These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

190 related items for PubMed ID: 9824535

  • 1. Using genetically engineered mice to understand apolipoprotein-B deficiency syndromes in humans.
    Raabe M, Kim E, Véniant M, Nielsen LB, Young SG.
    Proc Assoc Am Physicians; 1998; 110(6):521-30. PubMed ID: 9824535
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Anderson's disease: genetic exclusion of the apolipoprotein-B gene in two families.
    Pessah M, Benlian P, Beucler I, Loux N, Schmitz J, Junien C, Infante R.
    J Clin Invest; 1991 Jan; 87(1):367-70. PubMed ID: 1985110
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins.
    Young SG, Hubl ST, Smith RS, Snyder SM, Terdiman JF.
    J Clin Invest; 1990 Mar; 85(3):933-42. PubMed ID: 2312735
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. The hypobetalipoproteinemias.
    Schonfeld G.
    Annu Rev Nutr; 1995 Mar; 15():23-34. PubMed ID: 8527219
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. 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.
    Kim E, Cham CM, Véniant MM, Ambroziak P, Young SG.
    J Clin Invest; 1998 Mar 15; 101(6):1468-77. PubMed ID: 9502790
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Anderson's disease: exclusion of apolipoprotein and intracellular lipid transport genes.
    Dannoura AH, Berriot-Varoqueaux N, Amati P, Abadie V, Verthier N, Schmitz J, Wetterau JR, Samson-Bouma ME, Aggerbeck LP.
    Arterioscler Thromb Vasc Biol; 1999 Oct 15; 19(10):2494-508. PubMed ID: 10521380
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. The role of the microsomal triglygeride transfer protein in abetalipoproteinemia.
    Berriot-Varoqueaux N, Aggerbeck LP, Samson-Bouma M, Wetterau JR.
    Annu Rev Nutr; 2000 Oct 15; 20():663-97. PubMed ID: 10940349
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.