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

Journal Abstract Search


247 related items for PubMed ID: 18166993

  • 21. HEMPAS disease: genetic defect of glycosylation.
    Fukuda MN.
    Glycobiology; 1990 Sep; 1(1):9-15. PubMed ID: 2136385
    [Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23. Plasma N-glycan profiling by mass spectrometry for congenital disorders of glycosylation type II.
    Guillard M, Morava E, van Delft FL, Hague R, Körner C, Adamowicz M, Wevers RA, Lefeber DJ.
    Clin Chem; 2011 Apr; 57(4):593-602. PubMed ID: 21273509
    [Abstract] [Full Text] [Related]

  • 24. High-mannose-type oligosaccharides from human placental arylsulfatase A are core fucosylated as confirmed by MALDI MS.
    Hoja-Lukowicz D, Ciołczyk D, Bergquist J, Lityńska A, Laidler P.
    Glycobiology; 2000 Jun; 10(6):551-7. PubMed ID: 10814696
    [Abstract] [Full Text] [Related]

  • 25. Decreased glycosylation of band 3 and band 4.5 glycoproteins of erythrocyte membrane in congenital dyserythropoietic anaemia type II.
    Scartezzini P, Forni GL, Baldi M, Izzo C, Sansone G.
    Br J Haematol; 1982 Aug; 51(4):569-76. PubMed ID: 7104237
    [Abstract] [Full Text] [Related]

  • 26. [Abnormalities of the erythrocyte membrane ultrastructure and the membrane proteins in a patient with HEMPAS, alpha thalassemia and complicated diabetes].
    Li JY, Xu YQ, Huang ZX, Zhou H, Wan SD.
    Zhonghua Nei Ke Za Zhi; 2004 Jun; 43(6):426-8. PubMed ID: 15312436
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. [Diagnosis and genetics of congenital dyserythropoietic anemias (CDA)].
    Rössler J, Havers W.
    Klin Padiatr; 2000 Jun; 212(4):153-8. PubMed ID: 10994542
    [Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Ineffective erythropoiesis underlies the clinical heterogeneity of congenital dyserythropoietic anemia type II (CDA II).
    Kostaridou S, Polychronopoulou S, Premetis E, Papassotiriou I, Stamoulakatou A, Haidas S.
    Pediatr Int; 2004 Jun; 46(3):274-9. PubMed ID: 15151542
    [Abstract] [Full Text] [Related]

  • 33. Chemical and enzymatic N-glycan release comparison for N-glycan profiling of monoclonal antibodies expressed in plants.
    Triguero A, Cabrera G, Royle L, Harvey DJ, Rudd PM, Dwek RA, Bardor M, Lerouge P, Cremata JA.
    Anal Biochem; 2010 May 15; 400(2):173-83. PubMed ID: 20109437
    [Abstract] [Full Text] [Related]

  • 34. Congenital disorders of glycosylation type I leads to altered processing of N-linked glycans, as well as underglycosylation.
    Mills P, Mills K, Clayton P, Johnson A, Whitehouse D, Winchester B.
    Biochem J; 2001 Oct 15; 359(Pt 2):249-54. PubMed ID: 11583570
    [Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. Characterization of N-glycosylations in Entamoeba histolytica ubiquitin.
    Obregón A, Flores MS, Rangel R, Arévalo K, Maldonado G, Quintero I, Galán L.
    Exp Parasitol; 2019 Jan 15; 196():38-47. PubMed ID: 30444974
    [Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Enzymatic deglycosylation of human Band 3, the anion transport protein of the erythrocyte membrane. Effect on protein structure and transport properties.
    Casey JR, Pirraglia CA, Reithmeier RA.
    J Biol Chem; 1992 Jun 15; 267(17):11940-8. PubMed ID: 1601863
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 13.