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Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

14,15-EET may help reduce poststroke pain by affecting certain brain proteins.

Inhibiting PDE8A may help treat hair loss by boosting fat cell growth and hair regeneration.

The skin produces and responds to thyroid-stimulating hormone, which is controlled by other thyroid-related hormones.

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

The equine epididymis mainly uses type 1 5α-reductase, and both finasteride and dutasteride can inhibit its activity.

Trps1 plays a key role in hair follicle development and cycling.

Human placenta extract reduces inflammation and symptoms in atopic dermatitis.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

Eyelid cells share signaling components but differ in pathway activity.

Delta-opioid receptors affect skin cell circadian rhythms, possibly impacting wound healing and cancer.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Sex steroid receptors are found in specific skin cells, affecting skin and hair functions.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Vitamin D and its receptor help regulate skin functions like cell growth, immunity, and hair cycle.

The ZIP13 variant is linked to abnormal hair quality.

Blocking neurosteroid production can lead to more seizures and faster epilepsy onset in rats.

17β-estradiol boosts APE1/Ref-1 secretion in cells and mice via a calcium-dependent pathway.

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