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Results: 1 to 20 of 103

Similar articles for PubMed (Select 15488240)

1.

High capacity and low cost detection of prion protein gene variant alleles by denaturing HPLC.

Castro RM, Landemberger MC, Walz R, Carlotti CG Jr, Huang N, Cunha DR, Moura R, Caballero OL, Sakamoto AC, Nitrini R, Brentani RR, Martins VR.

J Neurosci Methods. 2004 Oct 30;139(2):263-9.

PMID:
15488240
2.

Cognitive performance of patients with mesial temporal lobe epilepsy is not associated with human prion protein gene variant allele at codons 129 and 171.

Coimbra ER, Rezek K, Escorsi-Rosset S, Landemberger MC, Castro RM, Valadão MN, Guarnieri R, Velasco TR, Terra-Bustamante VC, Bianchin MM, Wichert-Ana L, Alexandre V Jr, Brentani RR, Martins VR, Sakamoto AC, Walz R.

Epilepsy Behav. 2006 May;8(3):635-42. Epub 2006 Apr 3. Erratum in: Epilepsy Behav. 2008 Jan;12(1):210-3.

PMID:
16580884
3.

Surgical outcome in mesial temporal sclerosis correlates with prion protein gene variant.

Walz R, Castro RM, Velasco TR, Alexandre V Jr, Lopes MH, Leite JP, Santos AC, Assirati JA Jr, Wichert-Ana L, Terra-Bustamante VC, Bianchin MM, Maciag PC, Ribeiro KB, Guarnieri R, Araújo D, Cabalero O, Moura R, Salim AC, Kindlmann K, Landemberger MC, Marques W Jr, Fernandes RM, Serafini LN, Machado HR, Carlotti CG Jr, Brentani RR, Sakamoto AC, Martins VR.

Neurology. 2003 Nov 11;61(9):1204-10.

PMID:
14610121
4.

A processed pseudogene contributes to apparent mule deer prion gene heterogeneity.

Brayton KA, O'Rourke KI, Lyda AK, Miller MW, Knowles DP.

Gene. 2004 Feb 4;326:167-73.

PMID:
14729275
5.

A rapid and efficient method for the detection of point mutations of the human prion protein gene (PRNP) by direct sequencing.

Petraroli R, Vaccari G, Pocchiari M.

J Neurosci Methods. 2000 Jun 30;99(1-2):59-63.

PMID:
10936643
6.

Single nucleotide polymorphisms of the prion protein gene (PRNP) in Chinese pig breeds.

Meng L, Zhao D, Liu H, Yang J, Ning Z.

Xenotransplantation. 2005 Jul;12(4):324-6.

PMID:
15943782
7.

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):319-24. Epub 2004 May 18.

PMID:
15148589
8.

High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC).

Wolford JK, Blunt D, Ballecer C, Prochazka M.

Hum Genet. 2000 Nov;107(5):483-7.

PMID:
11140946
9.

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. Epub 2005 Oct 11.

PMID:
16217673
10.

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 21;421(1):1-4. Epub 2006 Nov 7.

PMID:
17092648
11.

Bovine prion protein gene (PRNP) promoter polymorphisms modulate PRNP expression and may be responsible for differences in bovine spongiform encephalopathy susceptibility.

Sander P, Hamann H, Drögemüller C, Kashkevich K, Schiebel K, Leeb T.

J Biol Chem. 2005 Nov 11;280(45):37408-14. Epub 2005 Sep 1.

12.

The M129V polymorphism of codon 129 in the prion gene (PRNP) in the Danish population.

Dyrbye H, Broholm H, Dziegiel MH, Laursen H.

Eur J Epidemiol. 2008;23(1):23-7. Epub 2007 Nov 7.

PMID:
17987393
13.

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. Epub 2007 Jun 14.

PMID:
17570906
14.

Prnp gene and cerebellum volume in patients with refractory mesial temporal lobe epilepsy.

Valadão MN, Coimbra ER, Landemberger MC, Velasco TR, Terra VC, Wichert-Ana L, Alexandre V Jr, Araújo D Jr, Guarnieri R, Martins VR, Santos AC, Sakamoto AC, Walz R.

Neurol Sci. 2014 Feb;35(2):239-44. doi: 10.1007/s10072-013-1494-6. Epub 2013 Oct 5.

PMID:
24091711
15.

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.

PMID:
17539938
16.

Prion gene haplotypes of U.S. cattle.

Clawson ML, Heaton MP, Keele JW, Smith TP, Harhay GP, Laegreid WW.

BMC Genet. 2006 Nov 8;7:51.

17.

A simple and rapid method for sequencing the entire coding region of the human prion protein (PrP) gene.

Boussin F, Jaegly A, Deslys JP, Dormont D.

J Neurosci Methods. 1994 Sep;54(1):103-7.

PMID:
7815814
18.

First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases.

Peoc'h K, Guérin C, Brandel JP, Launay JM, Laplanche JL.

Neurosci Lett. 2000 Jun 2;286(2):144-8.

PMID:
10825657
19.

Polymorphisms of the prion protein gene (PRNP) in Hanwoo (Bos taurus coreanae) and Holstein cattle.

Jeong BH, Sohn HJ, Lee JO, Kim NH, Kim JI, Lee SY, Cho IS, Joo YS, Carp RI, Kim YS.

Genes Genet Syst. 2005 Aug;80(4):303-8.

20.

Rapid and accurate detection of atypical and Kalow variants in the butyrylcholinesterase gene using denaturing high performance liquid chromatography.

Levano S, Keller D, Schobinger E, Urwyler A, Girard T.

Anesth Analg. 2008 Jan;106(1):147-51, table of contents. doi: 10.1213/01.ane.0000296455.31211.bd.

PMID:
18165570
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