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The transition from growth to regression in Cashmere goat hair follicles involves changes in expression of genes related to keratin and cell differentiation.

Constant-release melatonin reduces SOX21 gene expression in goats during the hair follicle resting phase.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

The K5 promoter controls gene expression in skin cells, with specific DNA segments crucial for targeting and regulation.

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

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

Certain gene variations increase the risk of alopecia areata in Koreans.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

circCFAP20DC helps goat ovarian cells grow, aiding follicle development.

Defective nuclear transport may cause gene expression changes in Progeria.

Fox genes are important for hair growth and development in cashmere goats.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Blocking CXXC5 speeds up diabetic wound healing by improving blood vessel growth and skin repair.

A specific RNA in cashmere goats helps improve hair growth by interacting with certain molecules.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

The genetic variation in the KAP13-3 gene may affect cashmere fiber traits in Liaoning goats.

Overexpression of ΔNLef1 in mouse skin leads to hair loss, cysts, and skin tumors.

The rs1128977 gene variant may affect cholesterol and body measurements.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

pCLCA2 protein may help maintain skin structure and function.

C/EBPalpha and C/EBPbeta are crucial for normal skin and oil gland cell development in adult mice.

p21waf1/cip1 and p27kip1 help in hair follicle differentiation in rats.