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 *

183 related articles for article (PubMed ID: 21838916)

  • 1. The first report of RPSA polymorphisms, also called 37/67 kDa LRP/LR gene, in sporadic Creutzfeldt-Jakob disease (CJD).
    Yun J; Jin HT; Lee YJ; Choi EK; Carp RI; Jeong BH; Kim YS
    BMC Med Genet; 2011 Aug; 12():108. PubMed ID: 21838916
    [TBL] [Abstract][Full Text] [Related]  

  • 2. RARB and STMN2 polymorphisms are not associated with sporadic Creutzfeldt-Jakob disease (CJD) in the Korean population.
    Jeong BH; Kim HJ; Lee KH; Carp RI; Kim YS
    Mol Biol Rep; 2014; 41(4):2389-95. PubMed ID: 24414001
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Lack of association between 14-3-3 beta gene (YWHAB) polymorphisms and sporadic Creutzfeldt-Jakob disease (CJD).
    Jeong BH; Jin HT; Choi EK; Carp RI; Kim YS
    Mol Biol Rep; 2012 Dec; 39(12):10647-53. PubMed ID: 23053962
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1.
    Mead S; Mahal SP; Beck J; Campbell T; Farrall M; Fisher E; Collinge J
    Am J Hum Genet; 2001 Dec; 69(6):1225-35. PubMed ID: 11704923
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Polymorphisms at codons 56 and 174 of the prion-like protein gene (PRND) are not associated with sporadic Creutzfeldt-Jakob disease.
    Jeong BH; Kim NH; Kim JI; Carp RI; Kim YS
    J Hum Genet; 2005; 50(6):311-314. PubMed ID: 15933804
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The First Meta-Analysis of the M129V Single-Nucleotide Polymorphism (SNP) of the Prion Protein Gene (
    Kim YC; Jeong BH
    Cells; 2021 Nov; 10(11):. PubMed ID: 34831353
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease.
    Croes EA; Alizadeh BZ; Bertoli-Avella AM; Rademaker T; Vergeer-Drop J; Dermaut B; Houwing-Duistermaat JJ; Wientjens DP; Hofman A; Van Broeckhoven C; van Duijn CM
    Eur J Hum Genet; 2004 May; 12(5):389-94. PubMed ID: 14970845
    [TBL] [Abstract][Full Text] [Related]  

  • 8. PRNP 1368 polymorphism is not associated with sporadic Creutzfeldt-Jakob disease in the Korean population.
    Jeong BH; Lee KH; Lee YJ; Kim YH; Cho YS; Carp RI; Kim YS
    Eur J Neurol; 2008 Aug; 15(8):846-50. PubMed ID: 18549395
    [TBL] [Abstract][Full Text] [Related]  

  • 9. PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.
    Bishop MT; Pennington C; Heath CA; Will RG; Knight RS
    BMC Med Genet; 2009 Dec; 10():146. PubMed ID: 20035629
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Absence of association between two HECTD2 polymorphisms and sporadic Creutzfeldt-Jakob disease.
    Jeong BH; Lee KH; Lee YJ; Yun J; Park YJ; Cho HJ; Kim YH; Cho YS; Choi EK; Carp RI; Kim YS
    Dement Geriatr Cogn Disord; 2011; 31(2):146-51. PubMed ID: 21335971
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A polymorphism in the YWHAH gene encoding 14-3-3 eta that is not associated with sporadic Creutzfeldt-Jakob disease (CJD).
    Yun J; Jeong BH; Kim HJ; Park YJ; Lee YJ; Choi EK; Carp RI; Kim YS
    Mol Biol Rep; 2012 Apr; 39(4):3619-25. PubMed ID: 21739144
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Polymorphism at 3' UTR +28 of the prion-like protein gene is associated with sporadic Creutzfeldt-Jakob disease.
    Jeong BH; Kim NH; Choi EK; Lee C; Song YH; Kim JI; Carp RI; Kim YS
    Eur J Hum Genet; 2005 Sep; 13(9):1094-7. PubMed ID: 15986038
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association of sporadic Creutzfeldt-Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean population.
    Jeong BH; Lee KH; Kim NH; Jin JK; Kim JI; Carp RI; Kim YS
    Neurogenetics; 2005 Dec; 6(4):229-32. PubMed ID: 16217673
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cloning and characterization of full-length coding sequence (CDS) of the ovine 37/67-kDa laminin receptor (RPSA).
    Qiao J; Su X; Wang Y; Yang J; Kouadir M; Zhou X; Yin X; Zhao D
    Mol Biol Rep; 2009 Nov; 36(8):2131-7. PubMed ID: 19105045
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Regulatory sequences of the PRNP gene influence susceptibility to sporadic Creutzfeldt-Jakob disease.
    Bratosiewicz-Wasik J; Liberski PP; Golanska E; Jansen GH; Wasik TJ
    Neurosci Lett; 2007 Jan; 411(3):163-7. PubMed ID: 17134829
    [TBL] [Abstract][Full Text] [Related]  

  • 16. PRNP contains both intronic and upstream regulatory regions that may influence susceptibility to Creutzfeldt-Jakob Disease.
    McCormack JE; Baybutt HN; Everington D; Will RG; Ironside JW; Manson JC
    Gene; 2002 Apr; 288(1-2):139-46. PubMed ID: 12034503
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Significant association of a M129V independent polymorphism in the 5' UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study.
    Vollmert C; Windl O; Xiang W; Rosenberger A; Zerr I; Wichmann HE; Bickeböller H; Illig T; ; Kretzschmar HA
    J Med Genet; 2006 Oct; 43(10):e53. PubMed ID: 17047093
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease.
    Salvatore M; Genuardi M; Petraroli R; Masullo C; D'Alessandro M; Pocchiari M
    Hum Genet; 1994 Oct; 94(4):375-9. PubMed ID: 7927332
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic association of a cathepsin D polymorphism and sporadic Creutzfeldt-Jakob disease.
    Jeong BH; Lee KH; Lee YJ; Yun J; Park YJ; Bae Y; Kim YH; Cho YS; Choi EK; Carp RI; Kim YS
    Dement Geriatr Cogn Disord; 2009; 28(4):302-6. PubMed ID: 19828951
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lack of association between PRNP 1368 polymorphism and Alzheimer's disease or vascular dementia.
    Jeong BH; Lee KH; Lee YJ; Kim YJ; Choi EK; Kim YH; Cho YS; Carp RI; Kim YS
    BMC Med Genet; 2009 Apr; 10():32. PubMed ID: 19351416
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.