Wen Luo

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

Ethylin Wang Jabs, Ulrich Müller, Xiang Li et al. · Cell · 1993 · 678 citations

Sclerostin, Developmental Biology, Genetic Disorder +6

Premature suture closure and ectopic cranial bone in mice expressing Msx2 transgenes in the developing skull.

Y H Liu, Ramendra Kundu, Linda Wu et al. · Proceedings of the National Academy of Sciences · 1995 · 223 citations · Full text

Sclerostin, Premature Suture Closure, Neural Stem Cell +24

Msx2Gene Dosage Influences the Number of Proliferative Osteogenic Cells in Growth Centers of the Developing Murine Skull: A Possible Mechanism forMSX2-Mediated Craniosynostosis in Humans

Yi‐Hsin Liu, Zequn Tang, Ramendra K. Kundu et al. · Developmental Biology · 1999 · 203 citations

Sclerostin, Developmental Biology, Bone Morphogenic Protein +14

Myomaker, Regulated by MYOD, MYOG and miR-140-3p, Promotes Chicken Myoblast Fusion

Wen Luo, Erxin Li, Qinghua Nie et al. · International Journal of Molecular Sciences · 2015 · 111 citations · Full text

Altered metabolome and microbiome features provide clues in understanding irritable bowel syndrome and depression comorbidity

Lijuan Han, Ling Zhao, Yong Zhou et al. · The ISME Journal · 2021 · 111 citations · Full text