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EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

Enhanced stem cells from the placenta can help treat Graves' eye disease by stopping fat cell growth.

Idiopathic hirsutism may be linked to increased enzyme activity.

Mice with human fetal thymic tissue and stem cells developed symptoms similar to chronic graft-versus-host disease.

Human hair follicles have their own thyroid hormone system.

The GH-IGF-I axis is likely involved in the hormonal imbalances seen in non-obese women with functional hyperandrogenism.

Growth hormone therapy can improve symptoms and growth in children with Vitamin-D Dependent Rickets Type-2.

L-rhamnose may promote hair growth by boosting energy production in cells.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

A defective protein in progeria causes cell death and atherosclerosis, but a treatment targeting cell stress may reduce these effects.

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

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

Prolactin may influence skin glands and could be a target for treating acne and skin aging.

Hedgehog signaling can create new hair follicles but may also cause tumors.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

HPDAlR nanoparticles greatly improve skin wound healing without toxicity.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Graham-Little Piccardi Lassueur Syndrome is a rare skin condition with specific hair loss and skin symptoms.

The new assay can help develop products for hair re-growth.

Two specific genes are more active during hair growth in mice.

A substance called compound-1 could help increase hair growth by maintaining prostaglandin levels in hair follicles.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

Researchers created a new mouse model for studying scleroderma.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

MPZL3 protein is important for controlling hair growth cycles.