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Using polyethylenimine-DNA to deliver the hTERT gene can stimulate hair growth and may be useful in treating hair loss, but there could be potential cancer risks.

Two new gene mutations cause a rare hair disorder.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

DNA changes in tetraploid wheat improve root growth and nitrogen use.

High levels of ST14 and TMEFF1 proteins in ovarian cancer are linked to worse patient outcomes and may be a new treatment target.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

Gap junctions help control feather pattern formation by enabling cell communication.

Melanoma cells lose their ability to form tumors when placed in a zebrafish embryo environment.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

OR2AT4 helps reduce aging and cell damage in human skin cells.

The transcription factor Meis2 is essential for touch sensation and proper nerve development in touch receptors.

Overexpressing COX-2 in mice skin reduces skin tumor development.

Turning off the Lhx2 gene in mouse embryos leads to slower wound healing and scars.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

UBC13 and UBC22 enzymes are important for plant growth and development in Arabidopsis thaliana.

Retinoic acid changes skin cells to mucosal cells with goblet cells, needing TG2/Gh, Gbx1, and TGF-beta.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

Lack of functional CYLD in mice leads to early aging and cancer.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

Non-canonical Wnt signaling helps intestinal stem cells move to injury sites for tissue repair.

Truncated LTBP-1 disrupts TGF-beta signaling, affecting hair growth.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.