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Collagen XVIII and Bmx tyrosine kinase are important for hair growth and skin cancer development.

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Acidic keratin genes are on CFA9 and basic keratin genes are on CFA27 in dogs.

The hexosamine pathway helps maintain healthy skin by affecting the skin's structure and possibly increasing hair follicle stem cells.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.

Alopecia X in Pomeranians is likely genetic, not environmental.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

OCT4B1 and SOX-2 levels are higher in Crohn's and ulcerative colitis patients, possibly aiding tissue repair.

A 12-year-old girl's hair loss was linked to a rare genetic condition called ALX4-related frontonasal dysplasia.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Nestin-expressing progenitor cells become outer root sheath keratinocytes.

The newborn's skin blistering is due to a genetic condition called epidermolytic hyperkeratosis.

A rare skin condition was identified and planned for treatment in an elderly man.

Scientists found cells in hair that are key for growth and color.

Skin changes in Pseudoxanthoma elasticum patients can indicate the severity of related health issues.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

Different PADI isoforms help cells develop diverse functions.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

GLI2 increases follistatin production in human skin cells.

The hairless gene mutation causes baldness by disrupting hair follicle structure.

A specific gene mutation causes severe skin and nail issues and hair loss.

RXR-alpha is strongly expressed in both normal and psoriatic skin and may help in skin cell differentiation and hair growth.