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The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Some cancer treatments cause different types of hair loss, but scalp cooling can help prevent it.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

Ectodysplasin-A1 is crucial for developing hair, teeth, and glands.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

PP2Acα is essential for proper hair and skin development.

ILK is essential for skin development, pigmentation, and healing.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Hedgehog signaling can create new hair follicles but may also cause tumors.

Lack of functional CYLD in mice leads to early aging and cancer.

Wnt signaling is crucial for skin development and hair growth.

Three dogs with a rare skin condition improved with treatment.

Lef1 helps adult skin cells maintain their ability to heal wounds and regenerate hair, but the study's methods and conclusions have been questioned.

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

Overexpression of E2F1 can lead to skin tumors and disrupt hair growth.

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

Brindled mice show abnormal catecholamine neuron development due to copper deficiency.

The hamartoma is an abnormal hair growth with limited development in the upper hair follicle.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

Abnormal activation of hair follicle stem cells and Wnt/β-catenin signaling contributes to sebaceous neoplasms.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Mice without certain skin proteins had abnormal skin and hair development.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Early over-expression of FoxN1 harms immune and skin development.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Congenital alopecia in domestic animals is rare and involves abnormal hair follicle development, needing better understanding and classification.

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

Rat vibrissa follicles are useful for studying hair growth cycles, especially the transition from pro-anagen to anagen.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.