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TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

Alopecia areata is an autoimmune disease where T cells attack hair follicles.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Human hair proteins vary by individual, body site, and ethnicity, useful for forensics.

Notch signaling disruptions can cause various skin diseases.

English springer spaniels are more prone to severe sebaceous adenitis than standard poodles.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

Transglutaminase activity is important for skin and is found in both mammals and birds.

Polycystic ovary syndrome and iron overload share similar symptoms and can be potentially treated with blood removal, diet changes, and probiotics.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

Experts met to improve care for ichthyosis patients in Spain.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Different types of PCOS need specific diagnosis methods and treatments.

Human skin xenografting could improve our understanding of skin development, renewal, and healing.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

Different body areas in mice produce different hair types due to interactions between skin layers.

Vitamin D receptor binds similarly to natural and synthetic ligands, affecting gene regulation.

Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

Future hair cosmetics will be safer and more effective.

Lysophospholipids like LPA and S1P are important for hair growth, immune responses, and vascular development, and could be targeted for treating diseases.

Progerin affects cell shape but not hair or skin in mice.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

TGase 3 helps build hair structure by forming strong bonds between proteins.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

Phospholipase A2 enzymes play key roles in skin health and disease.