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Glioblastoma cells can make androgens, which might help the tumor grow.

Mutations in claudin-1 and claudin-3 cause hair loss in baby mice.

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

The study found that Tourette Syndrome may be linked to certain immune system processes and synaptic signaling.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

Trichohyalin, a protein from pig tongue, was purified and found to have a filamentous structure.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

BI 2536 had limited effectiveness against several advanced cancers and caused significant side effects.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

SOCS1 and SOCS3 help control skin inflammation and are important for developing treatments for skin diseases.

3D cultures respond better to minoxidil, while 2D cultures respond better to DHT.

A combination of arginine silicate complex and magnesium biotinate improves hair and nail growth in rats.

IGFBP-5 likely plays a key role in goat hair growth.

Boosting β-catenin signaling in certain skin cells can enhance hair growth.

BMP signaling affects hair color by interacting with the MC-1R pathway.

GPC1 is important for hair growth by helping blood vessels form around hair follicles.

MJ04, a new compound, effectively promotes hair growth and is a potential topical treatment for hair loss.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

1,25-(OH)2D3 helps hair grow by blocking certain harmful signals.

DMBT1 and galectin-3 may help suppress epithelial skin cancer.

SOCS3 treatment can prevent hair loss by stopping harmful immune responses.

Trichocytic cytokeratins are found in hair, nails, tongue, and thymus cells, showing complex regulation in tissue development.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

Human hair keratin has a 40% α-helix structure that changes to a random coil in 8 M urea.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

NM2 and RLC phosphorylation are essential for normal inner ear hair cell function.

The research found changes in gene expression related to cell death in mouse skin that help understand hair follicle development and skin health.