Robert E. Maxson

Research.com Recognitions

• 2013 - Fellow of the American Association for the Advancement of Science (AAAS)

Overview

Best Publications

• Tissue origins and interactions in the mammalian skull vault.

  Xiaobing Jiang;Sachiko Iseki;Robert E. Maxson;Henry M. Sucov

  995
  Citations

• Germline Competent Embryonic Stem Cells Derived from Rat Blastocysts

  Ping Li;Chang Tong;Ruty Mehrian-Shai;Li Jia

  973
  Citations

• Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation.

  Ichiro Satokata;Liang Ma;Hayato Ohshima;Marianna Bei

  920
  Citations

• Cyclic dermal BMP signalling regulates stem cell activation during hair regeneration

  Maksim V. Plikus;Julie Ann Mayer;Damon de la Cruz;Ruth E. Baker

  803
  Citations

• 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;Liang Ma

  788
  Citations

• Recent advances in craniofacial morphogenesis.

  Yang Chai;Robert E. Maxson

  691
  Citations

• Integration of FGF and TWIST in calvarial bone and suture development.

  David P. C. Rice;Thomas Åberg;Yan-Shun Chan;Zequn Tang

  461
  Citations

• Generation of a prostate epithelial cell-specific Cre transgenic mouse model for tissue-specific gene ablation.

  Xiantuo Wu;Jian Wu;Jiapeng Huang;William C. Powell

  447
  Citations

• Expression and Organization of Histone Genes

  Robert Maxson;Ronald Cohn;Larry Kedes;Timothy Mohun

  365
  Citations

• Conditional inactivation of Fgf4 reveals complexity of signalling during limb bud development

  Xin Sun;Mark Lewandoski;Erik N. Meyers;Yi-Hsin Liu

  344
  Citations

• Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.

  Andrew O.M. Wilkie;Zequn Tang;Navaratnam Elanko;Sinead Walsh

  329
  Citations

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

  Yi Hsin Liu;Ramendra Kundu;Lanying Wu;Wen Luo

  276
  Citations

• Conditional deletion of MSX homeobox genes in the uterus inhibits blastocyst implantation by altering uterine receptivity

  Takiko Daikoku;Jeeyeon Cha;Xiaofei Sun;Susanne Tranguch

  264
  Citations

• Mesenchymal origin of hepatic stellate cells, submesothelial cells, and perivascular mesenchymal cells during mouse liver development

  Kinji Asahina;Shirley Y. Tsai;Peng Li;Mamoru Ishii

  261
  Citations

• Regulation of Msx-1, Msx-2, Bmp-2 and Bmp-4 during foetal and postnatal mammary gland development

  D.J. Phippard;S.J. Weber-Hall;P.T. Sharpe;M.S. Naylor

  241
  Citations

• Targeted Disruption in Murine Cells Reveals Variable Requirement for Smad4 in Transforming Growth Factor β-related Signaling

  Christian Sirard;Sammy Kim;Christine Mirtsos;Paul Tadich

  241
  Citations

• The Molecular Basis of Boston-Type Craniosynostosis: The Pro148→His Mutation in the N-Terminal Arm of the MSX2 Homeodomain Stabilizes DNA Binding without Altering Nucleotide Sequence Preferences

  Liang Ma;Serge Golden;Linda Wu;Rob Maxson

  241
  Citations

• Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis

  Amy E. Merrill;Elena G. Bochukova;Sean M. Brugger;Mamoru Ishii

  231
  Citations

• Orphons: Dispersed genetic elements derived from tandem repetitive genes of eucaryotes

  Geoffrey Childs;Rob Maxson;Ronald H. Cohn;Larry Kedes

  231
  Citations

• Mutations in TCF12 , encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis

  Vikram P Sharma;Aimée L Fenwick;Mia S Brockop;Mia S Brockop;Simon J McGowan

  219
  Citations