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A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

Mice with a specific BRCA1 mutation have a higher risk of tumors, especially in the uterus and ovaries.

The STRIPAK complex is crucial for skin cell organization and creating a functional skin barrier.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

Nested PCR can reliably identify fungal infections when traditional methods fail.

Short-term treatment with ROCKi increases skin cell growth without changing stem cell features.

Radiation-induced hair loss may be caused by hair growth stopping and inflammation in blood vessels.

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

PBX1 reduces aging and cell death in stem cells by boosting SIRT1 and lowering PARP1.

Activating Kras in mouse skin causes excess skin and hair loss.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

Dimethylarsinic acid speeds up skin tumor growth in certain mice.

CaM7 and CNGC14 interaction controls root hair growth in Arabidopsis.

A new protein was made to detect specific skin cell growth receptors and worked in normal skin but not in skin cancer cells.

Blocking certain immune signals can reduce skin damage from radiation therapy.

Human-hair keratin artificial tendons are biocompatible and degrade well in rabbits.

Stress in hair follicle cells increases certain immune-related proteins, which might contribute to hair loss conditions.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Ruxolitinib helped a woman with a genetic mutation regrow her hair and improved her health.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.