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PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

A mutation in the Sgkl gene causes defective hair growth in mice.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

The FOS gene helps hair growth in Tan sheep.

KRT17 may be a new target for endometrial cancer treatment because it helps cancer cells move and form new blood vessels.

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

Wnt10b helps hair follicle cells mature and produce pigment.

BMAL1 controls skin cell growth and UV damage risk, peaking at night.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

RNase L hinders hair follicle regeneration by altering immune signals.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

RANKL improves the immune response against herpes simplex virus by enhancing T cell activation and could help develop better treatments or vaccines.

Multiple mouse desmoglein 1 isoforms have distinct roles in skin and hair development.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

Melatonin given to pregnant rabbits improved their babies' fur quality.

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

Mutations in the LIPH gene cause woolly hair in a child.

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.

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.

XIST RNA helps regenerate hair follicles by targeting miR-424 and activating hedgehog signaling.

Krox20 (Egr2) is important for the function of epithelial stem cells.

NEDD4 and NEDD4L help control intestinal stem cells and prevent tumors by breaking down the LGR5 receptor.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Wnt signaling is crucial for Hedgehog-driven skin tumor growth.

BMI1 is essential for preventing hair greying and maintaining hair color.