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The gelatin/β-TCP scaffold with nanoparticles improves wound healing and skin regeneration.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.

Hair follicle cells help maintain and support stem cells and blood cell formation.

Melatonin affects when and how goat hair follicle genes turn on and off during growth cycles.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

A new method improves protein extraction from hair, helping identify potential biomarkers for fetal growth issues.

EGF affects hair and skin development.

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

Ten miRNAs may play key roles in starting secondary hair follicle development in sheep foetuses.

BAF200 is essential for proper heart and coronary artery formation.

miRNAs in the Dlk1-Gtl2 region may improve lamb fur quality.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

N6-methyladenosine affects hair follicle development differently in Rex and Hycole rabbits.

Dermal EZH2 controls skin cell development and hair growth in mice.

Key genes and pathways influence wool traits in Merino sheep.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

LED therapy can safely and effectively regrow eyebrows in people with frontal fibrosing alopecia.

Sox2 controls hair color by affecting pigment production in hair follicles.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

The Foxn1 gene is essential for normal nail and hair development.

Loss of Fz6 disrupts hair follicle and associated structures' orientation.

Researchers found four distinct fibroblast types in human skin, which could help in treating wounds and fibrotic diseases.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

A new type of nerve cell involved in itch perception was discovered.

New lipid/fiber microplexes improve mRNA therapy for degenerative diseases by enhancing cell function and treatment effectiveness.

Human hair follicles produce and respond to erythropoietin, helping protect against stress.

FFA patients have fewer melanocytes and thinner skin compared to others.