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Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Inactivating both p53 and Rb genes in mice speeds up aggressive skin cancer development.

H3K4me3 helps control RSPO3 to influence hair growth and development.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Meis2 is essential for whisker development, independent of nerve involvement.

Targeting the HEDGEHOG-GLI1 pathway could help treat keloids.

Newly born mesenchymal cells quickly spread out in response to tissue tension during early development.

A mutation in the human hairless gene causes alopecia universalis.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

Collagen XVIII affects wound healing, hair growth, and bone development, with its absence speeding up processes and overexpression causing delays and abnormalities.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

Monilethrix is linked to a gene cluster on chromosome 12.

JAGGED1 could help regenerate tissues for bone loss and heart damage if delivered correctly.

The scraggly mutation causes hair loss and skin defects in mice.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

TSC2 is crucial for proper hair follicle development and patterning.

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

RXR-alpha is strongly expressed in both normal and psoriatic skin and may help in skin cell differentiation and hair growth.

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

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

p63 controls Satb1 to help skin develop properly.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

Dynlt3 is important for melanosome transport and skin coloration.

Two new gene mutations cause a rare hair disorder.

BMP signaling is essential for the development of touch domes.