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Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

Recurrent NICF is a rare skin condition with unclear causes, involving follicle inflammation and crystal deposits.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

NKCC1 transporters help control neuron excitability and inhibition.

AtCSLD3 and GhCSLD3 genes enhance root growth and cell elongation in plants.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

N-WASP is essential for healthy skin and preventing inflammation.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Patients with nevus comedonicus suppurativa should be monitored for diabetes.

Wnt1a helps keep cells that can grow hair effective for potential hair loss treatments.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

MEF2C is crucial for normal hair cycle progression.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

GCN reduces lung inflammation and damage from air pollution in mice.

CARI ONE helps start hair growth and makes hair follicles bigger and more numerous.

Skin cancer often starts from Lgr5+ progenitor cells.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

β-catenin helps hair follicle stem cells grow by activating a specific cell pathway.

Two patients with Cronkhite-Canada syndrome achieved remission after treatment.

Human prostate cells produce more WISP1/CCN4 when there's not enough oxygen.

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

CD44 variant changes start alopecia areata, but don't maintain it.

Higher CRHR1 levels in AA patients lead to increased inflammation.

Certain circular RNAs may regulate wool follicle growth in sheep.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.