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IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

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

Lymphocytes, a type of immune cell, are crucial for wound healing as they help remodel damaged areas and reduce inflammation.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.

Disrupting Bcl-xL in mice reduces skin cancer risk.

ERK activation spreads between cells, influencing cell division and wound healing.

Mouse keratin 6 genes evolved independently from human ones and are regulated differently.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Matrix effects in LC-MS can be managed but not completely avoided.

Drugs that block GSK-3 show promise for treating various diseases.

Laminin 332 is essential for normal skin cell behavior and structure.

SMAD4 is crucial for muscle repair in young adults but not in aged mice.

Akt2 and SGK3 are both important for normal hair growth and development.

Early treatment with the right dose of stem cells can reduce lupus symptoms.

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

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Mast cells might contribute to hair loss by causing skin thickening.

β‐thymosins, especially thymosin β4, help in heart protection, wound healing, and hair growth by stabilizing actin in cells.

Keratinocyte cytokines and genetic variations influence the development of moles and skin pigmentation.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Antizyme reduces tumor growth and normalizes skin cell development affected by MEK.

Three molecular subtypes of advanced skin T-cell lymphoma were identified, with potential biomarkers for predicting treatment response and disease progression.

Mouse models help target specific genes in lymphatic cells for research.

The African spiny mouse heals skin without scarring due to different protein activity compared to the common house mouse, which heals with scarring.

Food deprivation increases MST enzyme in the brain, possibly affecting energy balance.

Researchers created a new mouse model for studying scleroderma.

Proteolytic activity in mouse skin changes with hair cycle stages, peaking in early anagen.