhesion, and mutations can affect their competitive success, with implications for tissue health and disease.

Hair follicles could be used to deliver drugs effectively, with the right understanding and methods.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

Reflectance confocal microscopy can tell apart white dots on the scalp as either sweat gland ducts or hair follicle openings.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

Bimatoprost can cause longer, thicker, darker eyelashes and eyebrows.

Scientists are using clumps of special stem cells to improve organ repair.

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.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

The patient with total hair loss did not regrow hair despite treatment, indicating a poor outlook for this type of hair loss.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Hair is a complex organ, and understanding its detailed structure and growth phases is crucial for analyzing substances within it.

Hair analysis for drugs needs a better understanding of how drugs enter hair, considering factors like hair structure and pigmentation.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Scalp hair grows at 0.37 mm/day, forearm hair at 0.18 mm/day, and thigh hair at 0.30 mm/day, with no significant differences found in people with certain hair conditions.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

The review concludes that accurate diagnosis of different types of hair loss requires proper biopsy techniques and understanding the hair growth cycle and underlying causes.

The book reveals diverse patterns of hair growth in different species and advancements in hair and alopecia research.