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Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

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

Activated ras can protect kidney cells from a certain substance that causes cell death.

A new DSG4 gene mutation causes hair defects in a young girl.

Targeting NCoR1 can help treat heart enlargement and dysfunction.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

MOF controls skin development by regulating genes for mitochondria and cilia.

The treatments stopped hair regrowth in mice.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

MC1R gene variations affect skin, hair color, UV sensitivity, and melanoma risk.

Non-drug methods effectively managed agitation in a patient with a heart device, leading to improved mental function.

The DWLSM provides detailed imaging of hair shafts and follicles with high accuracy.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Overexpression of a specific receptor in mice skin causes skin thinning, early skin barrier formation, eye issues, and hair loss.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

High-dose intravenous iron therapy doesn't interfere with treatment improvements in IBD patients with iron deficiency anemia.

Sentinel lymph node biopsy is recommended for all types of desmoplastic melanoma due to higher rates of nodal metastasis.

Sentinel lymph node biopsy is recommended for all types of desmoplastic melanoma due to higher rates of nodal metastasis.

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

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

The new micelle formulation delivers acne treatment more effectively and safely than current gels.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.