120 related articles for article (PubMed ID: 32954288)
1. Prion protein codon 129 polymorphism in mild cognitive impairment and dementia: the Rotterdam Study.
Karamujić-Čomić H; Ahmad S; Lysen TS; Heshmatollah A; Roshchupkin GV; Vernooij MW; Rozemuller AJM; Ikram MA; Amin N; van Duijn CM
Brain Commun; 2020; 2(1):fcaa030. PubMed ID: 32954288
[TBL] [Abstract][Full Text] [Related]
2. [Genetic background of human prion diseases].
Kovács GG
Ideggyogy Sz; 2007 Nov; 60(11-12):438-46. PubMed ID: 18198790
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Polymorphisms of the prion protein gene (PRNP) in a Korean population.
Jeong BH; Nam JH; Lee YJ; Lee KH; Jang MK; Carp RI; Lee HD; Ju YR; Ahn Jo S; Park KY; Kim YS
J Hum Genet; 2004; 49(6):319-324. PubMed ID: 15148589
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.
Parchi P; Castellani R; Capellari S; Ghetti B; Young K; Chen SG; Farlow M; Dickson DW; Sima AA; Trojanowski JQ; Petersen RB; Gambetti P
Ann Neurol; 1996 Jun; 39(6):767-78. PubMed ID: 8651649
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
Schmitz M; Lüllmann K; Zafar S; Ebert E; Wohlhage M; Oikonomou P; Schlomm M; Mitrova E; Beekes M; Zerr I
Neurobiol Aging; 2014 May; 35(5):1177-88. PubMed ID: 24360565
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. First participant diagnosed with Creutzfeldt-Jakob disease in the population-based Rotterdam Study was classified with mild cognitive impairment.
Karamujić-Čomić H; Rozemuller AJM; Ikram MA; van Duijn CM
BMJ Case Rep; 2021 Mar; 14(3):. PubMed ID: 33782059
[TBL] [Abstract][Full Text] [Related]
12. Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development.
Mitrová E; Belay G
Acta Virol; 2002; 46(1):31-9. PubMed ID: 12197632
[TBL] [Abstract][Full Text] [Related]
13. Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease.
Shibuya S; Higuchi J; Shin RW; Tateishi J; Kitamoto T
Ann Neurol; 1998 Jun; 43(6):826-8. PubMed ID: 9629853
[TBL] [Abstract][Full Text] [Related]
14. Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease.
Worrall BB; Herman ST; Capellari S; Lynch T; Chin S; Gambetti P; Parchi P
J Neurol Neurosurg Psychiatry; 1999 Nov; 67(5):671-4. PubMed ID: 10519879
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Absence of association between codon 129 and 219 polymorphisms of the prion protein gene and vascular dementia.
Jeong BH; Na HR; Bae JC; Lee KH; Lee YJ; Kim NH; Song JH; Carp RI; Kim YS
Dement Geriatr Cogn Disord; 2007; 24(2):86-90. PubMed ID: 17570906
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Clinicopathological phenotype of codon 129 valine homozygote sporadic Creutzfeldt-Jakob disease.
Kovacs GG; Head MW; Bunn T; Laszlo L; Will RG; Ironside JW
Neuropathol Appl Neurobiol; 2000 Oct; 26(5):463-72. PubMed ID: 11054187
[TBL] [Abstract][Full Text] [Related]
19. The influence of PRNP polymorphisms on human prion disease susceptibility: an update.
Kobayashi A; Teruya K; Matsuura Y; Shirai T; Nakamura Y; Yamada M; Mizusawa H; Mohri S; Kitamoto T
Acta Neuropathol; 2015 Aug; 130(2):159-70. PubMed ID: 26022925
[TBL] [Abstract][Full Text] [Related]
20. Polymorphism of PRNP codons in the normal Icelandic population.
Georgsson G; Tryggvason T; Jonasdottir AD; Gudmundsson S; Thorgeirsdottir S
Acta Neurol Scand; 2006 Jun; 113(6):419-25. PubMed ID: 16674609
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]