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ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.

PTHrP regulates various normal body functions, including bone development, skin, and muscle function.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

PROTACs show promise in cancer treatment by effectively degrading specific harmful proteins.

Mutations in the KRT85 gene cause hair and nail problems.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

A specific gene mutation causes a severe skin disorder in a family.

Two new gene clusters important for hair formation were found on human chromosome 11.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Plasmalogens activate a channel in cells that may stimulate hair growth.

miR-5110 affects alpaca pigmentation by altering specific gene expressions.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

Two new gene clusters important for hair formation were found on human chromosome 11.

QLT0267 stops hair follicle cell growth and movement.

Grasp protein helps maintain skin health after UVB exposure.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Keratinocyte cytokines and genetic variations influence the development of moles and skin pigmentation.

CK 5/6 expression in breast cancer is linked to negative hormone receptor status and higher tumor grade.

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

Pig skin cells can turn into mesodermal cells but lose their ability to become neural cells.

Calcium is crucial for skin development and healing.

Inactivating β-catenin is essential for chick retina regeneration.

Plet-1 protein helps hair follicle cells move and stick to tissues.

uPA helps hair follicle cells grow.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

ALRN-6924 may prevent hair loss caused by chemotherapy.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.