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c-kit affects hair growth and color in alopecia areata and androgenetic alopecia.

Epidermal stem cells have potential for personalized regenerative medicine but need careful handling to avoid cancer.

Mutation in hairless gene may increase hair loss risk.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Feathers are useful for researching growth, regeneration, and the effects of treatments like chemotherapy on hair loss.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Scientists have developed a method to keep chicken feather follicles alive and structurally intact in a lab for up to a week.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Mutation in hairless gene may increase hair loss risk.

Stopping S100A3 activity slows down hair growth in mice.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Hair follicle stem cells in hairpoor mice are disrupted, causing hair loss.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

The document concludes that managing skin conditions during pregnancy is important and requires specialized care.

Thyroid disease can cause hair loss and treating thyroid problems might help with hair disorders.

The Hairless gene is crucial for healthy skin and hair growth.

Hard skin features like scales, feathers, and hair evolved through specific protein changes in different animal groups.

Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

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

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

A specific gene mutation causes congenital hair loss.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

The study found nine new hair protein genes in human hair follicles.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.