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Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

Fibroblasts from healthy donors can prevent changes seen in recessive epidermolysis bullosa simplex.

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

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

NIR-II imaging effectively tracked stem cells that helped repair facial nerve defects in rats.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Resveratrol activates the Nrf2 pathway in human skin, significantly increasing the production and distribution of the antioxidant glutathione.

PRF lysates reduce inflammation in cancer cells and boost immune response in healthy oral cells.

The study provides exploratory findings on miRNA changes in female hair loss.

The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

Calcium signaling in skin cells is crucial for communication and regeneration.

5alpha-reductase 2 is crucial for proper male brain development and sexual differentiation.

BAF200 is essential for proper heart and coronary artery formation.

Certain circular RNAs may regulate wool follicle growth in sheep.

Certain miRNAs might be involved in a hair loss condition called frontal fibrosing alopecia and could possibly help in its diagnosis.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Low-level red light therapy can shorten eye length in some myopic children.

Low-level laser therapy reduces symptoms and inflammation in frontal fibrosing alopecia.

Two gene areas linked to male pattern baldness found, more research needed.

Gene variation affects prostate issues and hair loss.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.