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Human sweat glands have a type of stem cell that can grow well and turn into different cell types.

The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

Human stem cells can help form hair follicles in mice.

A Laotian man with unusual skin changes and multiple growths in his gut was diagnosed with Cronkhite-Canada Syndrome and improved with nutritional and immune-based treatments.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

Removing Mediator 1 causes teeth cells to turn into hair cells.

Cronkhite-Canada Syndrome often leads to death within 6-18 months.

Monilethrix Syndrome causes fragile, beaded hair that breaks easily and needs early diagnosis for better care.

Scaffold-based strategies show promise for regenerating hair follicles and teeth but need more research for clinical use.

Neonatal hair can help determine drug exposure during pregnancy.

Taste disorders in Cronkhite-Canada syndrome are severe in the front of the tongue but improve with treatment.

Different ectodermal organs like hair and feathers regenerate differently, with specific stem cells and signals involved in their growth and response to the environment.

Platelet-rich plasma (PRP) is a simple, cost-effective treatment that promotes hair growth and reduces hair loss, with high patient satisfaction.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Stem cells in hair follicles can become various cell types, including neurons.

Mice without certain skin proteins had abnormal skin and hair development.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

AP-2α and AP-2β are crucial for healthy skin and hair.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Ectomesenchyme is a key source of skin stem cells.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

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

GDNF signaling helps in hair growth and skin healing after a wound.

New biofabrication technologies could lead to treatments for hair loss.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Careful selection of mice by genetics and age, and controlled housing conditions improve the reliability of hair regrowth in wound healing tests.

Sostdc1 controls the size and number of hair and mammary gland structures.

The document concludes that using stem cells to regenerate hair follicles could be a promising treatment for hair loss, but there are still challenges to overcome before it can be used clinically.