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PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

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

Chlormadinone acetate is a strong, well-tolerated hormone used in birth control and hormone therapy with benefits for menstrual pain and skin conditions.

The same gene mutation can cause different symptoms in family members.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

The PI's development is closely linked to skin and hair pigmentation in macaques.

Minoxidil can cause erythema multiforme, even if patch tests are negative.

Corneal health relies on cell migration and cooperation with the lacrimal gland, not Bmi1+ cells, and Eda gene mutations can cause dry eye disease.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

OR101 may effectively treat atopic dermatitis and similar skin conditions.

Increased 14-3-3 proteins may block hair cycle regression, causing hair loss.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

Dermal EZH2 controls skin cell development and hair growth in mice.

Upadacitinib effectively improved severe atopic dermatitis and alopecia universalis in a 29-year-old man.

Dimethyl fumarate speeds up wound healing in IL-36Ra deficient mice by reducing NET formation and oxidative stress.

Acetyl zingerone methyl ether protects and extends hair color while improving hair health.

A boy's hair turned red because of genetic mutations, not lack of zinc.

Using a combination of AMD3100 and FK506 can speed up and improve wound healing in diabetic rats.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

Maternal melatonin improves offspring hair growth by affecting specific proteins and pathways.

Wnt1a-conditioned medium from stem cells helps activate cells important for hair growth and can promote hair regrowth.

A gene mutation in mice causes skin defects and early death.

The naked mutation in mice causes hair loss and helps identify keratin genes.

Desmocollin 1 helps maintain skin structure during fetal development.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Most patients with dermatomyositis had skin rash and were treated with prednisolone and hydroxychloroquine.

Two microRNAs affect hair follicle development in sheep by targeting specific genes.

The demineralized bone matrix scaffold is better for cell attachment than the mineralized bone allograft.