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Altering maternal cortisol during pregnancy can improve wool growth in Merino sheep.

The engineered skin substitute helped grow skin with hair on mice.

Different ectodermal organs like hair and feathers regenerate differently, with specific stem cells and signals involved in their growth and response to the environment.

Neural crest-derived progenitor cells in the cornea could help treat corneal issues without transplants.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

Basement membrane changes are crucial for hair follicle development.

Epidermal growth factor helps hair stem cells grow by activating specific cell pathways.

Topiramate impairs gene transmission in zebrafish, while Ginkgo biloba reduces harmful effects of high β-catenin levels.

A simple enrichment program improves health and reproduction in Calomys callosus.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

The new method makes it easier to study the whole cochlea from newborn mice and rats in the lab.

The BMP2 gene is more active in the early growth phase of Cashmere goat hair and may affect hair regeneration and textile production.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

miR-200a reduces goose fibroblast growth by targeting PITX2 in the Wnt pathway.

EGF helps secondary hair follicles grow in young gray goats.

New bio-ink can print complex tissues and organs.

EBF1 controls hair type and length.

SOX9 helps determine stem cell roles by interacting with DNA and proteins that control gene activity.

Certain RNA molecules are important for the development of wool follicles in sheep.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

New mouse models help study melanocytic cells for melanoma research.

Engineered exosomes with EGF and FGF improve hair growth in mice with hair loss.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.