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The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

The Shaven mutation in mice affects hair growth and causes a greasy coat due to abnormal lipid content.

Low-penetration genes might help personalize colorectal cancer prevention.

Super-enhancers controlled by pioneer factors like SOX9 are crucial for stem cell adaptability and identity.

Keratin 17 is crucial for cell growth in wound healing by aiding protein synthesis.

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

EZH2 is crucial for uterine gland development and female fertility.

Blocking EGFR in mice causes hair loss and skin changes.

Mouse skin has special cells in the epidermis that decrease with age and are linked to keratinocyte stem cells.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

Defective nuclear transport may cause gene expression changes in Progeria.

A genetic variant in the KRT25 gene causes tightly curled hair.

Mice with the naked gene have missing or abnormal hair cells.

A new therapy for a skin blistering condition has not been developed yet.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

The genes OVOL1 and OVOL2 are important for hair growth and may be involved in a type of skin tumor.

CAP1 helps Arabidopsis plants grow better under ammonium stress.

PP2Acα is essential for proper hair and skin development.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

Foxn1 helps skin cells mature by controlling a specific protein's activity.

The Apc gene is crucial for normal skin and thymus development.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

Turning off the Lhx2 gene in mouse embryos leads to slower wound healing and scars.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

Two new gene mutations cause a rare hair disorder.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Lower SMAD2/3 activation predicts more severe skin cancer.