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The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

New mutations in the hairless gene may cause hair loss and affect bone development.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

A truncated protein linked to breast cancer may change cell adhesion.

Certain microRNAs are more common in balding areas and might be involved in male pattern baldness.

High TSPEAR levels in colorectal cancer predict worse outcomes.

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.

GATA6 is important for maintaining and differentiating cells in a key area of human skin.

Researchers created a new mouse model for studying scleroderma.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

TAp63 and NRF2 work together to manage oxidative stress, preventing premature aging and aiding skin functions.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

Controlling cellular changes can enable safe rejuvenation without cancer risk.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

Some thymic peptides can increase human hair growth, while others may inhibit it.

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

Kdm6b is crucial for skin cell differentiation.

Identified genes linked to male-pattern baldness may help develop new treatments.

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

ZmSPL10, ZmSPL14, and ZmSPL26 genes are essential for forming maize structures needed for pollen capture and kernel production.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

MPA increases cancer spread by boosting Eph A2 activity.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

The UHS promoter is specific to mouse hair follicles.