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The new method using gene-modified stem cells and a 3D printed scaffold improved skin repair in mice.

Mutations in the HOXC13 gene cause hair and nail development issues.

Adult esophageal cells can start to become like skin cells, with a key pathway influencing this change.

BcFLA1 protein is crucial for root hair growth in response to low phosphate in Brassica carinata.

The N-K GM Series offers a new method to reduce aflatoxin poisoning and cancer, improving health and saving costs in affected regions.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

p63 controls Satb1 to help skin develop properly.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

Knocking out the FGF5 gene in sheep increased wool production and hair-follicle density.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

SLC3A2 is crucial for hair follicle stem cell function and hair growth.

Gamma-ray exposure improves genome editing efficiency in mice using the i-GONAD method.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

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

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Gentile di Puglia sheep have finer wool and more lanolin than Sarda sheep.

MiR-23b and miR-133 affect sheep hair growth by targeting specific genes.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

The treatments stopped hair regrowth in mice.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

SGK3 is essential for proper hair growth and health.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Ablative fractional laser treatment nearly matches the gene reduction effects of topical vismodegib in skin cancer.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Scube3 gene affects mouse embryo growth in multiple areas, but needs more research.

A new gene mutation is linked to monilethrix in the studied family.