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Mitochondrial Complex I reduces inflammation and increases bone breakdown by affecting certain immune cells.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Calcium channels are vital for normal skin function and their dysfunction can lead to skin issues.

MESTSV is a rare tumor that is mostly benign but needs long-term monitoring due to potential recurrence.

rTMS may help treat trichotillomania in some patients.

AZD6244 treatment causes skin aging effects by depleting skin stem cells.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

Mice that can regenerate tissue have cells that pause in the cell cycle, which is important for healing, similar to axolotls.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

DNMT3A is crucial for healthy skin and hair growth.

The sensor accurately measures thallium ions in solutions with high selectivity.

Twist1 helps maintain important features of cells crucial for hair growth by working with Tcf4 and β-catenin.

Feather patterns in birds are shaped by signaling interactions and cell movements, with EDA/EDAR crucial for pattern formation.

The Gsdma3 gene is essential for normal hair development in mice.

Certain genes control the color of human hair by affecting pigment production.

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

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

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

Activating PKM2 and Wnt/β-catenin signaling together can potentially enhance hair growth and could be a treatment for hair loss.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Mouse touch-sensitive nerve cells adjust their connections based on competition with other similar cells.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

The study found that p63 needs signals from morphogens to help skin cells differentiate properly.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

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

Using polyethylenimine-DNA to deliver the hTERT gene can stimulate hair growth and may be useful in treating hair loss, but there could be potential cancer risks.