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A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

A protein called ectodysplasin-A2 increases a hair growth inhibitor in balding cells, which could be a target for hair loss treatment.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Lipin-1 is important for skin cell differentiation and skin barrier function.

Dapagliflozin helps protect heart cells under stress by improving mitochondrial function and reducing cell damage.

PAD enzymes play a key role in hair growth and structure.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

MIM is crucial for hair follicle formation and regeneration by controlling cilia formation and hedgehog signaling through its interaction with Cortactin and Src.

Panniculitis in dermatomyositis is rare, more common in women, and may persist despite treatment.

BMP2 helps hair follicle stem cells become specialized by increasing PTEN, which causes autophagy.

The man was diagnosed with stage III multiple myeloma and treated to improve kidney function.

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

Basement membrane supports fibroblast aggregation, aiding hair follicle development.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

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

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

Human dermal stem/progenitor cells can divide and differentiate more than hair follicle dermal papilla cells.

Removing the p75 gene in mouse skin cells didn't affect their skin or hair growth.

Dihydrotestosterone changes some hormone-related gene expressions in rat pituitary glands but doesn't affect the estrous cycle.

Reducing SFRP1 can promote hair growth and may help treat hair loss.

DVI provides detailed 3D imaging of hair and shows how various products protect and enhance hair.