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Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

Changes in KRT17 gene activity linked to wool production in Angora rabbits.

Pyruvate Kinase M2 helps hair grow by linking energy production and a key hair growth pathway.

Twist2 is essential for scarless skin healing and hair growth in mouse fetuses.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Acne patients have higher mTOR gene expression.

miR-29 is a key factor that accelerates aging.

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

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

Controlling cellular changes can enable safe rejuvenation without cancer risk.

GLABRA 2 controls ethylene production to help root hair growth during nutrient deficiency.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

HPV genes in mice improve ear tissue healing by speeding up skin growth and repair.

PRAME is often present in Paget disease and could help in diagnosis, but more research is needed.

FOXN1 gene variants cause low T cells and immune issues from birth.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

Mouse skin cells can become sperm-like cells in the lab.

Certain genes may promote longer root hairs in plants when phosphorus is low.

The G(S) alpha subunit gene may help start hair follicle growth in newborn mice.

Researchers created a new mouse model for studying scleroderma.

Different keratins have unique expression patterns in mouse skin cells.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

Two new gene mutations cause a rare hair disorder.