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S-1 treatment led to a complete response in pancreatic cancer with manageable side effects.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Meis1 is crucial for skin health and tumor development.

FKBP10 and FBN2 are key proteins for hair growth in cashmere goats.

Ritlecitinib effectively treats severe Alopecia Areata by reducing harmful immune activity in the skin.

Key genes and RNA networks regulate hair growth and follicle density in Rex rabbits.

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

Patients with RASopathies have a higher risk of autoimmune disorders and should be routinely screened.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

Nitrate helps plants manage phosphate uptake and starvation responses through NIGT1 proteins.

Rapamycin treatment helps with mitochondrial disease by reducing PKC levels.

Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

LSD1 and HSP90 help heal skin wounds by changing hair follicle stem cells' metabolism.

ROR2 is essential for hair follicle stem cell renewal and maintenance.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Unique fat cells near fibrotic areas contribute to systemic sclerosis progression.

SARS-CoV-2 may worsen IPF due to shared genes and pathways, suggesting potential drug targets.

PSAT1 is key for hair growth and stem cell function in cashmere goats.

Increasing SSAT makes skin more prone to cancer.

Planarians regenerate using conserved gene expression mechanisms, with runt-1 crucial for cell type specification.

Intramuscular injection of 131I is a safe and effective way to induce hypothyroidism in rats without harming muscle tissue.

Rat liver stem cells can grow into organoids and help treat liver diseases.

DA-9401 helps protect rat testis from finasteride damage.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.