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A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

FGF-1 causes spiral ganglion neurites to branch more.

Two gene variants cause white spots in cattle.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

Vitamin D receptor FokI gene variation is not linked to alopecia areata.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

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

Blocking LFA-1 prevents hair loss in mice.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

A new engineered treatment shows promise in curing heart fibrosis.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

Keratinocyte growth factor promotes hair growth and reduces hair loss from chemotherapy.

Tcf3 and Lef1 are key in deciding skin stem cell roles.

Riboflavin 5′-phosphate (FMN) shows potential for treating androgen-related conditions but may be limited in treating prostate cancer.

Overactive Wnt5a disrupts hair follicle orientation in mice.

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

FGF signaling is crucial for starting feather development in chicken embryos.

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

The Itpr3 gene causes a specific hair pattern in mice.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Researchers found a gene mutation responsible for a rare hair loss condition.

Alk1 in specific cells is crucial for proper nerve branching and hair function.

Four new FGF5 gene variants cause long hair in dogs.

Netherton's disease causes multiple hair defects.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

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

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.