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Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Key genes can rewire networks, changing skin appendage types.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Scientists can control how skin stem cells divide by using different treatments.

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Removing centrosomes from skin cells leads to thinner skin and stops hair growth, but does not greatly affect skin cell differentiation.

Exosomes from stem cells help repair irradiated salivary glands by boosting cell growth.

SOX11 and SOX4 help skin cells act like embryonic cells to heal wounds in mice.

Lithium chloride-treated stem cell exosomes boost hair growth by activating a specific pathway.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Disulfide bonds affect the melting behavior of hair's crystalline structure, but hair retains some stability even after these bonds are broken.

Researchers created an efficient method to extract DNA from marmoset hair, avoiding blood chimerism.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

Cells communicate with neighbors to coordinate their development.

Mutations in specific genes cause different types of ectodermal dysplasias.

Roots adapt to uneven environments by changing growth and gene expression.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.