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Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

A woman with EMS showed unusual skin mucinosis without the typical hard skin syndrome, suggesting EMS can cause skin mucinosis.

Red light increases hair follicles and ATP in mouse skin.

Smad4 is crucial for muscle repair, especially in aging, by promoting cell growth over differentiation.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Minoxidil sulfate relaxes muscle by increasing potassium flow, making it a unique muscle relaxer.

A gene mutation in mice causes skin defects and early death.

MLPH helps hair grow by activating IGF-1 signaling in hair cells.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Some leukemia treatments can cause skin reactions similar to keratosis pilaris.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

Lipin-1 is important for skin cell differentiation and skin barrier function.

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

Mesenchymal stem cells from laser-assisted liposuction are as effective and safe as those from conventional liposuction for cell therapy.

Using fat-derived stem cells with the drug meglumine antimoniate can help control skin disease and reduce parasites in mice with leishmaniasis.

Ishige sinicola extract may help prevent muscle atrophy through its antioxidant and anti-inflammatory effects.

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

Lrig1 marks a unique group of stem cells in mouse skin that can become different skin cell types.

Msx-2 gene removal speeds up skin wound healing in mice.

c-Kit is important for heart regeneration and cancer development.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

c-Myc activation in mouse skin increases sebaceous gland growth and affects hair follicle development.

Mitochondriopathy may cause eyelash loss.