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Items: 17

1.

A Positive Control for Detection of Functional CD4 T Cells in PBMC: The CPI Pool.

Schiller A, Zhang T, Li R, Duechting A, Sundararaman S, Przybyla A, Kuerten S, Lehmann PV.

Cells. 2017 Dec 7;6(4). pii: E47. doi: 10.3390/cells6040047.

2.

An aggregation-specific enzyme-linked immunosorbent assay: detection of conformational differences between recombinant PrP protein dimers and PrP(Sc) aggregates.

Pan T, Chang B, Wong P, Li C, Li R, Kang SC, Robinson JD, Thompsett AR, Tein P, Yin S, Barnard G, McConnell I, Brown DR, Wisniewski T, Sy MS.

J Virol. 2005 Oct;79(19):12355-64.

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Biochemical fingerprints of prion diseases: scrapie prion protein in human prion diseases that share prion genotype and type.

Pan T, Li R, Kang SC, Pastore M, Wong BS, Ironside J, Gambetti P, Sy MS.

J Neurochem. 2005 Jan;92(1):132-42.

6.

Protease-resistant human prion protein and ferritin are cotransported across Caco-2 epithelial cells: implications for species barrier in prion uptake from the intestine.

Mishra RS, Basu S, Gu Y, Luo X, Zou WQ, Mishra R, Li R, Chen SG, Gambetti P, Fujioka H, Singh N.

J Neurosci. 2004 Dec 15;24(50):11280-90.

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Prion protein is ubiquitinated after developing protease resistance in the brains of scrapie-infected mice.

Kang SC, Brown DR, Whiteman M, Li R, Pan T, Perry G, Wisniewski T, Sy MS, Wong BS.

J Pathol. 2004 May;203(1):603-8.

PMID:
15095484
9.

Mapping the functional domain of the prion protein.

Cui T, Daniels M, Wong BS, Li R, Sy MS, Sassoon J, Brown DR.

Eur J Biochem. 2003 Aug;270(16):3368-76.

10.

On the same cell type GPI-anchored normal cellular prion and DAF protein exhibit different biological properties.

Li R, Liu T, Yoshihiro F, Tary-Lehmann M, Obrenovich M, Kuekrek H, Kang SC, Pan T, Wong BS, Medof ME, Sy MS.

Biochem Biophys Res Commun. 2003 Apr 4;303(2):446-51.

PMID:
12659837
11.

Guanidine hydrochloride extraction and detection of prion proteins in mouse and hamster prion diseases by ELISA.

Kang SC, Li R, Wang C, Pan T, Liu T, Rubenstein R, Barnard G, Wong BS, Sy MS.

J Pathol. 2003 Apr;199(4):534-41.

PMID:
12635145
12.

Aggresome formation by mutant prion proteins: the unfolding role of proteasomes in familial prion disorders.

Mishra RS, Bose S, Gu Y, Li R, Singh N.

J Alzheimers Dis. 2003 Feb;5(1):15-23.

PMID:
12590162
13.

Anti-prion antibodies for prophylaxis following prion exposure in mice.

Sigurdsson EM, Sy MS, Li R, Scholtzova H, Kascsak RJ, Kascsak R, Carp R, Meeker HC, Frangione B, Wisniewski T.

Neurosci Lett. 2003 Jan 23;336(3):185-7.

PMID:
12505623
14.

Intercellular transfer of the cellular prion protein.

Liu T, Li R, Pan T, Liu D, Petersen RB, Wong BS, Gambetti P, Sy MS.

J Biol Chem. 2002 Dec 6;277(49):47671-8. Epub 2002 Sep 30.

15.

Cell-surface prion protein interacts with glycosaminoglycans.

Pan T, Wong BS, Liu T, Li R, Petersen RB, Sy MS.

Biochem J. 2002 Nov 15;368(Pt 1):81-90.

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Prion peptide 106-126 modulates the aggregation of cellular prion protein and induces the synthesis of potentially neurotoxic transmembrane PrP.

Gu Y, Fujioka H, Mishra RS, Li R, Singh N.

J Biol Chem. 2002 Jan 18;277(3):2275-86. Epub 2001 Oct 26.

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