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Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Different hair growth problems are caused by genetic issues or changes in hair growth cycles, and new treatments are being developed.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Baricitinib effectively promotes hair regrowth in both scalp and nonscalp areas for alopecia areata universalis patients.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Some people have a genetic variation that makes them less effective at breaking down drugs.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

Neuregulin3 affects cell development in the skin and mammary glands.

Environmental cues can change the fate and function of epithelial cells, with potential for cell therapy.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Cell polarity signaling controls tissue mechanics and cell fate, with complex interactions and varying pathways across species.

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

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Scientists developed a method to grow human fetal skin and digits in a lab for 3-4 weeks, which could help study skin features and understand genetic interactions in tissue formation.

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.

One type of progenitor cell can maintain normal skin in mice.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

Changing the environment around stem cells could help tissue repair, but it's hard to be precise and avoid side effects.

Stem cell niches are crucial for regulating stem cell behavior and tissue health, and their decline can impact aging and cancer.

The skin's layers protect, sense, and regulate the body's internal balance, but can be prone to cancer.

Wnt signaling controls whether hair follicle stem cells stay inactive or regenerate hair.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

The circadian clock is crucial for tissue renewal and regeneration, affecting stem cell functions and having implications for health and disease.

New methods have greatly improved our understanding of stem cell behavior and roles in the body.