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The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Certain genes contribute to stronger hooves in barefoot racing horses.

Gasdermin A3 overexpression in skin causes inflammation and hair loss.

Stem cell therapy affects 15 key genes in rats with diabetes-related erectile dysfunction.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Spt4 and Spt6 are essential for fat cell development.

EDA2R gene linked to hair loss.

FGFR2 signaling controls Merkel cell formation in different skin regions.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

ZmSPL10, ZmSPL14, and ZmSPL26 genes are essential for forming maize structures needed for pollen capture and kernel production.

61 functional keratin genes were identified in dogs and horses, leading to updated gene annotations.

Three genes in Arabidopsis are important for plant growth and development by affecting sugar attachment to proteins.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

A new gene mutation causes a rare type of hair loss.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Exosomes from fat stem cells can reduce fat cell formation.

A new gene, JMJD1C, may affect testosterone levels in men.

Steroid 5α-reductase evolved from protists and diversified in eukaryotes, with specific roles in mammals and plants.

MicroRNA-200 prevents sebaceous gland development by inhibiting SOX9 and cell cycle progression.

Retinoic acid and DMSO improve gene delivery to mouse skin for potential hair and skin disease treatment.

Exosomes from certain stem cells can promote hair growth and counteract hair loss caused by hormones by regulating growth factors and other cellular signals.

Mutations in keratin genes cause cell fragility and various skin disorders.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

DNMT3A is crucial for healthy skin and hair growth.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Ectodysplasin signaling is crucial for skin appendage development, requiring specific doses and durations.