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Results: 1 to 20 of 43

1.

ZBTB1 is a determinant of lymphoid development.

Siggs OM, Li X, Xia Y, Beutler B.

J Exp Med. 2012 Jan 16;209(1):19-27. doi: 10.1084/jem.20112084. Epub 2011 Dec 26.

PMID:
22201126
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Copper(II)-induced secondary structure changes and reduced folding stability of the prion protein.

Younan ND, Klewpatinond M, Davies P, Ruban AV, Brown DR, Viles JH.

J Mol Biol. 2011 Jul 15;410(3):369-82. doi: 10.1016/j.jmb.2011.05.013. Epub 2011 May 17.

PMID:
21619885
[PubMed - indexed for MEDLINE]
3.

Variably protease-sensitive prionopathy: a novel disease of the prion protein.

Gambetti P, Puoti G, Zou WQ.

J Mol Neurosci. 2011 Nov;45(3):422-4. doi: 10.1007/s12031-011-9543-1. Epub 2011 May 17.

PMID:
21584652
[PubMed - indexed for MEDLINE]
4.

ATP7A-related copper transport diseases-emerging concepts and future trends.

Kaler SG.

Nat Rev Neurol. 2011 Jan;7(1):15-29. doi: 10.1038/nrneurol.2010.180. Review.

PMID:
21221114
[PubMed - indexed for MEDLINE]
5.

Mice with altered serotonin 2C receptor RNA editing display characteristics of Prader-Willi syndrome.

Morabito MV, Abbas AI, Hood JL, Kesterson RA, Jacobs MM, Kump DS, Hachey DL, Roth BL, Emeson RB.

Neurobiol Dis. 2010 Aug;39(2):169-80. doi: 10.1016/j.nbd.2010.04.004. Epub 2010 Apr 13.

PMID:
20394819
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

A method and server for predicting damaging missense mutations.

Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, Kondrashov AS, Sunyaev SR.

Nat Methods. 2010 Apr;7(4):248-9. doi: 10.1038/nmeth0410-248. No abstract available.

PMID:
20354512
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy.

Kennerson ML, Nicholson GA, Kaler SG, Kowalski B, Mercer JF, Tang J, Llanos RM, Chu S, Takata RI, Speck-Martins CE, Baets J, Almeida-Souza L, Fischer D, Timmerman V, Taylor PE, Scherer SS, Ferguson TA, Bird TD, De Jonghe P, Feely SM, Shy ME, Garbern JY.

Am J Hum Genet. 2010 Mar 12;86(3):343-52. doi: 10.1016/j.ajhg.2010.01.027. Epub 2010 Feb 18.

PMID:
20170900
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Role of copper and manganese in prion disease progression.

Mitteregger G, Korte S, Shakarami M, Herms J, Kretzschmar HA.

Brain Res. 2009 Oct 6;1292:155-64. doi: 10.1016/j.brainres.2009.07.051. Epub 2009 Jul 25.

PMID:
19635464
[PubMed - indexed for MEDLINE]
9.

Early onset prion disease from octarepeat expansion correlates with copper binding properties.

Stevens DJ, Walter ED, Rodríguez A, Draper D, Davies P, Brown DR, Millhauser GL.

PLoS Pathog. 2009 Apr;5(4):e1000390. doi: 10.1371/journal.ppat.1000390. Epub 2009 Apr 17.

PMID:
19381258
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

ENU mutagenesis in mice.

Georgel P, Du X, Hoebe K, Beutler B.

Methods Mol Biol. 2008;415:1-16. doi: 10.1007/978-1-59745-570-1_1.

PMID:
18370145
[PubMed - indexed for MEDLINE]
11.

Copper(II) ion binding to cellular prion protein.

Zidar J, Pirc ET, Hodoscek M, Bukovec P.

J Chem Inf Model. 2008 Feb;48(2):283-7. doi: 10.1021/ci700226c. Epub 2008 Feb 2.

PMID:
18247504
[PubMed - indexed for MEDLINE]
12.

Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes.

de Bie P, Muller P, Wijmenga C, Klomp LW.

J Med Genet. 2007 Nov;44(11):673-88. Epub 2007 Aug 23. Review.

PMID:
17717039
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Isolation and characterization of a proteinase K-sensitive PrPSc fraction.

Pastrana MA, Sajnani G, Onisko B, Castilla J, Morales R, Soto C, Requena JR.

Biochemistry. 2006 Dec 26;45(51):15710-7. Epub 2006 Dec 6.

PMID:
17176093
[PubMed - indexed for MEDLINE]
14.

Proteinase K-sensitive disease-associated ovine prion protein revealed by conformation-dependent immunoassay.

Thackray AM, Hopkins L, Bujdoso R.

Biochem J. 2007 Jan 15;401(2):475-83.

PMID:
17018021
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Copper (II) ions potently inhibit purified PrPres amplification.

Orem NR, Geoghegan JC, Deleault NR, Kascsak R, Supattapone S.

J Neurochem. 2006 Mar;96(5):1409-15. Epub 2006 Jan 17.

PMID:
16417569
[PubMed - indexed for MEDLINE]
16.

Induction of cellular prion protein gene expression by copper in neurons.

Varela-Nallar L, Toledo EM, Larrondo LF, Cabral AL, Martins VR, Inestrosa NC.

Am J Physiol Cell Physiol. 2006 Jan;290(1):C271-81. Epub 2005 Sep 7.

PMID:
16148034
[PubMed - indexed for MEDLINE]
Free Article
17.

Gene expression profiling in chronic copper overload reveals upregulation of Prnp and App.

Armendariz AD, Gonzalez M, Loguinov AV, Vulpe CD.

Physiol Genomics. 2004 Dec 15;20(1):45-54. Epub 2004 Oct 5.

PMID:
15467011
[PubMed - indexed for MEDLINE]
Free Article
18.

Cellular prion protein acquires resistance to proteolytic degradation following copper ion binding.

Kuczius T, Buschmann A, Zhang W, Karch H, Becker K, Peters G, Groschup MH.

Biol Chem. 2004 Aug;385(8):739-47.

PMID:
15449710
[PubMed - indexed for MEDLINE]
19.

Preferential Cu2+ coordination by His96 and His111 induces beta-sheet formation in the unstructured amyloidogenic region of the prion protein.

Jones CE, Abdelraheim SR, Brown DR, Viles JH.

J Biol Chem. 2004 Jul 30;279(31):32018-27. Epub 2004 May 15.

PMID:
15145944
[PubMed - indexed for MEDLINE]
Free Article
20.

Biology, structure and mechanism of P-type ATPases.

Kühlbrandt W.

Nat Rev Mol Cell Biol. 2004 Apr;5(4):282-95. Review. No abstract available.

PMID:
15071553
[PubMed - indexed for MEDLINE]

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