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 *

119 related articles for article (PubMed ID: 23580146)

  • 21. Multicity study of air pollution and mortality in Latin America (the ESCALA study).
    Romieu I; Gouveia N; Cifuentes LA; de Leon AP; Junger W; Vera J; Strappa V; Hurtado-Díaz M; Miranda-Soberanis V; Rojas-Bracho L; Carbajal-Arroyo L; Tzintzun-Cervantes G;
    Res Rep Health Eff Inst; 2012 Oct; (171):5-86. PubMed ID: 23311234
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genetically reduced antioxidative protection and increased ischemic heart disease risk: The Copenhagen City Heart Study.
    Juul K; Tybjaerg-Hansen A; Marklund S; Heegaard NH; Steffensen R; Sillesen H; Jensen G; Nordestgaard BG
    Circulation; 2004 Jan; 109(1):59-65. PubMed ID: 14662715
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Common genetic markers and prediction of recurrent events after ischemic stroke in young adults.
    Pezzini A; Grassi M; Del Zotto E; Lodigiani C; Ferrazzi P; Spalloni A; Patella R; Giossi A; Volonghi I; Iacoviello L; Magoni M; Rota LL; Rasura M; Padovani A
    Neurology; 2009 Sep; 73(9):717-23. PubMed ID: 19720979
    [TBL] [Abstract][Full Text] [Related]  

  • 24. THAOS - The Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis.
    Coelho T; Maurer MS; Suhr OB
    Curr Med Res Opin; 2013 Jan; 29(1):63-76. PubMed ID: 23193944
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Sex differentials in life expectancy and mortality in developed countries: an analysis by age groups and causes of death from recent and historical data.
    United Nations. Department of International Economic and Social Affairs. Population Division
    Popul Bull UN; 1988; 25():65-107. PubMed ID: 12315555
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Association of cluster of differentiation 36 gene variant rs1761667 (G>A) with metabolic syndrome in Egyptian adults.
    Bayoumy NM; El-Shabrawi MM; Hassan HH
    Saudi Med J; 2012 May; 33(5):489-94. PubMed ID: 22588808
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The frequency of Klotho KL-VS polymorphism in a large Italian population, from young subjects to centenarians, suggests the presence of specific time windows for its effect.
    Invidia L; Salvioli S; Altilia S; Pierini M; Panourgia MP; Monti D; De Rango F; Passarino G; Franceschi C
    Biogerontology; 2010 Feb; 11(1):67-73. PubMed ID: 19421891
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Haplotypes and DNA sequence variation within and surrounding the transthyretin gene: genotype-phenotype correlations in familial amyloid polyneuropathy (V30M) in Portugal and Sweden.
    Soares ML; Coelho T; Sousa A; Holmgren G; Saraiva MJ; Kastner DL; Buxbaum JN
    Eur J Hum Genet; 2004 Mar; 12(3):225-37. PubMed ID: 14673473
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The global impact of noncommunicable diseases: estimates and projections.
    Manton KG
    World Health Stat Q; 1988; 41(3-4):255-66. PubMed ID: 3232413
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Native state kinetic stabilization as a strategy to ameliorate protein misfolding diseases: a focus on the transthyretin amyloidoses.
    Johnson SM; Wiseman RL; Sekijima Y; Green NS; Adamski-Werner SL; Kelly JW
    Acc Chem Res; 2005 Dec; 38(12):911-21. PubMed ID: 16359163
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prevalence of germline mutations in the TTR gene in a consecutive series of surgical pathology specimens with ATTR amyloid.
    Eriksson M; Büttner J; Todorov T; Yumlu S; Schönland S; Hegenbart U; Kristen AV; Dengler T; Lohse P; Helmke B; Schmidt H; Röcken C
    Am J Surg Pathol; 2009 Jan; 33(1):58-65. PubMed ID: 18830126
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Impact of the 1990 Hong Kong legislation for restriction on sulfur content in fuel.
    Wong CM; Rabl A; Thach TQ; Chau YK; Chan KP; Cowling BJ; Lai HK; Lam TH; McGhee SM; Anderson HR; Hedley AJ
    Res Rep Health Eff Inst; 2012 Aug; (170):5-91. PubMed ID: 23316618
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Polymorphic markers in the SRD5A2 gene and prostate cancer risk: a population-based case-control study.
    Hsing AW; Chen C; Chokkalingam AP; Gao YT; Dightman DA; Nguyen HT; Deng J; Cheng J; Sesterhenn IA; Mostofi FK; Stanczyk FZ; Reichardt JK
    Cancer Epidemiol Biomarkers Prev; 2001 Oct; 10(10):1077-82. PubMed ID: 11588134
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetic susceptibility to cerebrovascular disease: A systematic review.
    Griessenauer CJ; Farrell S; Sarkar A; Zand R; Abedi V; Holland N; Michael A; Cummings CL; Metpally R; Carey DJ; Goren O; Martin N; Hendrix P; Schirmer CM
    J Cereb Blood Flow Metab; 2018 Nov; 38(11):1853-1871. PubMed ID: 30182779
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Life expectancies among survivors of acute cerebrovascular disease.
    Hannerz H; Nielsen ML
    Stroke; 2001 Aug; 32(8):1739-44. PubMed ID: 11486099
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Determinants of transthyretin levels and their association with adverse clinical outcomes among UK Biobank participants.
    Shetty NS; Gaonkar M; Patel N; Pampana A; Vekariya N; Li P; Arora G; Arora P
    Nat Commun; 2024 Jul; 15(1):6221. PubMed ID: 39043640
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The thrombomodulin gene mutation G(127)-->A (Ala25Thr) and cerebrovascular disease.
    Warner D; Catto A; Kunz G; Ireland H; Grant PJ; Lane DA
    Cerebrovasc Dis; 2000; 10(5):359-63. PubMed ID: 10971021
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Prediction in cerebrovascular diseases].
    Hamann GF
    Nervenarzt; 2014 Oct; 85(10):1269-79. PubMed ID: 25292162
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Evaluation of common unfavourable genetic variants in cerebrovascular diseases: recommendation for supportive genetic examinations and methodological approaches for common genetic variants.
    Szolnoki Z
    Curr Med Chem; 2009; 16(24):3168-73. PubMed ID: 19689290
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetic susceptibility to cerebrovascular disease.
    Della-Morte D; Pacifici F; Rundek T
    Curr Opin Lipidol; 2016 Apr; 27(2):187-95. PubMed ID: 26959706
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.