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No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

SSEA-4 can distinguish between eccrine and apocrine sweat gland ducts.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Slug (Snai2) helps regulate hair growth timing in mice.

RSPO1 could help create new diabetes treatments by increasing pancreatic β cells.

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

Genetic differences affect breast cancer treatment success with tamoxifen in South African patients.

This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

TEDAR is crucial for skin cell differentiation and barrier formation.

Certain genes are linked to wool follicle structure and function, but not hair cycle regulation.

Certain genes affect udder shape in Holstein cows, important for health and milk production.

Dapagliflozin helps protect heart cells under stress by improving mitochondrial function and reducing cell damage.

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

ETS2 drives cancer progression in squamous cell carcinoma and is linked to poor patient outcomes.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

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

FGFR2 signaling controls Merkel cell formation in different skin regions.

Two specific genetic markers increase the risk of hair loss in Asian populations.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Ginsenoside Rg4 from ginseng may help hair growth by activating certain cell signals.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.