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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 9242967)

  • 21. Phenotypic polymorphism of haptoglobin: a novel risk factor for the development of infection in liver cirrhosis.
    Vitalis Z; Altorjay I; Tornai I; Palatka K; Kacska S; Palyu E; Tornai D; Udvardy M; Harsfalvi J; Dinya T; Veres G; Lakatos PL; Papp M
    Hum Immunol; 2011 Apr; 72(4):348-54. PubMed ID: 21262313
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Haptoglobin: a review of the major allele frequencies worldwide and their association with diseases.
    Carter K; Worwood M
    Int J Lab Hematol; 2007 Apr; 29(2):92-110. PubMed ID: 17474882
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Novel haptoglobin insertion/deletion polymorphism is associated with the lipid profile and C-reactive protein (CRP) concentration.
    Wuyts B; Hetet G; Grandchamp B; Delanghe JR
    Clin Chem Lab Med; 2002 May; 40(5):469-74. PubMed ID: 12113290
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Haptoglobin polymorphism as a risk factor for chronic kidney disease: a case-control study.
    Chen YC; Lee CC; Huang CY; Huang HB; Yu CC; Ho YC; Su YC
    Am J Nephrol; 2011; 33(6):510-4. PubMed ID: 21546768
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Haptoglobin genotype and outcome after spontaneous intracerebral haemorrhage.
    Hostettler IC; Morton MJ; Ambler G; Kazmi N; Gaunt T; Wilson D; Shakeshaft C; Jäger HR; Cohen H; Yousry TA; Al-Shahi Salman R; Lip G; Brown MM; Muir K; Houlden H; Bulters DO; Galea I; Werring DJ;
    J Neurol Neurosurg Psychiatry; 2020 Mar; 91(3):298-304. PubMed ID: 31924654
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Association between haptoglobin 2-2 genotype and coronary artery disease and its severity in a tunisian population.
    Moussa A; Rejeb J; Omezzine A; Rebhi L; Boumaiza I; Kacem S; Ben Rejeb N; Boughzala E; Ben Abdelaziz A; Bouslama A
    Biochem Genet; 2014 Jun; 52(5-6):269-82. PubMed ID: 24535155
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Haptoglobin polymorphism: a novel genetic risk factor for celiac disease development and its clinical manifestations.
    Papp M; Foldi I; Nemes E; Udvardy M; Harsfalvi J; Altorjay I; Mate I; Dinya T; Varvolgyi C; Barta Z; Veres G; Lakatos PL; Tumpek J; Toth L; Szathmari E; Kapitany A; Gyetvai A; Korponay-Szabo IR
    Clin Chem; 2008 Apr; 54(4):697-704. PubMed ID: 18258668
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Association of genetic markers with coronary heart disease (myocardial infarction)--a case-control study.
    Golabi P; Kshatriya GK; Kapoor AK
    J Indian Med Assoc; 1999 Jan; 97(1):6-7. PubMed ID: 10549177
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Haptoglobin polymorphism and chronic hepatitis C.
    Louagie HK; Brouwer JT; Delanghe JR; De Buyzere ML; Leroux-Roels GG
    J Hepatol; 1996 Jul; 25(1):10-4. PubMed ID: 8836895
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Haptoglobin genotype 2-2 associated with atherosclerosis in patients with ischemic stroke.
    Merkler A; Sertić J; Bazina Martinović A; Križ T; Miličić I; Šimić M; Caban D; Ljubić H; Markeljević J; Šimičević L; Kaštelan S; Pećin I; Reiner Ž
    Gene; 2020 Aug; 752():144786. PubMed ID: 32439379
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Association between Cys282Tyr missense mutation and haptoglobin phenotype polymorphism in patients with chronic hepatitis C.
    Van Vlierberghe H; Delanghe JR; De Bie S; Praet M; De Paepe A; Messiaen L; De Vos M; Leroux-Roels G
    Eur J Gastroenterol Hepatol; 2001 Sep; 13(9):1077-81. PubMed ID: 11564959
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Effect of coronary artery bypass graft surgery on survival: overview of 10-year results from randomised trials by the Coronary Artery Bypass Graft Surgery Trialists Collaboration.
    Yusuf S; Zucker D; Peduzzi P; Fisher LD; Takaro T; Kennedy JW; Davis K; Killip T; Passamani E; Norris R
    Lancet; 1994 Aug; 344(8922):563-70. PubMed ID: 7914958
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The effect of previous coronary-artery bypass surgery on the prognosis of patients with diabetes who have acute myocardial infarction. Bypass Angioplasty Revascularization Investigation Investigators.
    Detre KM; Lombardero MS; Brooks MM; Hardison RM; Holubkov R; Sopko G; Frye RL; Chaitman BR
    N Engl J Med; 2000 Apr; 342(14):989-97. PubMed ID: 10749960
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Reference range of serum haptoglobin is haptoglobin phenotype-dependent in blacks.
    Kasvosve I; Gomo ZA; Gangaidzo IT; Mvundura E; Saungweme T; Moyo VM; Khumalo H; Boelaert JR; Gordeuk VR; Delanghe JR
    Clin Chim Acta; 2000 Jun; 296(1-2):163-70. PubMed ID: 10807979
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Haptoglobin genotypic distribution (including Hp0 allele) and associated serum haptoglobin concentrations in Koreans.
    Park KU; Song J; Kim JQ
    J Clin Pathol; 2004 Oct; 57(10):1094-5. PubMed ID: 15452167
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The prevalence of type II diabetes mellitus is haptoglobin phenotype-independent.
    Awadallah S; Hamad M
    Cytobios; 2000; 101(398):145-50. PubMed ID: 10755213
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prospective analysis after coronary-artery bypass grafting: platelet GP IIIa polymorphism (HPA-1b/PIA2) is a risk factor for bypass occlusion, myocardial infarction, and death.
    Zotz RB; Klein M; Dauben HP; Moser C; Gams E; Scharf RE
    Thromb Haemost; 2000 Mar; 83(3):404-7. PubMed ID: 10744144
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Haptoglobin phenotype and prevalent coronary heart disease in the Framingham offspring cohort.
    Levy AP; Larson MG; Corey D; Lotan R; Vita JA; Benjamin EJ
    Atherosclerosis; 2004 Feb; 172(2):361-5. PubMed ID: 15019547
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease.
    Bjornsson E; Helgason H; Halldorsson G; Helgadottir A; Gylfason A; Kehr B; Jonasdottir A; Jonasdottir A; Sigurdsson A; Oddsson A; Thorleifsson G; Magnusson OT; Gretarsdottir S; Zink F; Kristjansson RP; Asgeirsdottir M; Swinkels DW; Kiemeney LA; Eyjolfsson GI; Sigurdardottir O; Masson G; Olafsson I; Thorgeirsson G; Holm H; Thorsteinsdottir U; Gudbjartsson DF; Sulem P; Stefansson K
    Hum Mol Genet; 2017 Jun; 26(12):2364-2376. PubMed ID: 28398513
    [TBL] [Abstract][Full Text] [Related]  

  • 40. TaqMan-based real-time PCR for genotyping common polymorphisms of haptoglobin (HP1 and HP2).
    Soejima M; Koda Y
    Clin Chem; 2008 Nov; 54(11):1908-13. PubMed ID: 18787013
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.