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SK2 channels help control sensory signals in rat muscle spindles and hair follicles.

The tool iCOUNT helps understand how stem cells divide and affect tissue development and repair.

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

Keratin 15 helps keep skin cells in a young, undifferentiated state.

LncRNA RP11-818024.3 helps hair growth and recovery in hair loss by boosting cell survival and reducing cell death.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

PIEZO1 helps keep hair follicle stem cells inactive, affecting hair growth.

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

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Wnt/β-catenin signaling is crucial for cell fusion in placental development.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

The QuantAnts machines can find cancer markers and create CRISPR targets for them.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Scientists created a detailed map of gene activity in different parts of human hair follicles.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

The calcineurin/NFAT pathway plays a significant role in the development and growth of a type of skin cancer called cutaneous squamous cell carcinoma.

PROTACs offer a new, precise way to treat cancer by breaking down harmful proteins.

Loss of Rap1 protein speeds up heart aging in mice.

CYP11A1 is crucial for skin health and disease by producing important steroids.

Researchers found a new mutation causing total hair loss from birth.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

Keratin-associated proteins are part of the developing hair fiber cuticle.

Precise objectives can improve student achievement in health education.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

The WIF1 gene is crucial for hair growth in Angora rabbits.