Chen SG - Search Results

1

Expression and structural characterization of the recombinant human doppel protein.

Lu K, Wang W, Xie Z, Wong BS, Li R, Petersen RB, Sy MS, Chen SG. Lu K, et al. Among authors: chen sg. Biochemistry. 2000 Nov 7;39(44):13575-83. doi: 10.1021/bi001523m. Biochemistry. 2000. PMID: 11063595

2

Induction of HO-1 and NOS in doppel-expressing mice devoid of PrP: implications for doppel function.

Wong BS, Liu T, Paisley D, Li R, Pan T, Chen SG, Perry G, Petersen RB, Smith MA, Melton DW, Gambetti P, Brown DR, Sy MS. Wong BS, et al. Among authors: chen sg. Mol Cell Neurosci. 2001 Apr;17(4):768-75. doi: 10.1006/mcne.2001.0963. Mol Cell Neurosci. 2001. PMID: 11312611

3

Absence of protease-resistant prion protein in the cerebrospinal fluid of Creutzfeldt-Jakob disease.

Wong BS, Green AJ, Li R, Xie Z, Pan T, Liu T, Chen SG, Gambetti P, Sy MS. Wong BS, et al. Among authors: chen sg. J Pathol. 2001 May;194(1):9-14. doi: 10.1002/path.872. J Pathol. 2001. PMID: 11329135

4

Aberrant metal binding by prion protein in human prion disease.

Wong BS, Chen SG, Colucci M, Xie Z, Pan T, Liu T, Li R, Gambetti P, Sy MS, Brown DR. Wong BS, et al. Among authors: chen sg. J Neurochem. 2001 Sep;78(6):1400-8. doi: 10.1046/j.1471-4159.2001.00522.x. J Neurochem. 2001. PMID: 11579148 Free article.

5

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.

Gambetti P, Parchi P, Petersen RB, Chen SG, Lugaresi E. Gambetti P, et al. Among authors: chen sg. Brain Pathol. 1995 Jan;5(1):43-51. doi: 10.1111/j.1750-3639.1995.tb00576.x. Brain Pathol. 1995. PMID: 7767490 Review.

6

Prion protein aggregation reverted by low temperature in transfected cells carrying a prion protein gene mutation.

Singh N, Zanusso G, Chen SG, Fujioka H, Richardson S, Gambetti P, Petersen RB. Singh N, et al. Among authors: chen sg. J Biol Chem. 1997 Nov 7;272(45):28461-70. doi: 10.1074/jbc.272.45.28461. J Biol Chem. 1997. PMID: 9353306 Free article.

7

Aggregation and fibrillization of the recombinant human prion protein huPrP90-231.

Swietnicki W, Morillas M, Chen SG, Gambetti P, Surewicz WK. Swietnicki W, et al. Among authors: chen sg. Biochemistry. 2000 Jan 18;39(2):424-31. doi: 10.1021/bi991967m. Biochemistry. 2000. PMID: 10631004

8

Genetic influence on the structural variations of the abnormal prion protein.

Parchi P, Zou W, Wang W, Brown P, Capellari S, Ghetti B, Kopp N, Schulz-Schaeffer WJ, Kretzschmar HA, Head MW, Ironside JW, Gambetti P, Chen SG. Parchi P, et al. Among authors: chen sg. Proc Natl Acad Sci U S A. 2000 Aug 29;97(18):10168-72. doi: 10.1073/pnas.97.18.10168. Proc Natl Acad Sci U S A. 2000. PMID: 10963679 Free PMC article.

9

Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17.

Petersen RB, Tabaton M, Chen SG, Monari L, Richardson SL, Lynch T, Manetto V, Lanska DJ, Markesbery WR, Lynches T [corrected to Lynch T], et al. Petersen RB, et al. Among authors: chen sg. Neurology. 1995 Jun;45(6):1062-7. doi: 10.1212/wnl.45.6.1062. Neurology. 1995. PMID: 7783864

10

Molecular pathology of fatal familial insomnia.

Parchi P, Petersen RB, Chen SG, Autilio-Gambetti L, Capellari S, Monari L, Cortelli P, Montagna P, Lugaresi E, Gambetti P. Parchi P, et al. Among authors: chen sg. Brain Pathol. 1998 Jul;8(3):539-48. doi: 10.1111/j.1750-3639.1998.tb00176.x. Brain Pathol. 1998. PMID: 9669705 Free PMC article. Review.

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