Search Results - "Raggio, C L"

  • Showing 1 - 19 results of 19
Refine Results
  1. 1

    Clinical, Genetic and Environmental Factors Associated with Congenital Vertebral Malformations by Giampietro, P.F., Raggio, C.L., Blank, R.D., McCarty, C., Broeckel, U., Pickart, M.A.

    Published in Molecular syndromology (01-02-2013)
    “…Congenital vertebral malformations (CVM) pose a significant health problem because they can be associated with spinal deformities, such as congenital scoliosis…”
    Get full text
    Journal Article
  2. 2

    An analysis of PAX1 in the development of vertebral malformations by Giampietro, PF, Raggio, CL, Reynolds, CE, Shukla, SK, McPherson, E, Ghebranious, N, Jacobsen, FS, Kumar, V, Faciszewski, T, Pauli, RM, Rasmussen, K, Burmester, JK, Zaleski, C, Merchant, S, David, D, Weber, JL, Glurich, I, Blank, RD

    Published in Clinical genetics (01-11-2005)
    “…Due to the sporadic occurrence of congenital vertebral malformations, traditional linkage approaches to identify genes associated with human vertebral…”
    Get full text
    Journal Article
  3. 3

    Fourier transform infrared imaging spectroscopy (FT-IRIS) of mineralization in bisphosphonate-treated oim/oim mice by Camacho, N P, Carroll, P, Raggio, C L

    Published in Calcified tissue international (01-05-2003)
    “…Fourier transform infrared microscopy (FT-IRM) and imaging spectroscopy (FT-IRIS) are increasingly used to analyze the molecular components of mineralized…”
    Get full text
    Journal Article
  4. 4

    The Material Basis for Reduced Mechanical Properties in oim Mice Bones by Camacho, Nancy P., Hou, Lindy, Toledano, Talya R., Ilg, W. Alex, Brayton, Cory F., Raggio, Cathleen L., Root, Leon, Boskey, Adele L.

    Published in Journal of bone and mineral research (01-02-1999)
    “…Osteogenesis imperfecta (OI), a heritable disease caused by molecular defects in type I collagen, is characterized by skeletal deformities and brittle bones…”
    Get full text
    Journal Article
  5. 5

    A controlled study of the effects of alendronate in a growing mouse model of osteogenesis imperfecta by Camacho, N P, Raggio, C L, Doty, S B, Root, L, Zraick, V, Ilg, W A, Toledano, T R, Boskey, A L

    Published in Calcified tissue international (01-08-2001)
    “…Recent studies have reported that bisphosphonates reduce fracture incidence and improve bone density in children with osteogenesis imperfecta (OI). However,…”
    Get full text
    Journal Article
  6. 6

    Congenital and Idiopathic Scoliosis: Clinical and Genetic Aspects by Giampietro, Philip F, Blank, Robert D, Raggio, Cathleen L, Merchant, Sajid, Jacobsen, F Stig, Faciszewski, Thomas, Shukla, Sanjay K, Greenlee, Anne R, Reynolds, Cory, Schowalter, David B

    Published in Clinical medicine & research (01-04-2003)
    “…Genetic and environmental factors influencing spinal development in lower vertebrates are likely to play a role in the abnormalities associated with human…”
    Get full text
    Journal Article
  7. 7

    A genomic approach to scoliosis pathogenesis by Blank, R D, Raggio, C L, Giampietro, P F, Camacho, N P

    Published in Lupus (01-01-1999)
    “…Genetic predisposition contributes to scoliosis in humans. Two syndromes of primary scoliosis occur — congenital scoliosis, which presents at birth, often…”
    Get full text
    Journal Article
  8. 8

    Identification of the oim mutation by dye terminator chemistry combined with automated direct DNA sequencing by Camacho, N P, Dow, D, Toledano, T R, Buckmeyer, J K, Gertner, J M, Brayton, C F, Raggio, C L, Root, L, Boskey, A L

    Published in Journal of orthopaedic research (01-01-1998)
    “…The homozygous oim/oim mouse, a model of moderate-to-severe human osteogenesis imperfecta, contains a G-nucleotide deletion in the Cola-2 gene (the murine pro…”
    Get more information
    Journal Article
  9. 9

    Synteny-defined candidate genes for congenital and idiopathic scoliosis by Giampietro, Philip F., Raggio, Cathleen L., Blank, Robert D.

    Published in American journal of medical genetics (19-03-1999)
    “…Idiopathic scoliosis (IS) is a common but poorly understood syndrome. Congenital scoliosis (CS) is less common but comparably unexplored. Previous studies…”
    Get full text
    Journal Article
  10. 10

    In vivo hydroxyapatite formation induced by lipids by Raggio, C.L., Boyan, B.D., Boskey, Adele L.

    Published in Journal of bone and mineral research (01-10-1986)
    “…Proteolipids and complexed acidic phospholipids that cause in vitro hydroxyapatite formation, similarly cause hydroxyapatite deposition in 10‐μ pore Millipore…”
    Get full text
    Journal Article
  11. 11
  12. 12

    Changes in the bone tissue lipids in persons with steroid- and alcohol-induced osteonecrosis by Boskey, A L, Raggio, C L, Bullough, P G, Kinnett, J G

    Published in Clinical orthopaedics and related research (01-01-1983)
    “…The lipids associated with osteonecrotic bone have a higher cholesterol content than those associated with normal (nondiseased) or osteoarthritic bone. A study…”
    Get more information
    Journal Article
  13. 13
  14. 14
  15. 15

    Osteogenesis imperfecta: potential therapeutic approaches by Rousseau, Maxime, Retrouvey, Jean-Marc

    Published in PeerJ (San Francisco, CA) (17-08-2018)
    “…Osteogenesis imperfecta (OI) is a genetic disorder that is usually caused by disturbed production of collagen type I. Depending on its severity in the patient,…”
    Get full text
    Journal Article
  16. 16
  17. 17
  18. 18

    Differential effects of alendronate treatment on bone from growing osteogenesis imperfecta and wild-type mouse by Misof, Barbara M., Roschger, Paul, Baldini, Todd, Raggio, Cathleen L., Zraick, Vivien, Root, Leon, Boskey, Adele L., Klaushofer, Klaus, Fratzl, Peter, Camacho, Nancy P.

    Published in Bone (New York, N.Y.) (01-01-2005)
    “…Bisphosphonates have been reported to decrease the number of fractures in children with osteogenesis imperfecta (OI). The current study sought to further…”
    Get full text
    Journal Article
  19. 19

    Short Report: An analysis of PAX1 in the development of vertebral malformations by Giampietro, P F, Raggio, CL, Reynolds, CE, Shukla, S K, McPherson, E, Ghebranious, N, Jacobsen, F S, Kumar, V, Faciszewski, T, Pauli, R M, Rasmussen, K, Burmester, J K, Zaleski, C, Merchant, S, David, D, Weber, J L, Glurich, I, Blank, R D

    Published in Clinical genetics (01-11-2005)
    “…Due to the sporadic occurrence of congenital vertebral malformations, traditional linkage approaches to identify genes associated with human vertebral…”
    Get full text
    Journal Article