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The mutation causing Hutchinson-Gilford progeria syndrome leads to severe skin problems and early death in mice.

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

Erythropoietin overexpression disrupts hair growth and fat formation in mice.

m6A-circHECA helps stem cells become hair follicles in cashmere goats.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

ARHGEF3 is essential for proper hair follicle development.

PrrH sRNA controls pyochelin production in *Pseudomonas aeruginosa*.

A gene mutation in mice causes permanent hair loss and skin issues.

TCF/Lef1 activity is essential for proper skin cell development and renewal.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

Plet-1 protein helps hair follicle cells move and stick to tissues.

Lef1 helps adult skin cells maintain their ability to heal wounds and regenerate hair, but the study's methods and conclusions have been questioned.

Certain liver diseases respond well to specific treatments and have varying risks for liver cancer.

HAP stem cells can repair nerves, grow hair follicle nerves, and become heart muscle cells, making them useful for regenerative medicine.

High-dose interferon is effective for chronic hepatitis C but often causes flu-like symptoms.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

The HR protein helps hair grow by blocking a hair growth inhibitor, aiding in hair follicle regeneration.

Hair follicle cells can help keep embryonic stem cells undifferentiated.

LPA 4 helps control blood and lymph vessel development in zebrafish.

H2AK119ub helps keep hair follicle stem cells in a resting state, preventing early aging.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Hhip-Cre effectively targets dermal papilla cells for gene manipulation in hair biology.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Human placenta hydrolysate reduces inflammatory pain and nerve damage in mice.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.