William M Maniscalco

Summary

Affiliation: University of Rochester
Country: USA

Publications

  1. ncbi Angiogenic factors and alveolar vasculature: development and alterations by injury in very premature baboons
    William M Maniscalco
    Division of Neonatology, Strong Children s Research Center, Department of Pediatrics, University of Rochester, 601 Elmwood Ave, Rochester, NY 14642, USA
    Am J Physiol Lung Cell Mol Physiol 282:L811-23. 2002
  2. ncbi Hyperoxic ventilated premature baboons have increased p53, oxidant DNA damage and decreased VEGF expression
    William M Maniscalco
    Division of Neonatology, Children s Research Center, Pulmonary Biology and Disease Program, University of Rochester School of Medicine, Rochester, NY 14642, USA
    Pediatr Res 58:549-56. 2005
  3. ncbi Increased epithelial cell proliferation in very premature baboons with chronic lung disease
    William M Maniscalco
    Division of Neonatology, Strong Children s Research Center, Department of Pediatrics, University of Rochester, Rochester, New York 14642, USA
    Am J Physiol Lung Cell Mol Physiol 283:L991-L1001. 2002
  4. ncbi Type II epithelial cells are critical target for hyperoxia-mediated impairment of postnatal lung development
    Min Yee
    Department of Pediatrics, Box 850, University of Rochester, School of Medicine and Dentistry, 601 Elmwood Ave, NY 14642, USA
    Am J Physiol Lung Cell Mol Physiol 291:L1101-11. 2006
  5. ncbi Pathogenesis of bronchopulmonary dysplasia
    Patricia R Chess
    Department of Pediatrics, University of Rochester, Rochester, NY 14642, USA
    Semin Perinatol 30:171-8. 2006
  6. ncbi Murine mechanical ventilation stimulates alveolar epithelial cell proliferation
    Patricia Rose Chess
    Departments of Pediatrics and Biomedical Engineering, University of Rochester, Rochester, New York 14642, USA patricia
    Exp Lung Res 36:331-41. 2010
  7. ncbi Induced p21Cip1 in premature baboons with CLD: implications for alveolar hypoplasia
    MICHAEL A O'REILLY
    Dept of Pediatrics, Box 850, Univ of Rochester, 601 Elm wood Ave, Rochester, NY 14642, USA
    Am J Physiol Lung Cell Mol Physiol 285:L964-71. 2003
  8. ncbi In vivo exposure to hyperoxia induces DNA damage in a population of alveolar type II epithelial cells
    Jason M Roper
    Dept. of Pediatrics, Box 850, School of Medicine and Dentistry, Univ. of Rochester, 601 Elmwood Ave, Rochester, NY 14642, USA
    Am J Physiol Lung Cell Mol Physiol 286:L1045-54. 2004
  9. ncbi Normal remodeling of the oxygen-injured lung requires the cyclin-dependent kinase inhibitor p21(Cip1/WAF1/Sdi1)
    Rhonda J Staversky
    Department of Pediatrics, School of Medicine and Dentistry, University of Rochester, Rochester, New York 14642, USA
    Am J Pathol 161:1383-93. 2002
  10. ncbi The role of vascular growth factors in hyperoxia-induced injury to the developing lung
    CARL T D'ANGIO
    Strong Children s Research Center, Department of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester NY, USA
    Front Biosci 7:d1609-23. 2002

Research Grants

  1. Regulation of Microvascular Development in BPD
    William Maniscalco; Fiscal Year: 2006

Collaborators

Detail Information

Publications12

  1. ncbi Angiogenic factors and alveolar vasculature: development and alterations by injury in very premature baboons
    William M Maniscalco
    Division of Neonatology, Strong Children s Research Center, Department of Pediatrics, University of Rochester, 601 Elmwood Ave, Rochester, NY 14642, USA
    Am J Physiol Lung Cell Mol Physiol 282:L811-23. 2002
    ..These data suggest that CLD impairs lung microvascular development and that a possible mechanism is disruption of VEGF and Flt-1 expression...
  2. ncbi Hyperoxic ventilated premature baboons have increased p53, oxidant DNA damage and decreased VEGF expression
    William M Maniscalco
    Division of Neonatology, Children s Research Center, Pulmonary Biology and Disease Program, University of Rochester School of Medicine, Rochester, NY 14642, USA
    Pediatr Res 58:549-56. 2005
    ..The findings suggest that oxidant DNA damage may be a mechanism of increased p53 in hyperoxic fetal lung...
  3. ncbi Increased epithelial cell proliferation in very premature baboons with chronic lung disease
    William M Maniscalco
    Division of Neonatology, Strong Children s Research Center, Department of Pediatrics, University of Rochester, Rochester, New York 14642, USA
    Am J Physiol Lung Cell Mol Physiol 283:L991-L1001. 2002
    ..These data show that the development of chronic lung disease is associated with major alterations in normal patterns of lung-cell proliferation...
  4. ncbi Type II epithelial cells are critical target for hyperoxia-mediated impairment of postnatal lung development
    Min Yee
    Department of Pediatrics, Box 850, University of Rochester, School of Medicine and Dentistry, 601 Elmwood Ave, NY 14642, USA
    Am J Physiol Lung Cell Mol Physiol 291:L1101-11. 2006
    ..These data suggest that perinatal hyperoxia adversely affects alveolar development by disrupting the proper timing of type II cell proliferation and differentiation into type I cells...
  5. ncbi Pathogenesis of bronchopulmonary dysplasia
    Patricia R Chess
    Department of Pediatrics, University of Rochester, Rochester, NY 14642, USA
    Semin Perinatol 30:171-8. 2006
    ..The contribution of hyperoxia and hypoxia, mechanical forces, vascular maldevelopment, inflammation, fluid management, patent ductus arteriosus (PDA), nutrition, and genetics will be discussed...
  6. ncbi Murine mechanical ventilation stimulates alveolar epithelial cell proliferation
    Patricia Rose Chess
    Departments of Pediatrics and Biomedical Engineering, University of Rochester, Rochester, New York 14642, USA patricia
    Exp Lung Res 36:331-41. 2010
    ..Ventilation did not increase apoptosis in alveolar type II cells, as measured by TUNEL staining. Ventilation at low tidal volumes leads to a mild inflammatory response and alveolar epithelial cell proliferation...
  7. ncbi Induced p21Cip1 in premature baboons with CLD: implications for alveolar hypoplasia
    MICHAEL A O'REILLY
    Dept of Pediatrics, Box 850, Univ of Rochester, 601 Elm wood Ave, Rochester, NY 14642, USA
    Am J Physiol Lung Cell Mol Physiol 285:L964-71. 2003
    ..These data suggest that p21 may play a role in disorganized proliferation and alveolar hypoplasia seen in newborn chronic lung disease...
  8. ncbi In vivo exposure to hyperoxia induces DNA damage in a population of alveolar type II epithelial cells
    Jason M Roper
    Dept. of Pediatrics, Box 850, School of Medicine and Dentistry, Univ. of Rochester, 601 Elmwood Ave, Rochester, NY 14642, USA
    Am J Physiol Lung Cell Mol Physiol 286:L1045-54. 2004
    ..These data reveal that type II cells exposed to in vivo hyperoxia have oxidized and fragmented DNA. Because type II cells are essential for lung remodeling, our findings raise the possibility that they are proficient in DNA repair...
  9. ncbi Normal remodeling of the oxygen-injured lung requires the cyclin-dependent kinase inhibitor p21(Cip1/WAF1/Sdi1)
    Rhonda J Staversky
    Department of Pediatrics, School of Medicine and Dentistry, University of Rochester, Rochester, New York 14642, USA
    Am J Pathol 161:1383-93. 2002
    ..This observation has important implications for therapeutic strategies designed to attenuate long-term chronic lung disease after oxidant injury...
  10. ncbi The role of vascular growth factors in hyperoxia-induced injury to the developing lung
    CARL T D'ANGIO
    Strong Children s Research Center, Department of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester NY, USA
    Front Biosci 7:d1609-23. 2002
    ..Strategies that enhance microvascular integrity, whether through attenuating alterations in vascular growth factors or by other means, also improve the outcome of lung injury. Such therapies may eventually offer hope in human BPD...
  11. ncbi Bronchopulmonary dysplasia in preterm infants: pathophysiology and management strategies
    CARL T D'ANGIO
    Strong Children s Research Center, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA
    Paediatr Drugs 6:303-30. 2004
    ..Future research in BPD will most probably focus on continued incremental improvements in outcome, which are likely to be achieved through the combined effects of many therapeutic modalities...
  12. ncbi Survival in early- and late-term infants with congenital diaphragmatic hernia treated with extracorporeal membrane oxygenation
    Timothy P Stevens
    Division of Neonatology, Department of Pediatrics, Strong Children s Research Center, Golisano Children s Hospital at Strong, Rochester, New York 14642, USA
    Pediatrics 110:590-6. 2002
    ..Changes in survival rates of term infants and the factors associated with these changes were assessed over the 25 years that ECMO has been available...

Research Grants1

  1. Regulation of Microvascular Development in BPD
    William Maniscalco; Fiscal Year: 2006
    ..New data from this proposal will be essential for developing novel therapies for BPD. ..