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

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

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

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

People with Alopecia areata have higher levels of prostaglandin D2 in their blood and tissues.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

PGD2 increases androgen receptor activity in hair cells, which could be targeted to treat hair loss.

Scaffoldin helps form hard skin structures in chicken embryos.

Scalp hair follicle cells help protect and heal skin in certain skin conditions.

The condition is likely inherited in an autosomal-dominant pattern.

Desmosomes are crucial for skin and heart development, and JNK may help regulate them.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

EPDS and MS might share an immune-related cause.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

Two distinct caspases in human skin help with cell death and skin formation.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Higher levels of the DP2 receptor may lead to hair loss.

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