Search Results - "Ambroziak, P"

  • Showing 1 - 19 results of 19
Refine Results
  1. 1
  2. 2
  3. 3

    Management of factor VII-deficient patients undergoing joint surgeries - preliminary results of locally developed treatment regimen by Windyga, J., Zbikowski, P., Ambroziak, P., Baran, B., Kotela, I., Stefanska-Windyga, E.

    “…Summary Inherited factor VII (FVII) deficiency is a rare coagulation disorder with variable haemorrhagic manifestations. In severely affected cases spontaneous…”
    Get full text
    Journal Article
  4. 4

    Absence of the CAAX Endoprotease Rce1: Effects on Cell Growth and Transformation by Bergo, Martin O., Ambroziak, Patricia, Gregory, Cria, George, Amanda, Otto, James C., Kim, Edward, Nagase, Hiroki, Casey, Patrick J., Balmain, Allan, Young, Stephen G.

    Published in Molecular and Cellular Biology (01-01-2002)
    “…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
    Get full text
    Journal Article
  5. 5

    Defining the atherogenicity of large and small lipoproteins containing apolipoprotein B100 by Véniant, M M, Sullivan, M A, Kim, S K, Ambroziak, P, Chu, A, Wilson, M D, Hellerstein, M K, Rudel, L L, Walzem, R L, Young, S G

    Published in The Journal of clinical investigation (15-12-2000)
    “…Apo-E-deficient apo-B100-only mice (APOE:(-/-)APOB:(100/100)) and LDL receptor-deficient apo-B100-only mice (LDLR:(-/-)APOB:(100/100)) have similar total…”
    Get full text
    Journal Article
  6. 6

    Targeted Inactivation of the Isoprenylcysteine Carboxyl Methyltransferase Gene Causes Mislocalization of K-Ras in Mammalian Cells by Bergo, Martin O., Leung, Gordon K., Ambroziak, Patricia, Otto, James C., Casey, Patrick J., Young, Stephen G.

    Published in The Journal of biological chemistry (09-06-2000)
    “…After isoprenylation and endoproteolytic processing, the Ras proteins are methylated at the carboxyl-terminal isoprenylcysteine. The importance of…”
    Get full text
    Journal Article
  7. 7

    Disruption of the Mouse Rce1 Gene Results in Defective Ras Processing and Mislocalization of Ras within Cells by Kim, E, Ambroziak, P, Otto, J C, Taylor, B, Ashby, M, Shannon, K, Casey, P J, Young, S G

    Published in The Journal of biological chemistry (26-03-1999)
    “…Little is known about the enzyme(s) required for the endoproteolytic processing of mammalian Ras proteins. We identified a mouse gene (designated Rce1 ) that…”
    Get full text
    Journal Article
  8. 8

    On the physiological importance of endoproteolysis of CAAX proteins: heart-specific RCE1 knockout mice develop a lethal cardiomyopathy by Bergo, Martin O, Lieu, Hsiao D, Gavino, Bryant J, Ambroziak, Patricia, Otto, James C, Casey, Patrick J, Walker, Quinn M, Young, Stephen G

    Published in The Journal of biological chemistry (06-02-2004)
    “…Proteins terminating with a CAAX motif, such as the Ras proteins and the nuclear lamins, undergo post-translational modification of a C-terminal cysteine with…”
    Get full text
    Journal Article
  9. 9
  10. 10
  11. 11
  12. 12

    Isoprenylcysteine Carboxyl Methyltransferase Deficiency in Mice by Bergo, Martin O., Leung, Gordon K., Ambroziak, Patricia, Otto, James C., Casey, Patrick J., Gomes, Anita Q., Seabra, Miguel C., Young, Stephen G.

    Published in The Journal of biological chemistry (23-02-2001)
    “…After isoprenylation, Ras and other CAAX proteins undergo endoproteolytic processing by Rce1 and methylation of the isoprenylcysteine by Icmt…”
    Get full text
    Journal Article
  13. 13

    Dual mechanisms for the low plasma levels of truncated apolipoprotein B proteins in familial hypobetalipoproteinemia. Analysis of a new mouse model with a nonsense mutation in the Apob gene by Kim, E, Cham, C M, Véniant, M M, Ambroziak, P, Young, S G

    Published in The Journal of clinical investigation (15-03-1998)
    “…Familial hypobetalipoproteinemia (FHbeta), a syndrome characterized by low plasma cholesterol levels, is caused by mutations in the apo-B gene that interfere…”
    Get full text
    Journal Article
  14. 14

    A gene-targeted mouse model for familial hypobetalipoproteinemia. Low levels of apolipoprotein B mRNA in association with a nonsense mutation in exon 26 of the apolipoprotein B gene by Kim, E. (University of California, San Francisco, CA.), Ambroziak, P, Veniant, M.M, Hamilton, R.L, Young, S.G

    Published in The Journal of biological chemistry (18-12-1998)
    “…Familial hypobetalipoproteinemia, a syndrome characterized by abnormally low plasma levels of low density lipoprotein cholesterol, is caused by mutations in…”
    Get full text
    Journal Article
  15. 15

    Generation of monoclonal antibodies specific for mouse apolipoprotein B-100 in apolipoprotein B-48-only mice by Zlot, C H, Flynn, L M, Véniant, M M, Kim, E, Raabe, M, McCormick, S P, Ambroziak, P, McEvoy, L M, Young, S G

    Published in Journal of lipid research (01-01-1999)
    “…Over the past 10 years, many laboratories have investigated lipid metabolism and atherogenesis with a variety of transgenic and gene knockout mouse models…”
    Get full text
    Journal Article
  16. 16
  17. 17
  18. 18
  19. 19