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Finasteride affects prostate development differently in male and female Mongolian gerbils.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

GRF is not safe for tubal occlusion.

Geriatric Julia Creek dunnarts often suffer from reproductive and skin diseases, impacting conservation efforts.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

EMT and metabolic pathways help cancer cells resist treatment and spread.

Human hair follicles can provide stem cells for regenerative medicine.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

COL17A1 is crucial for preventing hair graying and loss by supporting hair and pigment stem cells.

Antihepcidin antibodies may treat inflammation-induced anemia by improving iron metabolism.

BMAL1 controls skin cell growth and UV damage risk, peaking at night.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

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.

A combined approach is needed to fully understand adult stem cells, with genetic lineage-tracing being crucial.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Age, health conditions, race, and gender affect COVID-19 risk.

Dermal adipose tissue in mice can change and revert to help with skin health.

Targeting the Smoothened receptor shows promise for treating certain cancers.

Certain immune cells in the skin release a protein that stops hair growth by keeping hair stem cells inactive.

Phospholipase Cδ1 is crucial for normal skin and hair development.

Metabolic signals and cell shape influence how cells develop and change.

Matriptase is crucial for skin barrier, hair growth, and may contribute to skin cancer.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

NEDD4 and NEDD4L help control intestinal stem cells and prevent tumors by breaking down the LGR5 receptor.

Afatinib often causes skin problems that need proactive management.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

Hox genes are crucial for development and tissue maintenance, affecting structures and functions throughout life.