BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

264 related articles for article (PubMed ID: 18382655)

  • 1. Maternal TLR4 and NOD2 gene variants, pro-inflammatory phenotype and susceptibility to early-onset preeclampsia and HELLP syndrome.
    van Rijn BB; Franx A; Steegers EA; de Groot CJ; Bertina RM; Pasterkamp G; Voorbij HA; Bruinse HW; Roest M
    PLoS One; 2008 Apr; 3(4):e1865. PubMed ID: 18382655
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Association of maternal Toll-like receptor-4 alleles with susceptibility to early-onset preeclampsia in central Greece.
    Vamvakopoulou DN; Satra M; Fegga A; Kourti M; Sidiropoulos A; Daponte A; Gounaris A; Syrogiannopoulos G; Vamvakopoulos NC; Sotiriou S
    Pregnancy Hypertens; 2019 Oct; 18():103-107. PubMed ID: 31586781
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Epistatic interaction between TLR4 and NOD2 in patients with Crohn's Disease: relation with risk and phenotype in a Spanish cohort.
    Martinez-Chamorro A; Moreno A; Gómez-García M; Cabello MJ; Martin J; Lopez-Nevot MÁ
    Immunobiology; 2016 Sep; 221(9):927-33. PubMed ID: 27290609
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease.
    Rigoli L; Romano C; Caruso RA; Lo Presti MA; Di Bella C; Procopio V; Lo Giudice G; Amorini M; Costantino G; Sergi MD; Cuppari C; Calabro GE; Gallizzi R; Salpietro CD; Fries W
    World J Gastroenterol; 2008 Jul; 14(28):4454-61. PubMed ID: 18680223
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Common NOD2/CARD15 and TLR4 Polymorphisms Are Associated with Crohn's Disease Phenotypes in Southeastern Brazilians.
    Tolentino YF; Elia PP; Fogaça HS; Carneiro AJ; Zaltman C; Moura-Neto R; Luiz RR; Carvalho Mda G; de Souza HS
    Dig Dis Sci; 2016 Sep; 61(9):2636-47. PubMed ID: 27107867
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Microarray profiling reveals that placental transcriptomes of early-onset HELLP syndrome and preeclampsia are similar.
    Várkonyi T; Nagy B; Füle T; Tarca AL; Karászi K; Schönléber J; Hupuczi P; Mihalik N; Kovalszky I; Rigó J; Meiri H; Papp Z; Romero R; Than NG
    Placenta; 2011 Feb; 32 Suppl(0):S21-9. PubMed ID: 20541258
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic association and phenotypic correlation of TLR4 but not NOD2 variants with Tunisian inflammatory bowel disease.
    Feki S; Bouzid D; Abida O; Chtourou L; Elloumi N; Toumi A; Hachicha H; Amouri A; Tahri N; Masmoudi H
    J Dig Dis; 2017 Nov; 18(11):625-633. PubMed ID: 29055077
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association between tumor necrosis factor (TNF)-alpha G-308A gene polymorphism and preeclampsia complicated by severe fetal growth restriction.
    Molvarec A; Jermendy A; Nagy B; Kovács M; Várkonyi T; Hupuczi P; Prohászka Z; Rigó J
    Clin Chim Acta; 2008 Jun; 392(1-2):52-7. PubMed ID: 18396154
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic aspects of preeclampsia and the HELLP syndrome.
    Haram K; Mortensen JH; Nagy B
    J Pregnancy; 2014; 2014():910751. PubMed ID: 24991435
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Toll-like receptor gene polymorphisms and preeclampsia risk: a case-control study and data synthesis.
    Xie F; Hu Y; Speert DP; Turvey SE; Peng G; Money DM; Magee LA; von Dadelszen P;
    Hypertens Pregnancy; 2010; 29(4):390-8. PubMed ID: 20818954
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Severe preeclampsia is associated with a positive family history of hypertension and hypercholesterolemia.
    Roes EM; Sieben R; Raijmakers MT; Peters WH; Steegers EA
    Hypertens Pregnancy; 2005; 24(3):259-71. PubMed ID: 16263598
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular genetics of preeclampsia and HELLP syndrome - a review.
    Jebbink J; Wolters A; Fernando F; Afink G; van der Post J; Ris-Stalpers C
    Biochim Biophys Acta; 2012 Dec; 1822(12):1960-9. PubMed ID: 22917566
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A comparison of the diagnostic utility of the sFlt-1/PlGF ratio versus PlGF alone for the detection of preeclampsia/HELLP syndrome.
    Stepan H; Hund M; Gencay M; Denk B; Dinkel C; Kaminski WE; Wieloch P; Semus B; Meloth T; Dröge LA; Verlohren S
    Hypertens Pregnancy; 2016 Aug; 35(3):295-305. PubMed ID: 27028698
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Proteasome Levels and Activity in Pregnancies Complicated by Severe Preeclampsia and Hemolysis, Elevated Liver Enzymes, and Thrombocytopenia (HELLP) Syndrome.
    Berryman K; Buhimschi CS; Zhao G; Axe M; Locke M; Buhimschi IA
    Hypertension; 2019 Jun; 73(6):1308-1318. PubMed ID: 31067191
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Toll-like receptor 4 and NOD2/CARD15 mutations in Hungarian patients with Crohn's disease: phenotype-genotype correlations.
    Lakatos PL; Lakatos L; Szalay F; Willheim-Polli C; Osterreicher C; Tulassay Z; Molnar T; Reinisch W; Papp J; Mozsik G; Ferenci P;
    World J Gastroenterol; 2005 Mar; 11(10):1489-95. PubMed ID: 15770725
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Elastic properties of ascending aorta and ventricular-arterial coupling in women with previous pregnancy complicated by HELLP syndrome.
    Sciatti E; Orabona R; Prefumo F; Vizzardi E; Bonadei I; Valcamonico A; Metra M; Frusca T
    J Hypertens; 2019 Feb; 37(2):356-364. PubMed ID: 30234780
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Screening for G1528C mutation in mitochondrial trifunctional protein gene in pregnant women with severe preeclampsia and new born infant].
    Wang R; Yang Z; Zhu JM; Wang JL; Yang HX; Wang Q; Zhai GR; Li Z; Yu M
    Zhonghua Fu Chan Ke Za Zhi; 2006 Oct; 41(10):672-5. PubMed ID: 17199921
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Maternal immune suppression during pregnancy does not prevent abnormal behavior in offspring.
    Griffin A; Bowles T; Solis L; Railey T; Beauti S; Robinson R; Spencer SK; Shaffery JP; Wallace K
    Biol Sex Differ; 2024 Mar; 15(1):27. PubMed ID: 38532505
    [TBL] [Abstract][Full Text] [Related]  

  • 19. TLR4 and NOD2/CARD15 genetic polymorphisms and their possible role in gastric carcinogenesis.
    Rigoli L; Di Bella C; Fedele F; Procopio V; Amorini M; Lo Giudice G; Romeo P; Pugliatti F; Finocchiaro G; Lucianò R; Caruso RA
    Anticancer Res; 2010 Feb; 30(2):513-7. PubMed ID: 20332463
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CDKN1C mutations in HELLP/preeclamptic mothers of Beckwith-Wiedemann Syndrome (BWS) patients.
    Romanelli V; Belinchón A; Campos-Barros A; Heath KE; García-Miñaur S; Martínez-Glez V; Palomo R; Mercado G; Gracia R; Lapunzina P
    Placenta; 2009 Jun; 30(6):551-4. PubMed ID: 19386358
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.