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TCDD reduces EGF receptor activity and causes various developmental changes in animals.

Inhibiting PLA2 enzymes may help treat inflammatory skin diseases like psoriasis and dermatitis.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

DPP4 is important for scarring and skin regeneration, and managing its activity could improve skin healing treatments.

A peptide known for reducing wrinkles also effectively inhibits an enzyme linked to skin inflammation and acne.

ADSC-derived extracellular vesicles show promise for skin and hair regeneration and wound healing.

Cyclosporin A promotes hair growth in mice and increases a protein linked to hair growth, but it may not work the same way in humans.

WNT10A is important for tissue development and linked to various human disorders.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

iPSC-derived artificial platelets show promise for consistent and effective regenerative therapies.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

A brain-made hormone can protect against memory-related brain damage caused by harmful proteins.

Dexamethasone affects hair growth by altering levels of proteins that either promote or inhibit hair follicle growth.

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

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Methylprednisolone helps skin cells stick together better in pemphigus vulgaris.

Hex gene plays a crucial role in starting feather development in chick embryos.

Botulinum toxin type A and platelet-rich plasma together boost hair growth by activating specific growth pathways.

Prostaglandin D2 blocks new hair growth after skin injury through the Gpr44 receptor.

KID syndrome should be reclassified as an ectodermal dysplasia.

A new carrier improves skin delivery of tofacitinib for treating inflammatory skin diseases.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

Normal skin results from interactions between EGF and the Tabby mutation.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

The new patch made of cell matrix and a polymer improves wound healing and supports blood vessel growth.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

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

Prostaglandin D2 increases testosterone production in skin cells through a process involving reactive oxygen species, and antioxidants may help treat hair loss.