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Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

PPAR β/δ is important for skin health and disease treatment, but more research is needed.

Giant axonal neuropathy changes the structure of keratin in human hair.

The same gene mutation can cause different symptoms in family members.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

A new gene variant causes glucocorticoid resistance in a mother and son.

LncRNAs play a crucial role in muscle regulation and could help develop treatments for Duchenne muscular dystrophy.

MEGA PROTAC improves prediction and ranking of protein complexes better than existing methods.

Stretched hair has a similar structure to natural silk, showing hair's elasticity involves reversible changes within its molecules.

Radiation-induced hair loss may be caused by hair growth stopping and inflammation in blood vessels.

mTORC2 is crucial for healthy skin barrier by regulating lipids and filaggrin.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Vitamin D receptor actions without binding are crucial for healthy skin and hair.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

Lack of vitamin D receptor increases skin tumor risk by boosting hedgehog signaling.

MC-1R is present in skin cells and may help reduce inflammation.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

Vitamin D receptor is essential for proper skin healing after injury.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

A woman with Rhupus and Rowell syndrome was treated successfully with medication adjustments.

A specific DNA region controls skin cell gene expression by working with certain proteins.

The structure of SRD5A reveals how it reduces steroids, aiding drug design for related health conditions.

Potassium channel openers help form elastic fibers in arteries and can treat elastin deficiency and hypertension.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

ADM hydrogels help heal radiation skin injuries.

A truncated protein linked to breast cancer may change cell adhesion.

CD98hc's role in skin health decreases with age.