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Results: 1 to 20 of 113

1.

Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease.

Kovacs GG, Sanchez-Juan P, Ströbel T, Schuur M, Poleggi A, Nocentini S, Giannattasio C, Belay G, Bishop M, Capellari S, Parchi P, Gelpi E, Gal A, Bakos A, Molnar MJ, Heinemann U, Zerr I, Knight RS, Mitrova E, van Duijn C, Budka H.

Alzheimer Dis Assoc Disord. 2010 Jan-Mar;24(1):104-7. doi: 10.1097/WAD.0b013e3181ad378c.

PMID:
19571726
[PubMed - indexed for MEDLINE]
2.

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. doi: 10.1159/000246343. Epub 2009 Oct 13.

PMID:
19828951
[PubMed - indexed for MEDLINE]
3.

Genetic associations between cathepsin D exon 2 C-->T polymorphism and Alzheimer's disease, and pathological correlations with genotype.

Davidson Y, Gibbons L, Pritchard A, Hardicre J, Wren J, Tian J, Shi J, Stopford C, Julien C, Thompson J, Payton A, Thaker U, Hayes AJ, Iwatsubo T, Pickering-Brown SM, Pendleton N, Horan MA, Burns A, Purandare N, Lendon CL, Neary D, Snowden JS, Mann DM.

J Neurol Neurosurg Psychiatry. 2006 Apr;77(4):515-7.

PMID:
16543533
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

[The C224T polymorphism in the cathepsin D gene is not associated with sporadic Alzheimer's disease in Chinese].

Sun Y, Shi JJ, Zhang SZ, Tang MN, Han HY, Guo YB, Ma C, Liu XH, Li T.

Yi Chuan. 2005 Mar;27(2):190-4. Chinese.

PMID:
15843343
[PubMed - indexed for MEDLINE]
5.

Cathepsin D SNP associated with increased risk of variant Creutzfeldt-Jakob disease.

Bishop MT, Kovacs GG, Sanchez-Juan P, Knight RS.

BMC Med Genet. 2008 Apr 21;9:31. doi: 10.1186/1471-2350-9-31.

PMID:
18426579
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

The cathepsin D gene exon 2 (C224T) polymorphism and sporadic Alzheimer's disease in European populations.

Capurso C, Solfrizzi V, D'Introno A, Colacicco AM, Capurso SA, Mastroianni F, Liaci M, Vendemiale G, Capurso A, Panza F.

J Gerontol A Biol Sci Med Sci. 2005 Aug;60(8):991-6.

PMID:
16127101
[PubMed - indexed for MEDLINE]
7.

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):311-4. Epub 2005 Jun 3.

PMID:
15933804
[PubMed - indexed for MEDLINE]
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. doi: 10.1111/j.1468-1331.2008.02203.x. Epub 2008 Jun 28.

PMID:
18549395
[PubMed - indexed for MEDLINE]
9.

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.

PMID:
14970845
[PubMed - indexed for MEDLINE]
Free Article
10.

Modulation of disease risk according to a cathepsin D / apolipoprotein E genotype in Parkinson's disease.

Schulte T, Böhringer S, Schöls L, Müller T, Fischer C, Riess O, Przuntek H, Berger K, Epplen JT, Krüger R.

J Neural Transm. 2003 Jul;110(7):749-55.

PMID:
12811635
[PubMed - indexed for MEDLINE]
11.

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.

PMID:
15986038
[PubMed - indexed for MEDLINE]
Free Article
12.

Variation at the ADAM10 gene locus is not associated with Creutzfeldt-Jakob disease.

Plamont MA, Chasseigneaux S, Delasnerie-Lauprêtre N, Beaudry P, Peoc'h K, Laplanche JL.

Neurosci Lett. 2003 Jun 26;344(2):132-4.

PMID:
12782344
[PubMed - indexed for MEDLINE]
13.

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 16;411(3):163-7. Epub 2006 Nov 28.

PMID:
17134829
[PubMed - indexed for MEDLINE]
14.

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. Epub 2001 Nov 5.

PMID:
11704923
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

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 13;12:108. doi: 10.1186/1471-2350-12-108.

PMID:
21838916
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Genetic polymorphism in exon 2 of cathepsin D is not associated with vascular dementia.

Jeong BH, Lee KH, Lee YJ, Yun J, Park YJ, Kim YH, Cho YS, Choi EK, Carp RI, Kim YS.

Acta Neurol Scand. 2011 Jun;123(6):419-23. doi: 10.1111/j.1600-0404.2010.01400.x.

PMID:
20597865
[PubMed - indexed for MEDLINE]
17.

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. doi: 10.1007/s11033-012-1954-8. Epub 2012 Oct 11.

PMID:
23053962
[PubMed - indexed for MEDLINE]
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. Erratum in: Hum Genet 1995 May;95(5):605.

PMID:
7927332
[PubMed - indexed for MEDLINE]
19.

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 29;343(1306):385-90.

PMID:
7913755
[PubMed - indexed for MEDLINE]
20.

Alpha1 antichymotrypsin signal peptide polymorphism in sporadic Creutzfeldt-Jakob disease.

Salvatore M, Seeber AC, Nacmias B, Petraroli R, Sorbi S, Pocchiari M.

Neurosci Lett. 1997 May 16;227(2):140-2.

PMID:
9180223
[PubMed - indexed for MEDLINE]

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