Marc F Hansen

Summary

Affiliation: University of Connecticut Health Center
Country: USA

Publications

  1. ncbi request reprint Osteosarcoma in Paget's disease of bone
    Marc F Hansen
    Center for Molecular Medicine, University of Connecticut Health Center, Farmington, Connecticut 06030, USA
    J Bone Miner Res 21:P58-63. 2006
  2. pmc Somatic mutations in SQSTM1 detected in affected tissues from patients with sporadic Paget's disease of bone
    Anand Merchant
    Center for Molecular Medicine, University of Connecticut Health Center, Farmington, Connecticut 06030, USA
    J Bone Miner Res 24:484-94. 2009
  3. ncbi request reprint Expression of receptor activator of nuclear factor-kappaB is inversely correlated with metastatic phenotype in breast carcinoma
    Pardeep Bhatia
    Center for Molecular Medicine, University of Connecticut Health Center, Farmington, Connecticut 06030, USA
    Clin Cancer Res 11:162-5. 2005
  4. ncbi request reprint Determination of a minimal region of loss of heterozygosity on chromosome 18q21.33 in osteosarcoma
    Teresa L Johnson-Pais
    Department of Pediatrics, University of Texas Health Science Center, San Antonio, TX, USA
    Int J Cancer 105:285-8. 2003
  5. ncbi request reprint Analysis of environmental factors in familial versus sporadic Paget's disease of bone--the New England Registry for Paget's Disease of Bone
    Margaret Seton
    Arthritis Unit, New England Registry for Paget s Disease of Bone, Massachusetts General Hospital, Boston, Massachusetts 02114, USA
    J Bone Miner Res 18:1519-24. 2003
  6. ncbi request reprint Three novel mutations in SQSTM1 identified in familial Paget's disease of bone
    Teresa L Johnson-Pais
    Department of Pediatrics, University of Texas Health Science Center, San Antonio, Texas 78229, USA
    J Bone Miner Res 18:1748-53. 2003

Collaborators

  • Teresa L Johnson-Pais
  • Margaret Seton
  • Robin J Leach
  • Pardeep Bhatia
  • Anand Merchant
  • Elizabeth A Saria
  • John D Delaney
  • Magda Smielewska
  • Nimit Patel
  • Jennifer D Akunowicz
  • M Melinda Sanders
  • Julie H Wisdom
  • Hyon K Choi
  • Frederick R Singer
  • Dharmini Pathmanathan
  • Donald G Ammerman
  • Jannine D Cody
  • Carolyn L Buller
  • Korri S Weldon
  • Maggie J Nellissery
  • Rolf J Sebaldt
  • Cyrus Cooper

Detail Information

Publications6

  1. ncbi request reprint Osteosarcoma in Paget's disease of bone
    Marc F Hansen
    Center for Molecular Medicine, University of Connecticut Health Center, Farmington, Connecticut 06030, USA
    J Bone Miner Res 21:P58-63. 2006
    ....
  2. pmc Somatic mutations in SQSTM1 detected in affected tissues from patients with sporadic Paget's disease of bone
    Anand Merchant
    Center for Molecular Medicine, University of Connecticut Health Center, Farmington, Connecticut 06030, USA
    J Bone Miner Res 24:484-94. 2009
    ..The discovery of somatically acquired mutations in both the diseased bone and tumor samples suggests a paradigm shift in our understanding of this disease...
  3. ncbi request reprint Expression of receptor activator of nuclear factor-kappaB is inversely correlated with metastatic phenotype in breast carcinoma
    Pardeep Bhatia
    Center for Molecular Medicine, University of Connecticut Health Center, Farmington, Connecticut 06030, USA
    Clin Cancer Res 11:162-5. 2005
    ..Stimulation of the normal osteoblasts and stromal cells by the tumor cells may then lead to secondary osteoclastogenesis, resulting in the osteolytic phenotype common to breast metastases...
  4. ncbi request reprint Determination of a minimal region of loss of heterozygosity on chromosome 18q21.33 in osteosarcoma
    Teresa L Johnson-Pais
    Department of Pediatrics, University of Texas Health Science Center, San Antonio, TX, USA
    Int J Cancer 105:285-8. 2003
    ..33. This new region is approximately 500 kb and contains at least 7 known genes; however, it excludes 2 previous candidate genes: TNFRSF11A (RANK) and BCL2...
  5. ncbi request reprint Analysis of environmental factors in familial versus sporadic Paget's disease of bone--the New England Registry for Paget's Disease of Bone
    Margaret Seton
    Arthritis Unit, New England Registry for Paget s Disease of Bone, Massachusetts General Hospital, Boston, Massachusetts 02114, USA
    J Bone Miner Res 18:1519-24. 2003
    ..Those with a family history of PD (20%) suffered earlier deformity and fracture, and tended to have grandparents born abroad. These findings suggest heritage is important in PD; the role of environment remains unclear...
  6. ncbi request reprint Three novel mutations in SQSTM1 identified in familial Paget's disease of bone
    Teresa L Johnson-Pais
    Department of Pediatrics, University of Texas Health Science Center, San Antonio, Texas 78229, USA
    J Bone Miner Res 18:1748-53. 2003
    ..Disruptions of the C-terminal domain of SQSTM1 seem to be a leading cause of familial PDB...