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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Hedgehog signaling is essential for normal sebaceous gland development and affects keratin 6a expression.

Injecting α-MSH made mice's hair turn black.

Adding a specific gene to skin cells can help treat skin disorders like psoriasis.

SQSTM1 gene issues may increase the risk of alopecia areata.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Researchers found specific genes in the part of hair follicles that could help treat hair disorders.

rRSPO1 protein boosts hair growth by activating a key signaling pathway.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

Mesenchymal stem cells and their secretome may offer a safe and effective treatment for systemic lupus erythematosus.

Genetic variations affecting skin structure play a key role in severe acne.

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

MED1 affects skin wound healing differently with age, speeding it up in young mice but slowing it in older mice.

miR-124 helps mouse hair follicle stem cells become nerve cells by blocking Ptbp1 and Sox9.

Human amniotic stem cell exosomes may effectively treat hair loss by promoting hair regrowth.

Adipose stem cells show common protein changes as they grow, especially involving S100A6.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

Collagen XVIII and Bmx tyrosine kinase are important for hair growth and skin cancer development.

S100A6 protein is linked to disease progression, especially in cancers.

Smad4 is important for healthy hair follicles because it helps produce a protein needed for hair to stick together and grow.

The LMNA mutation affects skin structure even in asymptomatic carriers.

The protein SLC1A3 is important for activating skin stem cells and is necessary for normal hair and skin growth in mice.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

BRG1 is essential for skin cells to move and heal wounds properly.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

Zfp157 is active in many mouse tissues during development and in specific adult cells.