MaryAnn Weis

Overview

Best Publications

• CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta.

  Roy Morello;Terry K. Bertin;Yuqing Chen;Yuqing Chen;John Hicks

  553
  Citations

• Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta

  Wayne A Cabral;Weizhong Chang;Aileen M Barnes;MaryAnn Weis

  544
  Citations

• Deficiency of Cartilage-Associated Protein in Recessive Lethal Osteogenesis Imperfecta

  Aileen M. Barnes;Weizhong Chang;Roy Morello;Wayne A. Cabral

  384
  Citations

• Homozygosity for a Missense Mutation in SERPINH1, which Encodes the Collagen Chaperone Protein HSP47, Results in Severe Recessive Osteogenesis Imperfecta

  Helena E. Christiansen;Ulrike Schwarze;Shawna M. Pyott;Abdulrahman AlSwaid

  377
  Citations

• Articular cartilage collagen: an irreplaceable framework?

  David R. Eyre;Mary Ann Weis;Jiann Jiu Wu

  304
  Citations

• Excessive transforming growth factor-β signaling is a common mechanism in osteogenesis imperfecta

  Ingo Grafe;Tao Yang;Stefanie Alexander;Erica P Homan

  293
  Citations

• Advances in collagen cross-link analysis

  David R. Eyre;Mary Ann Weis;Jiann Jiu Wu

  280
  Citations

• CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta.

  Dustin Baldridge;Ulrike Schwarze;Roy Morello;Jennifer Lennington

  252
  Citations

• HIF-1α metabolically controls collagen synthesis and modification in chondrocytes

  Steve Stegen;Kjell Laperre;Guy Eelen;Gianmarco Rinaldi

  242
  Citations

• Spondylocheiro Dysplastic Form of the Ehlers-Danlos Syndrome—An Autosomal-Recessive Entity Caused by Mutations in the Zinc Transporter Gene SLC39A13

  Cecilia Giunta;Nursel H. Elçioglu;Beate Albrecht;Georg Eich

  234
  Citations

• Interaction of fibroblast growth factor and C-natriuretic peptide signaling in regulation of chondrocyte proliferation and extracellular matrix homeostasis

  Pavel Krejci;Bernard Masri;Vincent Fontaine;Pertchoui B. Mekikian

  232
  Citations

• Lack of Cyclophilin B in Osteogenesis Imperfecta with Normal Collagen Folding

  Aileen M. Barnes;Erin M. Carter;Wayne A. Cabral;MaryAnn Weis

  202
  Citations

• Location of 3-hydroxyproline residues in collagen types I, II, III, and V/XI implies a role in fibril supramolecular assembly.

  Mary Ann Weis;David M. Hudson;Lammy Kim;Melissa Scott

  196
  Citations

• Lysyl Oxidase Activity Is Required for Ordered Collagen Fibrillogenesis by Tendon Cells

  Andreas Herchenhan;Franziska Uhlenbrock;Pernilla Eliasson;MaryAnn Weis

  185
  Citations

• Receptor Tyrosine Kinases Activate Canonical WNT/β-Catenin Signaling via MAP Kinase/LRP6 Pathway and Direct β-Catenin Phosphorylation

  Pavel Krejci;Pavel Krejci;Anie Aklian;Marketa Kaucka;Eva Sevcikova

  176
  Citations

• Bone Collagen: New Clues to Its Mineralization Mechanism from Recessive Osteogenesis Imperfecta

  David R. Eyre;Mary Ann Weis

  175
  Citations

• Mutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypes

  Shawna M. Pyott;Ulrike Schwarze;Helena E. Christiansen;Melanie G. Pepin

  166
  Citations

• Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen

  Ulrike Schwarze;Tim Cundy;Shawna M. Pyott;Helena E. Christiansen

  164
  Citations

• Abnormal Type I Collagen Post-translational Modification and Crosslinking in a Cyclophilin B KO Mouse Model of Recessive Osteogenesis Imperfecta

  Wayne A. Cabral;Irina Perdivara;MaryAnn A. Weis;Masahiko Terajima

  143
  Citations

• Recent developments in cartilage research: matrix biology of the collagen II/IX/XI heterofibril network.

  D. R. Eyre;J.-J. Wu;R. J. Fernandes;T. A. Pietka

  139
  Citations