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 *

120 related articles for article (PubMed ID: 32954288)

  • 21. 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]  

  • 22. Transmission properties of atypical Creutzfeldt-Jakob disease: a clue to disease etiology?
    Kobayashi A; Parchi P; Yamada M; Brown P; Saverioni D; Matsuura Y; Takeuchi A; Mohri S; Kitamoto T
    J Virol; 2015 Apr; 89(7):3939-46. PubMed ID: 25609817
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein.
    Hainfellner JA; Parchi P; Kitamoto T; Jarius C; Gambetti P; Budka H
    Ann Neurol; 1999 Jun; 45(6):812-6. PubMed ID: 10360778
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia.
    Parchi P; Capellari S; Gambetti P
    Microsc Res Tech; 2000 Jul; 50(1):16-25. PubMed ID: 10871544
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease.
    Galeno R; Di Bari MA; Nonno R; Cardone F; Sbriccoli M; Graziano S; Ingrosso L; Fiorini M; Valanzano A; Pasini G; Poleggi A; Vinci R; Ladogana A; Puopolo M; Monaco S; Agrimi U; Zanusso G; Pocchiari M
    J Virol; 2017 Jun; 91(11):. PubMed ID: 28298604
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease.
    Gabizon R; Rosenman H; Meiner Z; Kahana I; Kahana E; Shugart Y; Ott J; Prusiner SB
    Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):385-90. PubMed ID: 7913755
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob disease.
    Nihat A; Ranson JM; Harris D; McNiven K; Mok T; Rudge P; Collinge J; Llewellyn DJ; Mead S
    Brain Commun; 2022; 4(4):fcac201. PubMed ID: 35974795
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene.
    Ito Y; Sanjo N; Hizume M; Kobayashi A; Ohgami T; Satoh K; Hamaguchi T; Yamada M; Kitamoto T; Mizusawa H; Yokota T
    Biochem Biophys Res Commun; 2018 Feb; 496(4):1055-1061. PubMed ID: 29382530
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Association between the M129V variant allele of PRNP gene and mild temporal lobe epilepsy in women.
    Labate A; Manna I; Gambardella A; Le Piane E; La Russa A; Condino F; Cittadella R; Aguglia U; Quattrone A
    Neurosci Lett; 2007 Jun; 421(1):1-4. PubMed ID: 17092648
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Epidemiological genetics and meta-analysis of a polymorphism at codon 129 of the PRNP gene in Alzheimer's disease in Brazil.
    Pimentel LF; Gomes da Cunha JE; Morelato RL; de Paula F; de Oliveira JR
    Neurol Res; 2014 Sep; 36(9):775-8. PubMed ID: 24620982
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease.
    Erginel-Unaltuna N; Peoc'h K; Komurcu E; Acuner TT; Issever H; Laplanche JL
    Eur J Hum Genet; 2001 Dec; 9(12):965-8. PubMed ID: 11840201
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2.
    Samman I; Schulz-Schaeffer WJ; Wöhrle JC; Sommer A; Kretzschmar HA; Hennerici M
    J Neurol Neurosurg Psychiatry; 1999 Nov; 67(5):678-81. PubMed ID: 10519881
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 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. Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob disease.
    Cervenáková L; Goldfarb LG; Garruto R; Lee HS; Gajdusek DC; Brown P
    Proc Natl Acad Sci U S A; 1998 Oct; 95(22):13239-41. PubMed ID: 9789072
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Novel PRNP mutation in a patient with a slow progressive dementia syndrome.
    Heinemann U; Krasnianski A; Meissner B; Grasbon-Frodl EM; Kretzschmar HA; Zerr I
    Med Sci Monit; 2008 May; 14(5):CS41-43. PubMed ID: 18443555
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Polymorphism at codon 129 of the prion protein gene determines cerebellar pathology in Creutzfeldt-Jakob disease.
    Schulz-Schaeffer WJ; Giese A; Windl O; Kretzschmar HA
    Clin Neuropathol; 1996; 15(6):353-7. PubMed ID: 8937783
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.
    Pastore M; Chin SS; Bell KL; Dong Z; Yang Q; Yang L; Yuan J; Chen SG; Gambetti P; Zou WQ
    Am J Pathol; 2005 Dec; 167(6):1729-38. PubMed ID: 16314483
    [TBL] [Abstract][Full Text] [Related]  

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