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A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

The document concludes that regenerating functional ectodermal organs like teeth and hair is promising for future therapies.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

Researchers created early-stage hair-like structures from skin cells, showing how these cells can self-organize, but more is needed for complete hair growth.

Strong skin creams work well for long-term scalp inflammation in Rapp-Hodgkin Ectodermal Dysplasia.

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

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

The study found that the protein Dkk4 helps regulate hair growth by controlling Wnt signaling in mice.

Triparanol therapy can cause hair loss and skin dryness without inflammation or damage to hair follicles or skin structures.

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.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

Scientists made structures that look like human hair follicles using stem cells, which could help grow hair without using actual human tissue.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

Lanyu pigs show that partial-thickness wounds can partially regenerate important skin structures, which may help improve human skin healing.

The molecule Wise is involved in the development of various structures in chick embryos.

Newly divided skin cells quickly move to join skin structures due to tissue tension and specific signals.

Scientists turned mouse stem cells into skin cells that can grow into skin layers and structures.

The research reveals how early embryonic mouse skin develops from simple to complex structures, identifying various cell types and their roles in this process.

Nail stem cells and Wnt signaling are important for fingertip regeneration but not sufficient for regenerating more complex limb structures.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Fungal infection was the main cause of hair loss in Egyptian children studied.

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

The study found that sweat glands contain different types of stem cells that help with healing and maintaining healthy skin.

Scientists have found a way to create hair follicles from skin cells of newborn mice, which can grow and cycle naturally when injected into adult mouse skin.

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

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.