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 *

122 related articles for article (PubMed ID: 17092648)

  • 21. Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysis.
    Del Bo R; Scarlato M; Ghezzi S; Martinelli-Boneschi F; Fenoglio C; Galimberti G; Galbiati S; Virgilio R; Galimberti D; Ferrarese C; Scarpini E; Bresolin N; Comi GP
    Neurobiol Aging; 2006 May; 27(5):770.e1-770.e5. PubMed ID: 16099550
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Genetic association study of the HLA class II alleles DRB1, DQA1, and DQB1 in patients with pharmacoresistant temporal lobe epilepsy associated with mesial hippocampal sclerosis.
    Horta WG; Paradela E; Figueiredo A; Meira ID; Pereira VC; Rego CC; Oliveira R; Andraus ME; de Lacerda GC; Moura P; de Souza JP; Paiva CL; Alves-Leon SV
    Seizure; 2015 Sep; 31():7-11. PubMed ID: 26362370
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Serotonin transporter gene (5-Htt): association analysis with temporal lobe epilepsy.
    Manna I; Labate A; Gambardella A; Forabosco P; La Russa A; Le Piane E; Aguglia U; Quattrone A
    Neurosci Lett; 2007 Jun; 421(1):52-6. PubMed ID: 17548158
    [TBL] [Abstract][Full Text] [Related]  

  • 25. GABA receptor 1 polymorphism (G1465A) and temporal lobe epilepsy.
    Salzmann A; Moulard B; Crespel A; Baldy-Moulinier M; Buresi C; Malafosse A
    Epilepsia; 2005 Jun; 46(6):931-3. PubMed ID: 15946333
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The 129 codon polymorphism of the prion protein gene influences earlier cognitive performance in Down syndrome subjects.
    Del Bo R; Comi GP; Giorda R; Crimi M; Locatelli F; Martinelli-Boneschi F; Pozzoli U; Castelli E; Bresolin N; Scarlato G
    J Neurol; 2003 Jun; 250(6):688-92. PubMed ID: 12796830
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease.
    Poleggi A; Bizzarro A; Acciarri A; Antuono P; Bagnoli S; Cellini E; Forno GD; Giannattasio C; Lauria A; Matera MG; Nacmias B; Puopolo M; Seripa D; Sorbi S; Wekstein DR; Pocchiari M; Masullo C
    Eur J Neurol; 2008 Feb; 15(2):173-8. PubMed ID: 18217885
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The human prion gene M129V polymorphism is not associated with idiopathic Parkinson's disease in three distinct populations.
    Scholz SW; Xiromerisiou G; Fung HC; Eerola J; Hellström O; Papadimitriou A; Hadjigeorgiou GM; Tienari PJ; Fernandez HH; Mandel R; Okun MS; Gwinn-Hardy K; Singleton AB
    Neurosci Lett; 2006 Mar; 395(3):227-9. PubMed ID: 16298483
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Association of KEAP1 and NFE2L2 polymorphisms with temporal lobe epilepsy and drug resistant epilepsy.
    Liu Z; Yin X; Liu L; Tao H; Zhou H; Ma G; Cui L; Li Y; Zhang S; Xu Z; Yao L; Cai Z; Zhao B; Li K
    Gene; 2015 Oct; 571(2):231-6. PubMed ID: 26149655
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Polymorphisms at codons 129 and 219 of the prion protein gene (PRNP) are not associated with sporadic Alzheimer's disease in the Korean population.
    Jeong BH; Lee KH; Jeong YE; Hwang KA; Lee YJ; Carp RI; Ju YR; Kim YS
    Eur J Neurol; 2007 Jun; 14(6):621-6. PubMed ID: 17539938
    [TBL] [Abstract][Full Text] [Related]  

  • 31. GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy.
    Gambardella A; Manna I; Labate A; Chifari R; La Russa A; Serra P; Cittadella R; Bonavita S; Andreoli V; LePiane E; Sasanelli F; Di Costanzo A; Zappia M; Tedeschi G; Aguglia U; Quattrone A
    Neurology; 2003 Feb; 60(4):560-3. PubMed ID: 12601092
    [TBL] [Abstract][Full Text] [Related]  

  • 32. No evidence for a role of the coding variant of the Toll-like receptor 4 gene in temporal lobe epilepsy.
    Manna I; Labate A; Mumoli L; Ferlazzo E; Aguglia U; Quattrone A; Gambardella A
    Seizure; 2013 Nov; 22(9):791-3. PubMed ID: 23810712
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Codon 129 polymorphism of prion protein gene in is not a risk factor for Alzheimer's disease.
    Smid J; Landemberger MC; Bahia VS; Martins VR; Nitrini R
    Arq Neuropsiquiatr; 2013 Jul; 71(7):423-7. PubMed ID: 23857619
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The normal distribution of PRNP codon 129 polymorphism in the Moroccan population (Arabs and Casablanca residents).
    Nadifi S; Slassi I; Hachimi KM; Gazzaz B; Bellayou H; Raddaoui K; Laplanche JL
    Pathol Biol (Paris); 2008 May; 56(3):133-6. PubMed ID: 18191917
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Survival in Alzheimer's disease is shorter in women carrying heterozygosity at codon 129 of the PRNP gene and no APOE epsilon 4 allele.
    Giannattasio C; Poleggi A; Puopolo M; Pocchiari M; Antuono P; Dal Forno G; Wekstein DR; Matera MG; Seripa D; Acciarri A; Bizzarro A; Lauria A; Masullo C
    Dement Geriatr Cogn Disord; 2008; 25(4):354-8. PubMed ID: 18332630
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype.
    Lee HS; Brown P; Cervenáková L; Garruto RM; Alpers MP; Gajdusek DC; Goldfarb LG
    J Infect Dis; 2001 Jan; 183(2):192-196. PubMed ID: 11120925
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Absence of association between codon 129/219 polymorphisms of the prion protein gene and Alzheimer's disease in Japan.
    Ohkubo T; Sakasegawa Y; Asada T; Kinoshita T; Goto Y; Kimura H; Mizusawa H; Hachiya NS; Kaneko K
    Ann Neurol; 2003 Oct; 54(4):553-4; author reply 555. PubMed ID: 14520676
    [No Abstract]   [Full Text] [Related]  

  • 38. The GABBR1 locus and the G1465A variant is not associated with temporal lobe epilepsy preceded by febrile seizures.
    Ma S; Abou-Khalil B; Sutcliffe JS; Haines JL; Hedera P
    BMC Med Genet; 2005 Mar; 6():13. PubMed ID: 15799783
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A polymorphism in CALHM1 is associated with temporal lobe epilepsy.
    Lv RJ; He JS; Fu YH; Shao XQ; Wu LW; Lu Q; Jin LR; Liu H
    Epilepsy Behav; 2011 Apr; 20(4):681-5. PubMed ID: 21439911
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Does the clinical phenotype of fatal familial insomnia depend on PRNP codon 129 methionine-valine polymorphism?
    Rupprecht S; Grimm A; Schultze T; Zinke J; Karvouniari P; Axer H; Witte OW; Schwab M
    J Clin Sleep Med; 2013 Dec; 9(12):1343-5. PubMed ID: 24340298
    [TBL] [Abstract][Full Text] [Related]  

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