| Year |
Citation |
Score |
| 2021 |
Wang Q, Davis PB, Qi X, Chen SG, Gurney ME, Perry G, Doraiswamy PM, Xu R. Gut-microbiota-microglia-brain interactions in Alzheimer's disease: knowledge-based, multi-dimensional characterization. Alzheimer's Research & Therapy. 13: 177. PMID 34670619 DOI: 10.1186/s13195-021-00917-1 |
0.378 |
|
| 2021 |
Zheng C, Fillmore NR, Ramos-Cejudo J, Brophy M, Osorio R, Gurney ME, Qiu WQ, Au R, Perry G, Dubreuil M, Chen SG, Qi X, Davis PB, Do N, Xu R. Potential long-term effect of tumor necrosis factor inhibitors on dementia risk: A propensity score matched retrospective cohort study in US veterans. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 34569707 DOI: 10.1002/alz.12465 |
0.3 |
|
| 2019 |
Schaffner A, Li X, Gomez-Llorente Y, Leandrou E, Memou A, Clemente N, Yao C, Afsari F, Zhi L, Pan N, Morohashi K, Hua X, Zhou MM, Wang C, Zhang H, ... Chen SG, et al. Vitamin B modulates Parkinson's disease LRRK2 kinase activity through allosteric regulation and confers neuroprotection. Cell Research. PMID 30858560 DOI: 10.1038/S41422-019-0153-8 |
0.497 |
|
| 2018 |
Yan T, Wang L, Gao J, Siedlak SL, Huntley ML, Termsarasab P, Perry G, Chen SG, Wang X. Rab10 Phosphorylation is a Prominent Pathological Feature in Alzheimer's Disease. Journal of Alzheimer's Disease : Jad. PMID 29562525 DOI: 10.3233/Jad-180023 |
0.462 |
|
| 2017 |
Cracco L, Notari S, Cali I, Sy MS, Chen SG, Cohen ML, Ghetti B, Appleby BS, Zou WQ, Caughey B, Safar JG, Gambetti P. Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type. Scientific Reports. 7: 38280. PMID 28091514 DOI: 10.1038/Srep38280 |
0.629 |
|
| 2016 |
Chen SG, Stribinskis V, Rane MJ, Demuth DR, Gozal E, Roberts AM, Jagadapillai R, Liu R, Choe K, Shivakumar B, Son F, Jin S, Kerber R, Adame A, Masliah E, et al. Exposure to the Functional Bacterial Amyloid Protein Curli Enhances Alpha-Synuclein Aggregation in Aged Fischer 344 Rats and Caenorhabditis elegans. Scientific Reports. 6: 34477. PMID 27708338 DOI: 10.1038/Srep34477 |
0.323 |
|
| 2016 |
Johnson WM, Golczak M, Choe K, Currran PL, Gorelenkova Miller O, Yao C, Wang W, Lin J, Milkovic NM, Ray A, Ravindranath V, Zhu X, Wilson MA, Wilson-Delfosse AL, Chen SG, et al. Regulation of DJ-1 by glutaredoxin 1 in vivo - implications for Parkinson's disease. Biochemistry. PMID 26894491 DOI: 10.1021/Acs.Biochem.5B01132 |
0.527 |
|
| 2015 |
Johnson WM, Wilson-Delfosse AL, Chen SG, Mieyal JJ. The roles of redox enzymes in Parkinson's disease: Focus on glutaredoxin. Therapeutic Targets For Neurological Diseases. 2. PMID 26097894 DOI: 10.14800/Ttnd.790 |
0.307 |
|
| 2015 |
Safar JG, Xiao X, Kabir ME, Chen S, Kim C, Haldiman T, Cohen Y, Chen W, Cohen ML, Surewicz WK. Structural determinants of phenotypic diversity and replication rate of human prions. Plos Pathogens. 11: e1004832. PMID 25875953 DOI: 10.1371/Journal.Ppat.1004832 |
0.318 |
|
| 2015 |
Johnson WM, Yao C, Siedlak SL, Wang W, Zhu X, Caldwell GA, Wilson-Delfosse AL, Mieyal JJ, Chen SG. Glutaredoxin deficiency exacerbates neurodegeneration in C. elegans models of Parkinson's disease. Human Molecular Genetics. 24: 1322-35. PMID 25355420 DOI: 10.1093/Hmg/Ddu542 |
0.475 |
|
| 2013 |
Yao C, Johnson WM, Gao Y, Wang W, Zhang J, Deak M, Alessi DR, Zhu X, Mieyal JJ, Roder H, Wilson-Delfosse AL, Chen SG. Kinase inhibitors arrest neurodegeneration in cell and C. elegans models of LRRK2 toxicity. Human Molecular Genetics. 22: 328-44. PMID 23065705 DOI: 10.1093/Hmg/Dds431 |
0.481 |
|
| 2012 |
Notari S, Qing L, Pocchiari M, Dagdanova A, Hatcher K, Dogterom A, Groisman JF, Lumholtz IB, Puopolo M, Lasmezas C, Chen SG, Kong Q, Gambetti P. Assessing prion infectivity of human urine in sporadic Creutzfeldt-Jakob disease. Emerging Infectious Diseases. 18: 21-8. PMID 22260924 DOI: 10.3201/Eid1801.110589 |
0.599 |
|
| 2012 |
Wang X, Yan MH, Fujioka H, Liu J, Wilson-Delfosse A, Chen SG, Perry G, Casadesus G, Zhu X. LRRK2 regulates mitochondrial dynamics and function through direct interaction with DLP1. Human Molecular Genetics. 21: 1931-44. PMID 22228096 DOI: 10.1093/Hmg/Dds003 |
0.435 |
|
| 2012 |
Perry G, Yan M, Fujioka H, Wilson-Delfosse A, Chen S, Casadesus G, Zhu X, Wang X, Liu J. LRRK2 Directly Interacts with DLP1 to Regulate Mitochondrial Dynamics and Function Microscopy and Microanalysis. 18: 196-197. DOI: 10.1017/S1431927612002838 |
0.366 |
|
| 2011 |
Wang P, Hatcher KL, Bartz JC, Chen SG, Skinner P, Richt J, Liu H, Sreevatsan S. Selection and characterization of DNA aptamers against PrP(Sc). Experimental Biology and Medicine (Maywood, N.J.). 236: 466-76. PMID 21444369 DOI: 10.1258/Ebm.2011.010323 |
0.349 |
|
| 2011 |
Castellani RJ, Nugent SL, Morrison AL, Zhu X, Lee HG, Harris PL, Bajić V, Sharma HS, Chen SG, Oettgen P, Perry G, Smith MA. CD3 in Lewy pathology: does the abnormal recall of neurodevelopmental processes underlie Parkinson's disease. Journal of Neural Transmission (Vienna, Austria : 1996). 118: 23-6. PMID 20972807 DOI: 10.1007/S00702-010-0485-5 |
0.54 |
|
| 2010 |
Dagdanova A, Ilchenko S, Notari S, Yang Q, Obrenovich ME, Hatcher K, McAnulty P, Huang L, Zou W, Kong Q, Gambetti P, Chen SG. Characterization of the prion protein in human urine. The Journal of Biological Chemistry. 285: 30489-95. PMID 20670940 DOI: 10.1074/Jbc.M110.161794 |
0.603 |
|
| 2010 |
Das D, Luo X, Singh A, Gu Y, Ghosh S, Mukhopadhyay CK, Chen SG, Sy MS, Kong Q, Singh N. Paradoxical role of prion protein aggregates in redox-iron induced toxicity. Plos One. 5: e11420. PMID 20625431 DOI: 10.1371/Journal.Pone.0011420 |
0.368 |
|
| 2010 |
Yao C, El Khoury R, Wang W, Byrd TA, Pehek EA, Thacker C, Zhu X, Smith MA, Wilson-Delfosse AL, Chen SG. LRRK2-mediated neurodegeneration and dysfunction of dopaminergic neurons in a Caenorhabditis elegans model of Parkinson's disease. Neurobiology of Disease. 40: 73-81. PMID 20382224 DOI: 10.1016/J.Nbd.2010.04.002 |
0.58 |
|
| 2010 |
Lee HP, Zhu X, Liu G, Chen SG, Perry G, Smith MA, Lee HG. Divalent metal transporter, iron, and Parkinson's disease: a pathological relationship. Cell Research. 20: 397-9. PMID 20357807 DOI: 10.1038/Cr.2010.39 |
0.493 |
|
| 2009 |
Su B, Liu H, Wang X, Chen SG, Siedlak SL, Kondo E, Choi R, Takeda A, Castellani RJ, Perry G, Smith MA, Zhu X, Lee HG. Ectopic localization of FOXO3a protein in Lewy bodies in Lewy body dementia and Parkinson's disease. Molecular Neurodegeneration. 4: 32. PMID 19627592 DOI: 10.1186/1750-1326-4-32 |
0.563 |
|
| 2009 |
Hatcher K, Zheng J, Chen SG. Cryptic peptides of the kringle domains preferentially bind to disease-associated prion protein. Journal of Alzheimer's Disease : Jad. 16: 421-31. PMID 19221431 DOI: 10.3233/Jad-2009-0980 |
0.414 |
|
| 2009 |
Gandhi PN, Chen SG, Wilson-Delfosse AL. Leucine-rich repeat kinase 2 (LRRK2): a key player in the pathogenesis of Parkinson's disease. Journal of Neuroscience Research. 87: 1283-95. PMID 19025767 DOI: 10.1002/Jnr.21949 |
0.369 |
|
| 2009 |
Aliev G, Liu J, Shenk JC, Fischbach K, Pacheco GJ, Chen SG, Obrenovich ME, Ward WF, Richardson AG, Smith MA, Gasimov E, Perry G, Ames BN. Neuronal mitochondrial amelioration by feeding acetyl-L-carnitine and lipoic acid to aged rats. Journal of Cellular and Molecular Medicine. 13: 320-33. PMID 18373733 DOI: 10.1111/J.1582-4934.2008.00324.X |
0.473 |
|
| 2008 |
Perry G, Zhu X, Babar AK, Siedlak SL, Yang Q, Ito G, Iwatsubo T, Smith MA, Chen SG. Leucine-rich repeat kinase 2 colocalizes with alpha-synuclein in Parkinson's disease, but not tau-containing deposits in tauopathies. Neuro-Degenerative Diseases. 5: 222-4. PMID 18322396 DOI: 10.1159/000113708 |
0.589 |
|
| 2008 |
Gandhi PN, Wang X, Zhu X, Chen SG, Wilson-Delfosse AL. The Roc domain of leucine-rich repeat kinase 2 is sufficient for interaction with microtubules. Journal of Neuroscience Research. 86: 1711-20. PMID 18214993 DOI: 10.1002/Jnr.21622 |
0.355 |
|
| 2007 |
Guo L, Gandhi PN, Wang W, Petersen RB, Wilson-Delfosse AL, Chen SG. The Parkinson's disease-associated protein, leucine-rich repeat kinase 2 (LRRK2), is an authentic GTPase that stimulates kinase activity. Experimental Cell Research. 313: 3658-70. PMID 17706965 DOI: 10.1016/J.Yexcr.2007.07.007 |
0.349 |
|
| 2007 |
Huang S, Liang J, Zheng M, Li X, Wang M, Wang P, Vanegas D, Wu D, Chakraborty B, Hays AP, Chen K, Chen SG, Booth S, Cohen M, Gambetti P, et al. Inducible overexpression of wild-type prion protein in the muscles leads to a primary myopathy in transgenic mice. Proceedings of the National Academy of Sciences of the United States of America. 104: 6800-5. PMID 17420473 DOI: 10.1073/Pnas.0608885104 |
0.533 |
|
| 2006 |
Hatcher K, Harris C, Gambetti P, Chen SG. Advances in Prion Disease Surveillance. Advances in Clinical Chemistry. 41: 263-292. PMID 28682752 DOI: 10.1016/S0065-2423(05)41008-2 |
0.603 |
|
| 2006 |
Zhu X, Babar A, Siedlak SL, Yang Q, Ito G, Iwatsubo T, Smith MA, Perry G, Chen SG. LRRK2 in Parkinson's disease and dementia with Lewy bodies. Molecular Neurodegeneration. 1: 17. PMID 17137507 DOI: 10.1186/1750-1326-1-17 |
0.549 |
|
| 2006 |
Obrenovich ME, Smith MA, Siedlak SL, Chen SG, de la Torre JC, Perry G, Aliev G. Overexpression of GRK2 in Alzheimer disease and in a chronic hypoperfusion rat model is an early marker of brain mitochondrial lesions. Neurotoxicity Research. 10: 43-56. PMID 17000469 DOI: 10.1007/Bf03033333 |
0.536 |
|
| 2006 |
Zhu X, Siedlak SL, Smith MA, Perry G, Chen SG. LRRK2 protein is a component of Lewy bodies. Annals of Neurology. 60: 617-8; author reply . PMID 16847950 DOI: 10.1002/Ana.20928 |
0.509 |
|
| 2006 |
Colucci M, Moleres FJ, Xie ZL, Ray-Chaudhury A, Gutti S, Butefisch CM, Cervenakova L, Wang W, Goldfarb LG, Kong Q, Ghetti B, Chen SG, Gambetti P. Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits. Journal of Neuropathology and Experimental Neurology. 65: 642-51. PMID 16825951 DOI: 10.1097/01.Jnen.0000228198.81797.4D |
0.617 |
|
| 2006 |
Xie Z, O'Rourke KI, Dong Z, Jenny AL, Langenberg JA, Belay ED, Schonberger LB, Petersen RB, Zou W, Kong Q, Gambetti P, Chen SG. Chronic wasting disease of elk and deer and Creutzfeldt-Jakob disease: comparative analysis of the scrapie prion protein. The Journal of Biological Chemistry. 281: 4199-206. PMID 16338930 DOI: 10.1074/Jbc.M509052200 |
0.656 |
|
| 2006 |
Guo L, Wang W, Gandhi PN, Wilson-Delfosse AL, Chen SG. P1-423: Functional studies of a novel protein kinase LRRK2 provide insights into pathogenesis of Parkinson's disease Alzheimer's & Dementia. 2: S221-S222. DOI: 10.1016/J.Jalz.2006.05.802 |
0.371 |
|
| 2006 |
Smith MA, Zhu X, Babar A, Siedlak SL, Yang Q, Ito G, Iwatsubo T, Perry G, Chen SG. P4-162: LRRK2 in Lewy bodies of Parkinson's disease and dementia with Lewy bodies Alzheimer's & Dementia. 2: S564-S564. DOI: 10.1016/J.Jalz.2006.05.1901 |
0.45 |
|
| 2005 |
Pastore M, Chin SS, Bell KL, Dong Z, Yang Q, Yang L, Yuan J, Chen SG, Gambetti P, Zou WQ. Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD. The American Journal of Pathology. 167: 1729-38. PMID 16314483 DOI: 10.1016/S0002-9440(10)61254-0 |
0.64 |
|
| 2005 |
Kong Q, Huang S, Zou W, Vanegas D, Wang M, Wu D, Yuan J, Zheng M, Bai H, Deng H, Chen K, Jenny AL, O'Rourke K, Belay ED, Schonberger LB, ... ... Chen SG, et al. Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 7944-9. PMID 16135751 DOI: 10.1523/Jneurosci.2467-05.2005 |
0.6 |
|
| 2005 |
Narang HK, Dagdanova A, Xie Z, Yang Q, Chen SG. Sensitive detection of prion protein in human urine. Experimental Biology and Medicine (Maywood, N.J.). 230: 343-9. PMID 15855301 DOI: 10.1177/153537020523000508 |
0.345 |
|
| 2005 |
Aliyev A, Chen SG, Seyidova D, Smith MA, Perry G, de la Torre J, Aliev G. Mitochondria DNA deletions in atherosclerotic hypoperfused brain microvessels as a primary target for the development of Alzheimer's disease. Journal of the Neurological Sciences. 229: 285-92. PMID 15760652 DOI: 10.1016/J.Jns.2004.11.040 |
0.543 |
|
| 2005 |
Aliev G, Perry G, Liu J, Smith MA, Chen SG, Ames BN, de la Torre JC. [P-074]: The primary pathogenetic role of vascular contains vasoactive substances, hypoperfusion, mitochondria failure and oxidative stress in aging and Alzheimer disease Alzheimer's & Dementia. 1: S31-S31. DOI: 10.1016/J.Jalz.2005.06.148 |
0.511 |
|
| 2004 |
Mishra RS, Basu S, Gu Y, Luo X, Zou WQ, Mishra R, Li R, Chen SG, Gambetti P, Fujioka H, Singh N. Protease-resistant human prion protein and ferritin are cotransported across Caco-2 epithelial cells: implications for species barrier in prion uptake from the intestine. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 11280-90. PMID 15601934 DOI: 10.1523/Jneurosci.2864-04.2004 |
0.606 |
|
| 2004 |
Aliyev A, Seyidova D, Rzayev N, Obrenovich ME, Lamb BT, Chen SG, Smith MA, Perry G, de la Torre JC, Aliev G. Is nitric oxide a key target in the pathogenesis of brain lesions during the development of Alzheimer's disease? Neurological Research. 26: 547-53. PMID 15265272 DOI: 10.1179/01610425017613 |
0.529 |
|
| 2004 |
Zou WQ, Zheng J, Gray DM, Gambetti P, Chen SG. Antibody to DNA detects scrapie but not normal prion protein. Proceedings of the National Academy of Sciences of the United States of America. 101: 1380-5. PMID 14734804 DOI: 10.1073/Pnas.0307825100 |
0.627 |
|
| 2004 |
Atwood CS, Perry G, Zeng H, Kato Y, Jones WD, Ling KQ, Huang X, Moir RD, Wang D, Sayre LM, Smith MA, Chen SG, Bush AI. Copper mediates dityrosine cross-linking of Alzheimer's amyloid-beta. Biochemistry. 43: 560-8. PMID 14717612 DOI: 10.1021/Bi0358824 |
0.501 |
|
| 2004 |
Kong Q, Surewicz WK, Petersen RB, Zou W, Chen SG, Gambetti P, Parchi P, Capellari S, Goldfarb L, Montagna P, Lugaresi E, Piccardo P, Ghetti B. 14 Inherited Prion Diseases Cold Spring Harbor Monograph Archive. 41: 673-775. DOI: 10.1101/087969693.41.673 |
0.576 |
|
| 2003 |
Gambetti P, Kong Q, Zou W, Parchi P, Chen SG. Sporadic and familial CJD: classification and characterisation. British Medical Bulletin. 66: 213-39. PMID 14522861 DOI: 10.1093/Bmb/66.1.213 |
0.619 |
|
| 2003 |
Zou WQ, Capellari S, Parchi P, Sy MS, Gambetti P, Chen SG. Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease. The Journal of Biological Chemistry. 278: 40429-36. PMID 12917418 DOI: 10.1074/Jbc.M308550200 |
0.64 |
|
| 2003 |
Gambetti P, Parchi P, Chen SG. Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia. Clinics in Laboratory Medicine. 23: 43-64. PMID 12733424 DOI: 10.1016/S0272-2712(02)00065-3 |
0.66 |
|
| 2003 |
Zou W, Colucci M, Gambetti P, Chen SG. Characterization of prion proteins. Methods in Molecular Biology (Clifton, N.J.). 217: 305-14. PMID 12491943 DOI: 10.1385/1-59259-330-5:305 |
0.56 |
|
| 2002 |
Chen SG, Gambetti P. A journey through the species barrier. Neuron. 34: 854-6. PMID 12086631 DOI: 10.1016/S0896-6273(02)00736-5 |
0.536 |
|
| 2002 |
Taratuto AL, Piccardo P, Reich EG, Chen SG, Sevlever G, Schultz M, Luzzi AA, Rugiero M, Abecasis G, Endelman M, Garcia AM, Capellari S, Xie Z, Lugaresi E, Gambetti P, et al. Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease. Neurology. 58: 362-7. PMID 11839833 DOI: 10.1212/Wnl.58.3.362 |
0.614 |
|
| 2001 |
Chen SG. Molecular profiling of paired helical filaments. Journal of Alzheimer's Disease : Jad. 3: 467-9. PMID 22391261 DOI: 10.3233/Jad-2001-3505 |
0.32 |
|
| 2001 |
Gambetti P, Parchi P, Capellari S, Russo C, Tabaton M, Teller JK, Chen SG. Mechanisms of phenotypic heterogeneity in prion, Alzheimer and other conformational diseases. Journal of Alzheimer's Disease : Jad. 3: 87-95. PMID 12214077 DOI: 10.3233/Jad-2001-3113 |
0.633 |
|
| 2001 |
Wong BS, Chen SG, Colucci M, Xie Z, Pan T, Liu T, Li R, Gambetti P, Sy MS, Brown DR. Aberrant metal binding by prion protein in human prion disease. Journal of Neurochemistry. 78: 1400-8. PMID 11579148 DOI: 10.1046/J.1471-4159.2001.00522.X |
0.622 |
|
| 2001 |
Pan T, Colucci M, Wong BS, Li R, Liu T, Petersen RB, Chen S, Gambetti P, Sy MS. Novel differences between two human prion strains revealed by two-dimensional gel electrophoresis. The Journal of Biological Chemistry. 276: 37284-8. PMID 11489910 DOI: 10.1074/Jbc.M107358200 |
0.559 |
|
| 2001 |
Wong BS, Green AJ, Li R, Xie Z, Pan T, Liu T, Chen SG, Gambetti P, Sy MS. Absence of protease-resistant prion protein in the cerebrospinal fluid of Creutzfeldt-Jakob disease. The Journal of Pathology. 194: 9-14. PMID 11329135 DOI: 10.1002/Path.872 |
0.625 |
|
| 2001 |
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. Induction of HO-1 and NOS in doppel-expressing mice devoid of PrP: implications for doppel function. Molecular and Cellular Neurosciences. 17: 768-75. PMID 11312611 DOI: 10.1006/Mcne.2001.0963 |
0.636 |
|
| 2000 |
Chen SG, Zou W, Parchi P, Gambetti P. PrP(Sc) typing by N-terminal sequencing and mass spectrometry. Archives of Virology. Supplementum. 209-16. PMID 11214924 DOI: 10.1007/978-3-7091-6308-5_20 |
0.423 |
|
| 2000 |
Lu K, Wang W, Xie Z, Wong BS, Li R, Petersen RB, Sy MS, Chen SG. Expression and structural characterization of the recombinant human doppel protein. Biochemistry. 39: 13575-83. PMID 11063595 DOI: 10.1021/Bi001523M |
0.361 |
|
| 2000 |
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. Genetic influence on the structural variations of the abnormal prion protein. Proceedings of the National Academy of Sciences of the United States of America. 97: 10168-72. PMID 10963679 DOI: 10.1073/Pnas.97.18.10168 |
0.609 |
|
| 2000 |
Swietnicki W, Morillas M, Chen SG, Gambetti P, Surewicz WK. Aggregation and fibrillization of the recombinant human prion protein huPrP90-231. Biochemistry. 39: 424-31. PMID 10631004 DOI: 10.1021/Bi991967M |
0.579 |
|
| 1999 |
Goedert M, Spillantini MG, Crowther RA, Chen SG, Parchi P, Tabaton M, Lanska DJ, Markesbery WR, Wilhelmsen KC, Dickson DW, Petersen RB, Gambetti P. Tau gene mutation in familial progressive subcortical gliosis. Nature Medicine. 5: 454-7. PMID 10202939 DOI: 10.1038/7454 |
0.319 |
|
| 1999 |
Gambetti P, Petersen RB, Parchi P, Chen SG, Capellari S, Goldfarb L, Gabizon R, Montagna P, Lugaresi E, Piccardo P, Ghetti B. 13 Inherited Prion Diseases Cold Spring Harbor Monograph Archive. 38: 509-583. DOI: 10.1101/087969547.38.509 |
0.573 |
|
| 1998 |
Russo C, Angelini G, Dapino D, Piccini A, Piombo G, Schettini G, Chen S, Teller JK, Zaccheo D, Gambetti P, Tabaton M. Opposite roles of apolipoprotein E in normal brains and in Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America. 95: 15598-602. PMID 9861015 DOI: 10.1073/Pnas.95.26.15598 |
0.47 |
|
| 1998 |
Parchi P, Petersen RB, Chen SG, Autilio-Gambetti L, Capellari S, Monari L, Cortelli P, Montagna P, Lugaresi E, Gambetti P. Molecular pathology of fatal familial insomnia. Brain Pathology (Zurich, Switzerland). 8: 539-48. PMID 9669705 DOI: 10.1111/J.1750-3639.1998.Tb00176.X |
0.624 |
|
| 1998 |
Parchi P, Chen SG, Brown P, Zou W, Capellari S, Budka H, Hainfellner J, Reyes PF, Golden GT, Hauw JJ, Gajdusek DC, Gambetti P. Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease. Proceedings of the National Academy of Sciences of the United States of America. 95: 8322-7. PMID 9653185 DOI: 10.1073/Pnas.95.14.8322 |
0.471 |
|
| 1997 |
Singh N, Zanusso G, Chen SG, Fujioka H, Richardson S, Gambetti P, Petersen RB. Prion protein aggregation reverted by low temperature in transfected cells carrying a prion protein gene mutation. The Journal of Biological Chemistry. 272: 28461-70. PMID 9353306 DOI: 10.1074/Jbc.272.45.28461 |
0.635 |
|
| 1997 |
Chen SG, Parchi P, Brown P, Capellari S, Zou W, Cochran EJ, Vnencak-Jones CL, Julien J, Vital C, Mikol J, Lugaresi E, Autilio-Gambetti L, Gambetti P. Allelic origin of the abnormal prion protein isoform in familial prion diseases. Nature Medicine. 3: 1009-15. PMID 9288728 DOI: 10.1038/Nm0997-1009 |
0.63 |
|
| 1997 |
Raymond GJ, Hope J, Kocisko DA, Priola SA, Raymond LD, Bossers A, Ironside J, Will RG, Chen SG, Petersen RB, Gambetti P, Rubenstein R, Smits MA, Lansbury PT, Caughey B. Molecular assessment of the potential transmissibilities of BSE and scrapie to humans. Nature. 388: 285-8. PMID 9230438 DOI: 10.1038/40876 |
0.604 |
|
| 1996 |
Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, Farlow M, Dickson DW, Sima AA, Trojanowski JQ, Petersen RB, Gambetti P. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Annals of Neurology. 39: 767-78. PMID 8651649 DOI: 10.1002/Ana.410390613 |
0.637 |
|
| 1996 |
Parchi P, Capellari S, Sima AA, DʼAmato C, McKeever P, Mikol J, Brion S, Brown P, Chen SG, Petersen RB, Gambetti P. CREUTZFELDT-JAKOB DISEASE (CJD) WITH 178ASN MUTATION IN THE PRION PROTEIN GENE Journal of Neuropathology and Experimental Neurology. 55: 635. DOI: 10.1097/00005072-199605000-00132 |
0.394 |
|
| 1995 |
Gambetti P, Parchi P, Petersen RB, Chen SG, Lugaresi E. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features. Brain Pathology (Zurich, Switzerland). 5: 43-51. PMID 7767490 DOI: 10.1111/J.1750-3639.1995.Tb00576.X |
0.609 |
|
| 1995 |
Chen SG, Teplow DB, Parchi P, Teller JK, Gambetti P, Autilio-Gambetti L. Truncated forms of the human prion protein in normal brain and in prion diseases. The Journal of Biological Chemistry. 270: 19173-80. PMID 7642585 DOI: 10.1074/Jbc.270.32.19173 |
0.6 |
|
| 1995 |
Parchi P, Castellani R, Cortelli P, Montagna P, Chen SG, Petersen RB, Manetto V, Vnencak-Jones CL, McLean MJ, Sheller JR. Regional distribution of protease-resistant prion protein in fatal familial insomnia. Annals of Neurology. 38: 21-9. PMID 7611720 DOI: 10.1002/Ana.410380107 |
0.4 |
|
| 1995 |
Parchi P, Castellani R, Capellari S, Petersen RB, Chen SG, Younq K, Farlow M, Troianowski JQ, Sima A, Ghetti B, Gambetti P. PROTEASE-RESISTANT PRION PROTEIN IN SPORADIC CREUTZFELDT-JAKOB DISEASE (CJD) Journal of Neuropathology and Experimental Neurology. 54: 416. DOI: 10.1097/00005072-199505000-00035 |
0.414 |
|
| 1994 |
Monari L, Chen SG, Brown P, Parchi P, Petersen RB, Mikol J, Gray F, Cortelli P, Montagna P, Ghetti B. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism. Proceedings of the National Academy of Sciences of the United States of America. 91: 2839-42. PMID 7908444 DOI: 10.1073/Pnas.91.7.2839 |
0.455 |
|
| 1993 |
Monari L, Petersen RB, Chen SG, Cortelli P, Montagna P, Berg L, Julien J, Lugaresi E, Autilio-Gambetti L, Gambetti P. Detection of prion protein in fibroblasts from two Fatal Familial Insomnia kindred Journal of Neuropathology and Experimental Neurology. 52: 293. DOI: 10.1097/00005072-199305000-00133 |
0.308 |
|
| Show low-probability matches. |
