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Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Human basal cell carcinomas and squamous cell carcinomas have unique gene expression patterns not fully mirrored in mouse models.

Tofacitinib is a promising treatment for children with rheumatic diseases.

Interferon, especially alfa interferon, is an effective treatment for cutaneous T-cell lymphoma with manageable side effects.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

Targeting regulatory T cells may help treat age-related diseases.

T-regulatory cells are important for skin health and can affect hair growth and reduce skin inflammation.

Lower levels of MYLK and CALD1 in bladder cancer and osteosarcoma are linked to worse survival rates.

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

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

CD34 is crucial for skin tumor development in mice.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

Thyrotropin-Releasing Hormone helps heal wounds in frog and human skin.

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

COVID-toes show a unique immune response over time, different from vaccine-related chilblains.

TP0427736 may help treat hair loss by blocking a specific protein and promoting hair growth.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

A gene variant causes a skin and hair disorder by disrupting protein balance.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Treg cells help repair and regenerate tissues by interacting with local cells.

A new mouse mutation causes skin and hair defects due to a gene change.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

The assay effectively identifies compounds that affect immune cell activation.

A mutation in the VDR gene affects hair cycling without needing ligand binding.