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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Diet changes can protect against harmful environmental effects on fetal development.

Mice lacking a key DNA methylation enzyme in skin cells have a lower chance of activating stem cells necessary for hair growth, leading to progressive hair loss.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Eph receptors and ephrins may be promising targets for treating diseases, but more understanding is needed for effective and safe therapies.

Blocking interferon-gamma might help treat various autoimmune diseases.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

There might be a specific histone code for cellular quiescence, but more research is needed.

A brain-produced steroid causes increased scratching in mice with a skin condition similar to eczema.

Trichocyte filaments have a low-density core and may include proteins for hair structure.

Trichohyalin granules help inner root sheath cells in hair follicles harden by integrating with keratin filaments.

The cuneate nucleus has two main neuron types: relay neurons and interneurons.

Trichohyalin is a protein in hair follicles that helps form hair filaments.

Sheet formation is key to macrofibril structure differences in wool.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

Trichohyalin helps in hair and skin cell structure and function by binding calcium and linking proteins.

Involucrin helps strengthen the inner parts of human hair.

Trichohyalin is a versatile protein involved in hair and skin structure.

Oxidized trichocyte keratin has a helical dislocation in its structure.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

μ-Crystallin may help hair growth by affecting thyroid hormone levels in mouse hair follicles.

Actin filaments help stabilize and integrate cell membranes during transfer.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Understanding how fetal wounds heal could help improve healing in adults.

A unique hair tumor with a rippled pattern was identified, showing incomplete differentiation and unusual cell arrangements.

Defects in certain proteins cause major heart abnormalities during early development.

Mast cell and nerve fiber interactions in mouse skin change with the hair cycle.

S100A3 protein is mainly found in specific parts of human hair cells.