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PUBMED FOR HANDHELDS

Journal Abstract Search


279 related items for PubMed ID: 26135579

  • 41. Association of of IL-1 receptor antagonist (IL-1RN) and interleukin-1β genes (IL-1β) polymorphisms with recurrent pregnancy loss in Iranian Azeri women.
    Ali Rahmani S, Paknejad Z, Mohammadkhanlou M, Daneshparvar M.
    Horm Mol Biol Clin Investig; 2017 Dec 27; 33(3):. PubMed ID: 29281611
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  • 42. Implications of VEGF gene sequence variations and its expression in recurrent pregnancy loss.
    Amin I, Pandith AA, Manzoor U, Mir SH, Afroze D, Koul AM, Wani S, Ahmad A, Qasim I, Rashid M, Wani UM, Anwar I, Aein QU, Mansoor S.
    Reprod Biomed Online; 2021 Dec 27; 43(6):1035-1044. PubMed ID: 34716101
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  • 43. Association of genetic polymorphisms in VEGF -460, -7 and -583 and hematocrit level with the development of idiopathic recurrent pregnancy loss and a meta-analysis.
    Jung YW, Ahn EH, Kim JO, An HJ, Cho SH, Kim YR, Lee WS, Kim NK.
    J Gene Med; 2018 Sep 27; 20(9):e3048. PubMed ID: 30088835
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  • 44. Association of Human forkhead box protein 3 (FOXP3) gene polymorphisms with idiopathic recurrent pregnancy loss among Kazakhstani women.
    Abdukassimova M, Kanabekova P, Bauyrzhanova Z, Ukybassova T, Kaldygulova L, Imankulova B, Aimagambetova G, Almawi WY.
    Gene; 2021 Oct 30; 801():145835. PubMed ID: 34274475
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  • 45. Annexin V expression in human placenta is influenced by the carriership of the common haplotype M2.
    Chinni E, Tiscia GL, Colaizzo D, Vergura P, Margaglione M, Grandone E.
    Fertil Steril; 2009 Mar 30; 91(3):940-2. PubMed ID: 18462735
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  • 46. Association of Methylenetetrahydrofolate Reductase C677T and A1298C Gene Polymorphisms With Recurrent Pregnancy Loss in Syrian Women.
    Al-Achkar W, Wafa A, Ammar S, Moassass F, Jarjour RA.
    Reprod Sci; 2017 Sep 30; 24(9):1275-1279. PubMed ID: 28814189
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  • 47. Methylenetetrahydrofolate reductase gene polymorphisms in Egyptian women with unexplained recurrent pregnancy loss.
    Settin A, Elshazli R, Salama A, ElBaz R.
    Genet Test Mol Biomarkers; 2011 Dec 30; 15(12):887-92. PubMed ID: 21815801
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  • 48. Precision Medicine in Assisted Conception: A Multicenter Observational Treatment Cohort Study of the Annexin A5 M2 Haplotype as a Biomarker for Antithrombotic Treatment to Improve Pregnancy Outcome.
    Fishel S, Baker D, Elson J, Ragunath M, Atkinson G, Shaker A, Omar A, Kazem R, Beccles A, Greer IA.
    EBioMedicine; 2016 Aug 30; 10():298-304. PubMed ID: 27440469
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  • 49. Functional characterization of annexin A5 gene promoter allelic variants.
    Tiscia GL, Dørum E, Myklebust CF, Grandone E, Sandset PM, Skretting G.
    Thromb Res; 2016 Aug 30; 144():93-9. PubMed ID: 27318245
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  • 50. Interleukin-18 promoter polymorphisms and risk of idiopathic recurrent pregnancy loss in a Tunisian population.
    Messaoudi S, Dandana M, Magdoud K, Meddeb S, Ben Slama N, Hizem S, Mahjoub T.
    J Reprod Immunol; 2012 Mar 30; 93(2):109-13. PubMed ID: 22386125
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  • 51. Contribution of ADIPOQ Variants to the Genetic Susceptibility of Recurrent Pregnancy Loss.
    Bahia W, Soltani I, Haddad A, Radhouani A, Mahdhi A, Ferchichi S, Almawi WY.
    Reprod Sci; 2021 Jan 30; 28(1):263-270. PubMed ID: 32748222
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  • 52. Lessons From the EThIGII Trial: Proper Putative Benefit Assessment of Low-Molecular-Weight Heparin Treatment in M2/ANXA5 Haplotype Carriers.
    Rogenhofer N, Markoff A, Wagner A, Klein HG, Petroff D, Schleussner E, EThIG II Group, Thaler CJ.
    Clin Appl Thromb Hemost; 2017 Jan 30; 23(1):27-33. PubMed ID: 27418639
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  • 53. Chorionic gonadotropin beta-gene variants are associated with recurrent miscarriage in two European populations.
    Rull K, Nagirnaja L, Ulander VM, Kelgo P, Margus T, Kaare M, Aittomäki K, Laan M.
    J Clin Endocrinol Metab; 2008 Dec 30; 93(12):4697-706. PubMed ID: 18782867
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  • 54. Annexin A5 haplotypes in familial hypercholesterolemia: lack of association with carotid intima-media thickness and cardiovascular disease risk.
    Hiddink L, Dallinga-Thie GM, Hovingh GK, de Visser MC, Peer PG, Stalenhoef AF, van Heerde WL.
    Atherosclerosis; 2015 Feb 30; 238(2):195-200. PubMed ID: 25525746
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  • 55. Interleukin-1 gene cluster variants and recurrent pregnancy loss among North Indian women: retrospective study and meta-analysis.
    Agrawal S, Parveen F, Faridi RM, Prakash S.
    Reprod Biomed Online; 2012 Mar 30; 24(3):342-51. PubMed ID: 22285242
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  • 56. The correlation of estrogen receptor 1 and progesterone receptor genes polymorphisms with recurrent pregnancy loss in a cohort of Egyptian women.
    Refeat MM, Shalabi T, El-Bassyouni HT, Shaker M.
    Mol Biol Rep; 2021 May 30; 48(5):4413-4420. PubMed ID: 34061327
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  • 57. Association Study between the Polymorphisms of Matrix Metalloproteinase (MMP) Genes and Idiopathic Recurrent Pregnancy Loss.
    Park HS, Ko KH, Kim JO, An HJ, Kim YR, Kim JH, Lee WS, Kim NK.
    Genes (Basel); 2019 May 07; 10(5):. PubMed ID: 31067818
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  • 58. The association between polymorphisms of genes related to inflammation and recurrent pregnancy loss.
    Gu Y, Wang JM, Zhang ZF, Wang J, Cao YL, Pan CJ, Yin LR, Du J.
    Gynecol Endocrinol; 2018 Apr 07; 34(4):349-352. PubMed ID: 29084471
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  • 59. Study of the Association Between microRNA (miR-25T>C, miR-32C>A, miR-125C>T, and miR-222G>T) Polymorphisms and the Risk of Recurrent Pregnancy Loss in Korean Women.
    Lee JY, Kim JO, Park HS, Ryu CS, Kim JH, Kim YR, Lee WS, Lee JR, Kim NK.
    Genes (Basel); 2020 Mar 26; 11(4):. PubMed ID: 32224893
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  • 60. HLA-DRB1 polymorphism in recurrent pregnancy loss: New evidence for an association to HLA-DRB1*07.
    Thomsen CK, Steffensen R, Nielsen HS, Kolte AM, Krog MC, Egerup P, Larsen EC, Hviid TV, Christiansen OB.
    J Reprod Immunol; 2021 Jun 26; 145():103308. PubMed ID: 33725525
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