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Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

Adding TERT and BMI1 to certain skin cells can improve their ability to create hair follicles in mice.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

A specific combination of chemicals effectively expands genetically modified skin cells for potential use in skin therapy.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

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

Hox genes control hair follicle stem cell regeneration in different body regions.

Dermal EZH2 controls skin cell growth and differentiation in mice.

Truncated LTBP-1 disrupts TGF-beta signaling, affecting hair growth.

CDP is crucial for lung and hair follicle cell development.

New bio-ink can print complex tissues and organs.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

LHX2, with other markers, can identify hair placodes in rats.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

TCF/Lef1 activity is essential for proper skin cell development and renewal.

Follistatin and LIN28B together improve the ability of inner ear cells in mice to regenerate into hearing cells.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

GLI2 increases follistatin production in human skin cells.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Glucocorticoids and thyroid hormones together are essential for fetal fat development.

Hair follicle stem cells help maintain skin health by moving to and supporting the skin's surface layers.

Bexxar treatment led to a high response rate in patients with advanced-stage, treatment-resistant follicular lymphoma.

Hoxc13 is essential for hair growth and follicle development.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.