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hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

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

Enzymes that change arginine to citrulline are important for skin barrier and hair formation, and their malfunction can lead to skin conditions and hair disorders.

A specific RNA in cashmere goats helps improve hair growth by interacting with certain molecules.

MC4R gene variants not linked to female hair loss.

Human hair follicles contain a complex network of prostanoid receptors that may influence hair growth.

Tudor-SN is important for immune cells, and polyamines can promote hair growth.

YAP1 is important for skin regeneration and may affect skin disorder treatments.

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

The HCR gene contributes to psoriasis risk.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

GLABRA2 gene controls root-hair growth by regulating phospholipid signaling.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

A new DSG4 gene mutation causes hair defects in a young girl.

XMU-MP-1 stops cell growth in a human mini-organ and reduces the effectiveness of the chemotherapy drug paclitaxel.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Blocking the Mitochondrial Pyruvate Carrier causes stress in hair follicles, which can be reduced by an ISR inhibitor.

Pexidartinib often causes liver issues and fatigue, especially in women.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

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

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

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

The conclusion is that a treatment called cp-asiAR can reduce hair loss and promote hair growth, making it a potential new therapy for androgenetic alopecia.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.