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Items: 1 to 20 of 208

1.

Variation of the prion gene in chimpanzees and its implication for prion diseases.

Soldevila M, Andrés AM, Blancher A, Calafell F, Ordoñez M, Pumarola M, Oliva B, Aramburu J, Bertranpetit J.

Neurosci Lett. 2004 Jan 30;355(3):157-60.

PMID:
14732455
2.
3.

[Molecular basis of familial and sporadic forms of human prion diseases].

Laplanche JL.

Transfus Clin Biol. 1994;1(5):345-53. French.

PMID:
7812461
4.

[Genetic background of human prion diseases].

Kovács GG.

Ideggyogy Sz. 2007 Nov 30;60(11-12):438-46. Review. Hungarian.

PMID:
18198790
5.

Molecular approaches to mechanisms of prion diseases.

Bratosiewicz-Wasik J, Wasik TJ, Liberski PP.

Folia Neuropathol. 2004;42 Suppl A:33-46. Review.

PMID:
15449458
6.

Analysis of the prion protein in primates reveals a new polymorphism in codon 226 (Y226F).

Glatzel M, Pekarik V, Lührs T, Dittami J, Aguzzi A.

Biol Chem. 2002 Jun;383(6):1021-5.

PMID:
12222676
7.

Codon 219 in Creutzfeldt-Jakob disease in Poland.

Bratosiewicz-Wasik J, Wasik TJ, Liberski PP.

Acta Neurobiol Exp (Wars). 2002;62(3):149-51.

8.

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.

PMID:
16674609
9.

Mutations of the prion protein gene phenotypic spectrum.

Kovács GG, Trabattoni G, Hainfellner JA, Ironside JW, Knight RS, Budka H.

J Neurol. 2002 Nov;249(11):1567-82.

PMID:
12420099
10.
11.

Prion gene sequence variation within diverse groups of U.S. sheep, beef cattle, and deer.

Heaton MP, Leymaster KA, Freking BA, Hawk DA, Smith TP, Keele JW, Snelling WM, Fox JM, Chitko-McKown CG, Laegreid WW.

Mamm Genome. 2003 Nov;14(11):765-77.

PMID:
14722726
12.

Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation.

Chapman J, Arlazoroff A, Goldfarb LG, Cervenakova L, Neufeld MY, Werber E, Herbert M, Brown P, Gajdusek DC, Korczyn AD.

Neurology. 1996 Mar;46(3):758-61.

PMID:
8618678
13.

Infectious amyloid precursor gene sequences in primates used for experimental transmission of human spongiform encephalopathy.

Cervenáková L, Brown P, Goldfarb LG, Nagle J, Pettrone K, Rubenstein R, Dubnick M, Gibbs CJ Jr, Gajdusek DC.

Proc Natl Acad Sci U S A. 1994 Dec 6;91(25):12159-62. Erratum in: Proc Natl Acad Sci U S A 1995 Apr 11;92(8):3631.

14.

Upstream AUGs modulate prion protein translation in vitro.

Schröder B, Nickodemus R, Jürgens T, Bodemer W.

Acta Virol. 2002;46(3):159-67.

PMID:
12580378
15.

Functional and structural differences between the prion protein from two alleles prnp(a) and prnp(b) of mouse.

Brown DR, Iordanova IK, Wong BS, Vénien-Bryan C, Hafiz F, Glasssmith LL, Sy MS, Gambetti P, Jones IM, Clive C, Haswell SJ.

Eur J Biochem. 2000 Apr;267(8):2452-9. Erratum in: Eur J Biochem 2000 Jun;267(12):3915.

16.

Genetic prion disease: the EUROCJD experience.

Kovács GG, Puopolo M, Ladogana A, Pocchiari M, Budka H, van Duijn C, Collins SJ, Boyd A, Giulivi A, Coulthart M, Delasnerie-Laupretre N, Brandel JP, Zerr I, Kretzschmar HA, de Pedro-Cuesta J, Calero-Lara M, Glatzel M, Aguzzi A, Bishop M, Knight R, Belay G, Will R, Mitrova E; EUROCJD.

Hum Genet. 2005 Nov;118(2):166-74. Epub 2005 Nov 15.

PMID:
16187142
17.

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
18.
19.

Molecular genetics of human prion diseases in Germany.

Windl O, Giese A, Schulz-Schaeffer W, Zerr I, Skworc K, Arendt S, Oberdieck C, Bodemer M, Poser S, Kretzschmar HA.

Hum Genet. 1999 Sep;105(3):244-52.

PMID:
10987652
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