Search Results - "Murray, J. C."

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  1. 1

    Global burden of depressive disorders in the year 2000 by Üstün, T. B., Ayuso-Mateos, J. L., Chatterji, S., Mathers, C., Murray, C. J. L.

    Published in British journal of psychiatry (01-05-2004)
    “…The initial Global Burden of Disease study found that depression was the fourth leading cause of disease burden, accounting for 3.7% of total disability…”
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    Journal Article
  2. 2

    Gene/environment causes of cleft lip and/or palate by Murray, JC

    Published in Clinical genetics (01-04-2002)
    “…Craniofacial anomalies, and in particular cleft lip and palate, are major human birth defects with a worldwide frequency of 1 in 700 and substantial clinical…”
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    Journal Article
  3. 3

    Folic acid and orofacial clefts: a review of the evidence by Wehby, GL, Murray, JC

    Published in Oral diseases (01-01-2010)
    “…Orofacial clefts are common and burdensome birth defects with a complex genetic and environmental etiology. The contribution of nutritional factors and…”
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    Journal Article
  4. 4

    PI(3) kinase is associated with a mechanism of immunoresistance in breast and prostate cancer by Crane, C A, Panner, A, Murray, J C, Wilson, S P, Xu, H, Chen, L, Simko, J P, Waldman, F M, Pieper, R O, Parsa, A T

    Published in Oncogene (15-01-2009)
    “…Immune escape describes a critical event whereby tumor cells adopt an immunoresistant phenotype to escape adaptive surveillance. We show that expression of a…”
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    Journal Article
  5. 5

    Evaluating rare coding variants as contributing causes to non-syndromic cleft lip and palate by Leslie, EJ, Murray, JC

    Published in Clinical genetics (01-11-2013)
    “…Rare coding variants are a current focus in studies of complex disease. Previously, at least 68 rare coding variants were reported from candidate gene…”
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    Journal Article
  6. 6

    A framework for assessing the performance of health systems: Health Systems by MURRAY, C. J. L, FRENK, J

    Published in Bulletin of the World Health Organization (01-06-2000)
    “…Health systems vary widely in performance, and countries with similar levels of income, education and health expenditure differ in their ability to attain key…”
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    Journal Article
  7. 7

    Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study by Beaty, T. H., Taub, M. A., Scott, A. F., Murray, J. C., Marazita, M. L., Schwender, H., Parker, M. M., Hetmanski, J. B., Balakrishnan, P., Mansilla, M. A., Mangold, E., Ludwig, K. U., Noethen, M. M., Rubini, M., Elcioglu, N., Ruczinski, I.

    Published in Human genetics (01-07-2013)
    “…A collection of 1,108 case–parent trios ascertained through an isolated, nonsyndromic cleft lip with or without cleft palate (CL/P) was used to replicate the…”
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    Journal Article
  8. 8

    Clinical findings in patients with GLI2 mutations - phenotypic variability by Bertolacini, CDP, Ribeiro-Bicudo, LA, Petrin, A, Richieri-Costa, A, Murray, JC

    Published in Clinical genetics (01-01-2012)
    “…Bertolacini CDP, Ribeiro‐Bicudo LA, Petrin A, Richieri‐Costa A, Murray JC. Clinical findings in patients with GLI2 mutations – phenotypic variability…”
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    Journal Article
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    Peptide Templates for Nanoparticle Synthesis Derived from Polymerase Chain Reaction-Driven Phage Display by Naik, R. R., Jones, S. E., Murray, C. J., McAuliffe, J. C., Vaia, R. A., Stone, M. O.

    Published in Advanced functional materials (01-01-2004)
    “…Phage peptide display libraries are commonly used to select peptides that bind to inorganic surfaces (metals, metal oxides, and semiconductors). These binding…”
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    Journal Article
  11. 11

    MSX1, PAX9, and TGFA Contribute to Tooth Agenesis in Humans by Vieira, A.R., Meira, R., Modesto, A., Murray, J.C.

    Published in Journal of dental research (01-09-2004)
    “…In this study, we sought to determine the association between tooth agenesis and DNA sequence variation in the genes MSX1 and PAX9 in an ethnically diverse…”
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    Journal Article
  12. 12

    Armed conflict as a public health problem by Murray, C J L, King, G, Lopez, A D, Tomijima, N, Krug, E G

    Published in BMJ (09-02-2002)
    “…Given the necessary caveats about the accuracy of epidemiological assessment table 2 puts the potential size of mortality directly related to conflict in…”
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    Journal Article
  13. 13

    Synthetic lethal screening reveals FGFR as one of the combinatorial targets to overcome resistance to Met-targeted therapy by Kim, B, Wang, S, Lee, J M, Jeong, Y, Ahn, T, Son, D-S, Park, H W, Yoo, H-s, Song, Y-J, Lee, E, Oh, Y M, Lee, S B, Choi, J, Murray, J C, Zhou, Y, Song, P H, Kim, K-A, Weiner, L M

    Published in Oncogene (26-02-2015)
    “…Met is a receptor tyrosine kinase that promotes cancer progression. In addition, Met has been implicated in resistance of tumors to various targeted therapies…”
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    A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palate by Abidi, FE, Miano, MG, Murray, JC, Schwartz, CE

    Published in Clinical genetics (01-07-2007)
    “…Recently, two truncating mutations in the PHF8 (plant homeodomain finger protein 8) gene have been found to cause X‐linked mental retardation associated with…”
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    Journal Article
  16. 16

    DNA methylation differences in monozygotic twins with Van der Woude syndrome by Petrin, A L, Zeng, E, Thomas, M A, Moretti-Ferreira, D, Marazita, M L, Xie, X J, Murray, J C, Moreno-Uribe, L M

    Published in Frontiers in dental medicine (2023)
    “…Van der Woude Syndrome (VWS) is an autosomal dominant disorder responsible for 2% of all syndromic orofacial clefts (OFCs) with being the primary causal gene…”
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    Journal Article
  17. 17

    Global Burden of Untreated Caries: A Systematic Review and Metaregression by Kassebaum, N.J., Bernabé, E., Dahiya, M., Bhandari, B., Murray, C.J.L., Marcenes, W.

    Published in Journal of Dental Research (01-05-2015)
    “…We aimed to consolidate all epidemiologic data about untreated caries and subsequently generate internally consistent prevalence and incidence estimates for…”
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    Book Review Journal Article
  18. 18

    Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate by Jezewski, P A, Vieira, A R, Nishimura, C, Ludwig, B, Johnson, M, O’Brien, S E, Daack-Hirsch, S, Schultz, R E, Weber, A, Nepomucena, B, Romitti, P A, Christensen, K, Orioli, I M, Castilla, E E, Machida, J, Natsume, N, Murray, J C

    Published in Journal of medical genetics (01-06-2003)
    “…MSX1 has been proposed as a gene in which mutations may contribute to non-syndromic forms of cleft lip and/or cleft palate. Support for this comes from human…”
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    Journal Article
  19. 19

    Quantifying the burden of disease: the technical basis for disability-adjusted life years by MURRAY, C. J. L

    Published in Bulletin of the World Health Organization (01-05-1994)
    “…Detailed assumptions used in constructing a new indicator of the burden of disease, the disability-adjusted life year (DALY), are presented. Four key social…”
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    Journal Article
  20. 20

    Measuring Quality of Health Care from the User's Perspective in 41 Countries: Psychometric Properties of WHO's Questions on Health Systems Responsiveness by Valentine, N. B., Bonsel, G. J., Murray, C. J. L.

    Published in Quality of life research (01-09-2007)
    “…Objective To evaluate, for different populations, psychometric properties of questions on "health systems responsiveness", a concept developed by World Health…”
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    Journal Article