Search Results - "Baud'huin, M"

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    Sostdc1: A soluble BMP and Wnt antagonist that is induced by the interaction between myeloma cells and osteoblast lineage cells by Faraahi, Z., Baud'huin, M., Croucher, P.I., Eaton, C., Lawson, M.A.

    Published in Bone (New York, N.Y.) (01-05-2019)
    “…Multiple myeloma (MM) is characterised by destructive lytic bone disease, caused by induction of bone resorption and impaired bone formation. Our understanding…”
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    Risk factors for failure of pre-cut eye bank UT-DSAEK grafts by Bodénès, F, Eude, Y, Baud'huin, M, Vabres, B, Weber, M, Le Meur, G, Orignac, I

    Published in Journal francais d'ophtalmologie (01-04-2023)
    “…The main risk factors for graft failure in penetrating keratoplasty are well known. However, few studies have examined donor characteristics or more precise…”
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    Effects of a sulfated exopolysaccharide produced by Altermonas infernus on bone biology by Velasco, C Ruiz, Baud'huin, M, Sinquin, C, Maillasson, M, Heymann, D, Colliec-Jouault, S, Padrines, M

    Published in Glycobiology (Oxford) (01-06-2011)
    “…The growth and differentiation of bone cells is controlled by various factors, which can be modulated by heparan sulfates. Here, we investigated the effects of…”
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    Key roles of the OPG-RANK-RANKL system in bone oncology by Baud huin, M, Duplomb, L, Velasco, C Ruiz, Fortun, Y, Heymann, D, Padrines, M

    Published in Expert review of anticancer therapy (01-02-2007)
    “…Osteoprotegerin (OPG)-receptor activator of nuclear factor- B (RANK) and RANK ligand (RANKL) have been identified as members of a ligand-receptor system that…”
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    Confirming Variants in Next-Generation Sequencing Panel Testing by Sanger Sequencing by Baudhuin, Linnea M, Lagerstedt, Susan A, Klee, Eric W, Fadra, Numrah, Oglesbee, Devin, Ferber, Matthew J

    Published in The Journal of molecular diagnostics : JMD (01-07-2015)
    “…Current clinical laboratory practice guidelines for next-generation sequencing (NGS) do not provide definitive guidance on confirming NGS variants. Sanger…”
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    Decreased frequency of FBN1 missense variants in Ghent criteria-positive Marfan syndrome and characterization of novel FBN1 variants by Baudhuin, Linnea M, Kotzer, Katrina E, Lagerstedt, Susan A

    Published in Journal of human genetics (01-05-2015)
    “…The diagnosis of Marfan syndrome (MFS) remains challenging despite the 2010 revision to Ghent nosology criteria, and there is a lack of published information…”
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    IL-33 is expressed in human osteoblasts, but has no direct effect on bone remodeling by Saidi, S., Bouri, F., Lencel, P., Duplomb, L., Baud’huin, M., Delplace, S., Leterme, D., Miellot, F., Heymann, D., Hardouin, P., Palmer, G., Magne, D.

    Published in Cytokine (Philadelphia, Pa.) (01-03-2011)
    “…The aim of the present study was to investigate the potential role of the recently discovered IL-1 family member IL-33 in bone remodeling. Our results indicate…”
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    UGT1A1 Genetic Analysis as a Diagnostic Aid for Individuals with Unconjugated Hyperbilirubinemia by Skierka, Jennifer M., BS, Kotzer, Katrina E., MS, Lagerstedt, Susan A., BS, O'Kane, Dennis J., PhD, Baudhuin, Linnea M., PhD

    Published in The Journal of pediatrics (01-06-2013)
    “…Objective To assess the clinical utility of UGT1A1 genetic testing and describe the spectrum and prevalence of UGT1A1 variations identified in pediatric…”
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    What Is the True Prevalence of Hypertrophic Cardiomyopathy? by Baudhuin, Linnea M., PhD, Kotzer, Katrina E., MS, CGC, Kluge, Michelle L., MS, CGC, Maleszewski, Joseph J., MD

    “…Technological advances have allowed us to more comprehensively and efficiently interrogate human genomes, and there are a number of large-scale efforts, such…”
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    Prevalence and Spectrum of Large Deletions or Duplications in the Major Long QT Syndrome-Susceptibility Genes and Implications for Long QT Syndrome Genetic Testing by Tester, David J., BS, Benton, Amber J., BS, Train, Laura, BS, Deal, Barbara, MD, Baudhuin, Linnea M., PhD, Ackerman, Michael J., MD, PhD

    Published in The American journal of cardiology (15-10-2010)
    “…Long QT syndrome (LQTS) is a cardiac channelopathy associated with syncope, seizures, and sudden death. Approximately 75% of LQTS is due to mutations in genes…”
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    Determination of the Duplicated CYP2D6 Allele Using Real-Time PCR Signal: An Alternative Approach by Atiq, Mazen A, Peterson, Sandra E, Langman, Loralie J, Baudhuin, Linnea M, Black, John L, Moyer, Ann M

    Published in Journal of personalized medicine (24-05-2023)
    “…duplication has important pharmacogenomic implications. Reflex testing with long-range PCR (LR-PCR) can resolve the genotype when a duplication and alleles…”
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    Sphingosylphosphorylcholine and Lysophosphatidylcholine Are Ligands for the G Protein-coupled Receptor GPR4 by Zhu, Kui, Baudhuin, Linnea M., Hong, Guiying, Williams, Freager S., Cristina, Kelly L., Kabarowski, Janusz H.S., Witte, Owen N., Xu, Yan

    Published in The Journal of biological chemistry (02-11-2001)
    “…Sphingosylphosphorylcholine (SPC) and lysophosphatidylcholine (LPC) are bioactive lipid molecules involved in numerous biological processes. We have recently…”
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    RANKL, RANK, osteoprotegerin: key partners of osteoimmunology and vascular diseases by Baud'huin, M, Lamoureux, F, Duplomb, L, Rédini, F, Heymann, D

    “…1997 saw the identification of a novel set of proteins within the tumor necrosis factor (TNF)/TNF receptor families that are required for the control of bone…”
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