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Stem cell behavior varies with stimuli, and lineage changes can happen without affecting stem cell division.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

Aging in one type of stem cell can cause aging-like changes in various organs.

Different conditions affect how hair proteins assemble, and certain mutations can change their structure.

Ptprq has multiple forms that change during inner ear development.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

Mouse skin cancer progression involves a unique group of cells marked by ABCG2 and MTS24.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

Krox20 is crucial for hair growth and maintaining skin stem cells.

Researchers found a gene mutation responsible for a rare hair loss condition.

Using special RNA to target a mutant gene fixed hair problems in mice.

Lack of TrkC receptor delays hair follicle development.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Mouse skin has special cells in the epidermis that decrease with age and are linked to keratinocyte stem cells.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

IL-17 and certain immune cells are linked to more severe alopecia areata.

Removing UBE2N from skin cells causes inflammation and immune response, which can be lessened with specific inhibitors.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

High-dose radiation speeds up aging in skin stem cells.

Suppressing ODC activity reduces tumor growth in hair follicles.

CXXC5 is a protein that prevents hair growth and could be a target for hair loss treatment.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

ETS2 is crucial in squamous cell carcinoma development and could be a therapeutic target.

FGF13 gene changes cause excessive hair growth in a rare condition.

Akt2 protein is essential for normal cell division in early mouse embryos.

E6/E7 oncogenes in hair follicles cause continuous hair growth by skipping the resting phase.

RXRα is crucial for proper immune response and links diet to immune function.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

Targeting ornithine decarboxylase can help prevent skin cancer.