| Year |
Citation |
Score |
| 2020 |
Asante EA, Linehan JM, Tomlinson A, Jakubcova T, Hamdan S, Grimshaw A, Smidak M, Jeelani A, Nihat A, Mead S, Brandner S, Wadsworth JDF, Collinge J. Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS. Plos Biology. 18: e3000725. PMID 32516343 DOI: 10.1371/Journal.Pbio.3000725 |
0.397 |
|
| 2020 |
Schottlaender LV, Abeti R, Jaunmuktane Z, Macmillan C, Chelban V, O'Callaghan B, McKinley J, Maroofian R, Efthymiou S, Athanasiou-Fragkouli A, Forbes R, Soutar MPM, Livingston JH, Kalmar B, Swayne O, ... ... Brandner S, et al. Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification. American Journal of Human Genetics. 106: 412-421. PMID 32142645 DOI: 10.1016/J.Ajhg.2020.02.007 |
0.348 |
|
| 2020 |
Ricci B, Millner TO, Pomella N, Zhang X, Guglielmi L, Badodi S, Ceric D, Gemma C, Cognolato E, Zhang Y, Brandner S, Barnes MR, Marino S. Polycomb-mediated repression of EphrinA5 promotes growth and invasion of glioblastoma. Oncogene. PMID 31988455 DOI: 10.1038/S41388-020-1161-3 |
0.303 |
|
| 2020 |
Jaunmuktane Z, Brandner S. Invited Review: The role of prion-like mechanisms in neurodegenerative diseases. Neuropathology and Applied Neurobiology. PMID 31868945 DOI: 10.1111/Nan.12592 |
0.329 |
|
| 2019 |
Bödör C, Alpár D, Marosvári D, Galik B, Rajnai H, Bátai B, Nagy Á, Kajtár B, Burján A, Deák B, Schneider T, Alizadeh H, Matolcsy A, Brandner S, Storhoff J, et al. Molecular Subtypes and Genomic Profile of Primary Central Nervous System Lymphoma. Journal of Neuropathology and Experimental Neurology. PMID 31886867 DOI: 10.1093/Jnen/Nlz125 |
0.328 |
|
| 2019 |
Katrak SM, Pauranik A, Desai SB, Mead S, Beck J, Brandner S, Collinge J. Familial Creutzfeldt-Jakob Disease in an Indian Kindred. Annals of Indian Academy of Neurology. 22: 458-461. PMID 31736569 DOI: 10.4103/Aian.Aian_214_19 |
0.356 |
|
| 2019 |
Sievers P, Appay R, Schrimpf D, Stichel D, Reuss DE, Wefers AK, Reinhardt A, Coras R, Ruf VC, Schmid S, de Stricker K, Boldt HB, Kristensen BW, Petersen JK, Ulhøi BP, ... ... Brandner S, et al. Rosette-forming glioneuronal tumors share a distinct DNA methylation profile and mutations in FGFR1, with recurrent co-mutation of PIK3CA and NF1. Acta Neuropathologica. PMID 31250151 DOI: 10.1007/S00401-019-02038-4 |
0.324 |
|
| 2019 |
Rudge P, Jaunmuktane Z, Hyare H, Ellis M, Koltzenburg M, Collinge J, Brandner S, Mead S. Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease. Brain : a Journal of Neurology. PMID 30698738 DOI: 10.1093/Brain/Awy358 |
0.335 |
|
| 2019 |
Brandner S, Jaunmuktane Z. IDH mutant astrocytoma: biomarkers for prognostic stratification and the next frontiers Neuropathology and Applied Neurobiology. 45: 91-94. PMID 30326147 DOI: 10.1111/Nan.12521 |
0.339 |
|
| 2019 |
Jaunmuktane Z, Brandner S. Transmissible human proteopathies: an expanding field Diagnostic Histopathology. 25: 16-22. DOI: 10.1016/J.Mpdhp.2018.11.002 |
0.312 |
|
| 2018 |
Purro SA, Farrow MA, Linehan J, Nazari T, Thomas DX, Chen Z, Mengel D, Saito T, Saido T, Rudge P, Brandner S, Walsh DM, Collinge J. Transmission of amyloid-β protein pathology from cadaveric pituitary growth hormone. Nature. PMID 30546139 DOI: 10.1038/S41586-018-0790-Y |
0.316 |
|
| 2018 |
Stichel D, Ebrahimi A, Reuss D, Schrimpf D, Ono T, Shirahata M, Reifenberger G, Weller M, Hänggi D, Wick W, Herold-Mende C, Westphal M, Brandner S, Pfister SM, Capper D, et al. Distribution of EGFR amplification, combined chromosome 7 gain and chromosome 10 loss, and TERT promoter mutation in brain tumors and their potential for the reclassification of IDHwt astrocytoma to glioblastoma. Acta Neuropathologica. PMID 30187121 DOI: 10.1007/S00401-018-1905-0 |
0.3 |
|
| 2018 |
Massaro G, Mattar CNZ, Wong AMS, Sirka E, Buckley SMK, Herbert BR, Karlsson S, Perocheau DP, Burke D, Heales S, Richard-Londt A, Brandner S, Huebecker M, Priestman DA, Platt FM, et al. Fetal gene therapy for neurodegenerative disease of infants. Nature Medicine. PMID 30013199 DOI: 10.1038/S41591-018-0106-7 |
0.362 |
|
| 2018 |
Deng MY, Sill M, Chiang J, Schittenhelm J, Ebinger M, Schuhmann MU, Monoranu CM, Milde T, Wittmann A, Hartmann C, Sommer C, Paulus W, Gärtner J, Brück W, Rüdiger T, ... ... Brandner S, et al. Molecularly defined diffuse leptomeningeal glioneuronal tumor (DLGNT) comprises two subgroups with distinct clinical and genetic features. Acta Neuropathologica. PMID 29766299 DOI: 10.1007/S00401-018-1865-4 |
0.312 |
|
| 2018 |
Li N, Zhang Y, Sidlauskas K, Ellis M, Evans I, Frankel P, Lau J, El-Hassan T, Guglielmi L, Broni J, Richard-Loendt A, Brandner S. Inhibition of GPR158 by microRNA-449a suppresses neural lineage of glioma stem/progenitor cells and correlates with higher glioma grades. Oncogene. PMID 29720725 DOI: 10.1038/S41388-018-0277-1 |
0.308 |
|
| 2018 |
Jaunmuktane Z, Quaegebeur A, Taipa R, Viana-Baptista M, Barbosa R, Koriath C, Sciot R, Mead S, Brandner S. Evidence of amyloid-β cerebral amyloid angiopathy transmission through neurosurgery Acta Neuropathologica. 135: 671-679. PMID 29450646 DOI: 10.1007/S00401-018-1822-2 |
0.324 |
|
| 2018 |
Joiner S, Asante EA, Linehan JM, Brock L, Brandner S, Bellworthy SJ, Simmons MM, Hope J, Collinge J, Wadsworth JDF. Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein. Journal of the Neurological Sciences. 386: 4-11. PMID 29406965 DOI: 10.1016/J.Jns.2017.12.038 |
0.364 |
|
| 2017 |
Pathania M, De Jay N, Maestro N, Harutyunyan AS, Nitarska J, Pahlavan P, Henderson S, Mikael LG, Richard-Londt A, Zhang Y, Costa JR, Hébert S, Khazaei S, Ibrahim NS, Herrero J, ... ... Brandner S, et al. H3.3(K27M) Cooperates with Trp53 Loss and PDGFRA Gain in Mouse Embryonic Neural Progenitor Cells to Induce Invasive High-Grade Gliomas. Cancer Cell. PMID 29107533 DOI: 10.1016/J.Ccell.2017.09.014 |
0.307 |
|
| 2017 |
Tarpey PS, Behjati S, Young MD, Martincorena I, Alexandrov LB, Farndon SJ, Guzzo C, Hardy C, Latimer C, Butler AP, Teague JW, Shlien A, Futreal PA, Shah S, Bashashati A, ... ... Brandner S, et al. The driver landscape of sporadic chordoma. Nature Communications. 8: 890. PMID 29026114 DOI: 10.1038/S41467-017-01026-0 |
0.306 |
|
| 2017 |
Wadsworth JDF, Adamson G, Joiner S, Brock L, Powell C, Linehan JM, Beck JA, Brandner S, Mead S, Collinge J. Methods for Molecular Diagnosis of Human Prion Disease. Methods in Molecular Biology (Clifton, N.J.). 1658: 311-346. PMID 28861799 DOI: 10.1007/978-1-4939-7244-9_22 |
0.369 |
|
| 2017 |
Kulshrestha R, Burton-Jones S, Antoniadi T, Rogers M, Jaunmuktane Z, Brandner S, Kiely N, Manuel R, Willis T. Deletion of P2 promoter of GJB1 gene a cause of Charcot-Marie-Tooth disease. Neuromuscular Disorders : Nmd. PMID 28601552 DOI: 10.1016/J.Nmd.2017.05.001 |
0.324 |
|
| 2017 |
Haston S, Pozzi S, Carreno G, Manshaei S, Panousopoulos L, Gonzalez-Meljem JM, Apps JR, Virasami A, Thavaraj S, Gutteridge A, Forshew T, Marais R, Brandner S, Jacques TS, Andoniadou CL, et al. MAPK pathway control of stem cell proliferation and differentiation in the embryonic pituitary provides insights into the pathogenesis of papillary craniopharyngioma. Development. 144: 2141-2152. PMID 28506993 DOI: 10.1242/Dev.150490 |
0.302 |
|
| 2017 |
Horga A, Laurà M, Jaunmuktane Z, Jerath NU, Gonzalez MA, Polke JM, Poh R, Blake JC, Liu YT, Wiethoff S, Bettencourt C, Lunn MP, Manji H, Hanna MG, Houlden H, ... Brandner S, et al. Genetic and clinical characteristics of NEFL-related Charcot-Marie-Tooth disease. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 28501821 DOI: 10.1136/Jnnp-2016-315077 |
0.321 |
|
| 2017 |
Cummings DM, Benway TA, Ho H, Tedoldi A, Fernandes Freitas MM, Shahab L, Murray CE, Richard-Loendt A, Brandner S, Lashley T, Salih DA, Edwards FA. Neuronal and Peripheral Pentraxins Modify Glutamate Release and may Interact in Blood-Brain Barrier Failure. Cerebral Cortex (New York, N.Y. : 1991). 1-12. PMID 28334103 DOI: 10.1093/Cercor/Bhx046 |
0.313 |
|
| 2017 |
Mok T, Jaunmuktane Z, Joiner S, Campbell T, Morgan C, Wakerley B, Golestani F, Rudge P, Mead S, Jäger HR, Wadsworth JD, Brandner S, Collinge J. Variant Creutzfeldt-Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129. The New England Journal of Medicine. 376: 292-294. PMID 28099827 DOI: 10.1056/Nejmc1610003 |
0.344 |
|
| 2017 |
Brandner S, Jaunmuktane Z. Prion disease: experimental models and reality. Acta Neuropathologica. 133: 197-222. PMID 28084518 DOI: 10.1007/S00401-017-1670-5 |
0.332 |
|
| 2016 |
Kara E, Tucci A, Manzoni C, Lynch DS, Elpidorou M, Bettencourt C, Chelban V, Manole A, Hamed SA, Haridy NA, Federoff M, Preza E, Hughes D, Pittman A, Jaunmuktane Z, ... Brandner S, et al. Genetic and phenotypic characterization of complex hereditary spastic paraplegia. Brain : a Journal of Neurology. PMID 27217339 DOI: 10.1093/Brain/Aww111 |
0.353 |
|
| 2016 |
Mead S, Burnell M, Lowe J, Thompson A, Lukic A, Porter MC, Carswell C, Kaski D, Kenny J, Mok TH, Bjurstrom N, Franko E, Gorham M, Druyeh R, Wadsworth JD, ... ... Brandner S, et al. Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob Disease. Jama Neurology. PMID 26902324 DOI: 10.1001/Jamaneurol.2015.4885 |
0.33 |
|
| 2016 |
Benedykcinska A, Ferreira A, Lau J, Broni J, Richard-Loendt A, Henriquez NV, Brandner S. Generation of brain tumours in mice by Cre-mediated recombination of neural progenitors in situ with the tamoxifen metabolite endoxifen Dmm Disease Models and Mechanisms. 9: 211-220. DOI: 10.1242/Dmm.022715 |
0.34 |
|
| 2015 |
McKinnon C, Goold R, Andre R, Devoy A, Ortega Z, Moonga J, Linehan JM, Brandner S, Lucas JJ, Collinge J, Tabrizi SJ. Prion-mediated neurodegeneration is associated with early impairment of the ubiquitin-proteasome system. Acta Neuropathologica. PMID 26646779 DOI: 10.1007/S00401-015-1508-Y |
0.358 |
|
| 2015 |
Schmidt C, Fizet J, Properzi F, Batchelor M, Sandberg MK, Edgeworth JA, Afran L, Ho S, Badhan A, Klier S, Linehan JM, Brandner S, Hosszu LL, Tattum MH, Jat P, et al. A systematic investigation of production of synthetic prions from recombinant prion protein. Open Biology. 5. PMID 26631378 DOI: 10.1098/Rsob.150165 |
0.31 |
|
| 2015 |
Eisenmenger L, Porter MC, Carswell CJ, Thompson A, Mead S, Rudge P, Collinge J, Brandner S, Jäger HR, Hyare H. Evolution of Diffusion-Weighted Magnetic Resonance Imaging Signal Abnormality in Sporadic Creutzfeldt-Jakob Disease, With Histopathological Correlation. Jama Neurology. 1-9. PMID 26569479 DOI: 10.1001/Jamaneurol.2015.3159 |
0.316 |
|
| 2015 |
Jaunmuktane Z, Mead S, Ellis M, Wadsworth JD, Nicoll AJ, Kenny J, Launchbury F, Linehan J, Richard-Loendt A, Walker AS, Rudge P, Collinge J, Brandner S. Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy. Nature. 525: 247-50. PMID 26354483 DOI: 10.1038/Nature15369 |
0.346 |
|
| 2015 |
Rudge P, Jaunmuktane Z, Adlard P, Bjurstrom N, Caine D, Lowe J, Norsworthy P, Hummerich H, Druyeh R, Wadsworth JD, Brandner S, Hyare H, Mead S, Collinge J. Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years. Brain : a Journal of Neurology. 138: 3386-99. PMID 26268531 DOI: 10.1093/Brain/Awv235 |
0.365 |
|
| 2015 |
Saunus JM, Quinn MC, Patch AM, Pearson JV, Bailey PJ, Nones K, McCart Reed AE, Miller D, Wilson PJ, Al-Ejeh F, Mariasegaram M, Lau Q, Withers T, Jeffree RL, Reid LE, ... ... Brandner S, et al. Integrated genomic and transcriptomic analysis of human brain metastases identifies alterations of potential clinical significance. The Journal of Pathology. PMID 26172396 DOI: 10.1002/Path.4583 |
0.31 |
|
| 2015 |
Asante EA, Grimshaw A, Smidak M, Jakubcova T, Tomlinson A, Jeelani A, Hamdan S, Powell C, Joiner S, Linehan JM, Brandner S, Wadsworth JD, Collinge J. Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS. Plos Pathogens. 11: e1004953. PMID 26135918 DOI: 10.1371/Journal.Ppat.1004953 |
0.354 |
|
| 2015 |
Asante EA, Smidak M, Grimshaw A, Houghton R, Tomlinson A, Jeelani A, Jakubcova T, Hamdan S, Richard-Londt A, Linehan JM, Brandner S, Alpers M, Whitfield J, Mead S, Wadsworth JD, et al. A naturally occurring variant of the human prion protein completely prevents prion disease. Nature. 522: 478-81. PMID 26061765 DOI: 10.1038/Nature14510 |
0.372 |
|
| 2015 |
Lynch DS, Jaunmuktane Z, Sheerin UM, Phadke R, Brandner S, Milonas I, Dean A, Bajaj N, McNicholas N, Costello D, Cronin S, McGuigan C, Rossor M, Fox N, Murphy E, et al. Hereditary leukoencephalopathy with axonal spheroids: a spectrum of phenotypes from CNS vasculitis to parkinsonism in an adult onset leukodystrophy series. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 25935893 DOI: 10.1136/Jnnp-2015-310788 |
0.322 |
|
| 2015 |
Hyare H, So PW, Brandner S, Collinge J, Parkes HG. MRI detection of prion protein plaques in variant Creutzfeldt-Jakob disease. Neurology. 84: 1498-9. PMID 25846996 DOI: 10.1212/Wnl.0000000000000304 |
0.331 |
|
| 2015 |
Carr AS, Pelayo-Negro AL, Jaunmuktane Z, Scalco RS, Hutt D, Evans MR, Heally E, Brandner S, Holton J, Blake J, Whelan CJ, Wechalekar AD, Gillmore JD, Hawkins PN, Reilly MM. Transthyretin V122I amyloidosis with clinical and histological evidence of amyloid neuropathy and myopathy. Neuromuscular Disorders : Nmd. 25: 511-5. PMID 25819286 DOI: 10.1016/J.Nmd.2015.02.001 |
0.306 |
|
| 2015 |
Joyce PI, Mcgoldrick P, Saccon RA, Weber W, Fratta P, West SJ, Zhu N, Carter S, Phatak V, Stewart M, Simon M, Kumar S, Heise I, Bros-Facer V, Dick J, ... ... Brandner S, et al. A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity. Human Molecular Genetics. 24: 1883-97. PMID 25468678 DOI: 10.1093/Hmg/Ddu605 |
0.353 |
|
| 2015 |
Mirabile I, Jat PS, Brandner S, Collinge J. Identification of clinical target areas in the brainstem of prion-infected mice. Neuropathology and Applied Neurobiology. 41: 613-30. PMID 25311251 DOI: 10.1111/Nan.12189 |
0.301 |
|
| 2015 |
Li N, Sidlauskas K, Brandner S. Po26Microrna-449A Is Important For Impeding The Growth And Invasion Of Tumour Initiating Cells In Experimental Brain Tumour Models Neuro-Oncology. 17. DOI: 10.1093/Neuonc/Nov284.22 |
0.34 |
|
| 2014 |
Cottenie E, Kochanski A, Jordanova A, Bansagi B, Zimon M, Horga A, Jaunmuktane Z, Saveri P, Rasic VM, Baets J, Bartsakoulia M, Ploski R, Teterycz P, Nikolic M, Quinlivan R, ... ... Brandner S, et al. Truncating and missense mutations in IGHMBP2 cause Charcot-Marie Tooth disease type 2. American Journal of Human Genetics. 95: 590-601. PMID 25439726 DOI: 10.1016/J.Ajhg.2014.10.002 |
0.337 |
|
| 2014 |
Liu YT, Laurá M, Hersheson J, Horga A, Jaunmuktane Z, Brandner S, Pittman A, Hughes D, Polke JM, Sweeney MG, Proukakis C, Janssen JC, Auer-Grumbach M, Zuchner S, Shields KG, et al. Extended phenotypic spectrum of KIF5A mutations: From spastic paraplegia to axonal neuropathy. Neurology. 83: 612-9. PMID 25008398 DOI: 10.1212/Wnl.0000000000000691 |
0.319 |
|
| 2014 |
Grizenkova J, Akhtar S, Brandner S, Collinge J, Lloyd SE. Microglial Cx3cr1 knockout reduces prion disease incubation time in mice. Bmc Neuroscience. 15: 44. PMID 24655482 DOI: 10.1186/1471-2202-15-44 |
0.357 |
|
| 2014 |
Ricketts T, McGoldrick P, Fratta P, de Oliveira HM, Kent R, Phatak V, Brandner S, Blanco G, Greensmith L, Acevedo-Arozena A, Fisher EM. A nonsense mutation in mouse Tardbp affects TDP43 alternative splicing activity and causes limb-clasping and body tone defects. Plos One. 9: e85962. PMID 24465814 DOI: 10.1371/Journal.Pone.0085962 |
0.355 |
|
| 2014 |
Mead S, Wadsworth JD, Porter MC, Linehan JM, Pietkiewicz W, Jackson GS, Brandner S, Collinge J. Variant Creutzfeldt-Jakob disease with extremely low lymphoreticular deposition of prion protein. Jama Neurology. 71: 340-3. PMID 24445428 DOI: 10.1001/Jamaneurol.2013.5378 |
0.353 |
|
| 2014 |
Foley AR, Menezes MP, Pandraud A, Gonzalez MA, Al-Odaib A, Abrams AJ, Sugano K, Yonezawa A, Manzur AY, Burns J, Hughes I, McCullagh BG, Jungbluth H, Lim MJ, Lin JP, ... ... Brandner S, et al. Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2. Brain : a Journal of Neurology. 137: 44-56. PMID 24253200 DOI: 10.1093/Brain/Awt315 |
0.341 |
|
| 2014 |
Tucci A, Liu YT, Preza E, Pitceathly RD, Chalasani A, Plagnol V, Land JM, Trabzuni D, Ryten M, Jaunmuktane Z, Reilly MM, Brandner S, Hargreaves I, Hardy J, et al. Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophy. Journal of Neurology, Neurosurgery, and Psychiatry. 85: 486-92. PMID 24198383 DOI: 10.1136/Jnnp-2013-306387 |
0.335 |
|
| 2014 |
Sidlauskas K, Li N, Lau J, Ferreira A, Brandner S. O03Idh1 Mutations In Neural Stem Cells Promote Migration And Invasion And Act Synergistically With P53 And Pten Loss In Murine Tumour Cells Neuro-Oncology. 16. DOI: 10.1093/Neuonc/Nou250.3 |
0.341 |
|
| 2014 |
Brandner S, Benedykcinska A, Li N, Henriquez N. Novel Approach To Model Brain Tumours By Inducing Locally Restricted And Stem Cell Selective Gene Targeting. Neuro-Oncology. 16. DOI: 10.1093/Neuonc/Nou206.25 |
0.324 |
|
| 2014 |
Brandner S, Henriquez N, Benedykcinska A, Li N, Lau J, Sidlauskas K. O4.10Cns Stem Cell Specific Tumourigenesis Reveals Lineage Relationship Between Experimental And Human Gliomas And A Dominance Of Glial Signatures During Tumour Propagation In Vitro Neuro-Oncology. 16. DOI: 10.1093/Neuonc/Nou174.31 |
0.355 |
|
| 2013 |
Reiniger L, Mirabile I, Lukic A, Wadsworth JD, Linehan JM, Groves M, Lowe J, Druyeh R, Rudge P, Collinge J, Mead S, Brandner S. Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases. Acta Neuropathologica Communications. 1: 8. PMID 24252267 DOI: 10.1186/2051-5960-1-8 |
0.366 |
|
| 2013 |
Mead S, Gandhi S, Beck J, Caine D, Gajulapalli D, Gallujipali D, Carswell C, Hyare H, Joiner S, Ayling H, Lashley T, Linehan JM, Al-Doujaily H, Sharps B, Revesz T, ... ... Brandner S, et al. A novel prion disease associated with diarrhea and autonomic neuropathy. The New England Journal of Medicine. 369: 1904-14. PMID 24224623 DOI: 10.1056/Nejmoa1214747 |
0.406 |
|
| 2013 |
Wadsworth JD, Joiner S, Linehan JM, Balkema-Buschmann A, Spiropoulos J, Simmons MM, Griffiths PC, Groschup MH, Hope J, Brandner S, Asante EA, Collinge J. Atypical scrapie prions from sheep and lack of disease in transgenic mice overexpressing human prion protein. Emerging Infectious Diseases. 19: 1731-9. PMID 24188521 DOI: 10.3201/Eid1911.121341 |
0.355 |
|
| 2013 |
Asante EA, Linehan JM, Smidak M, Tomlinson A, Grimshaw A, Jeelani A, Jakubcova T, Hamdan S, Powell C, Brandner S, Wadsworth JD, Collinge J. Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein. Plos Pathogens. 9: e1003643. PMID 24086135 DOI: 10.1371/Journal.Ppat.1003643 |
0.402 |
|
| 2013 |
Henriquez NV, Forshew T, Tatevossian R, Ellis M, Richard-Loendt A, Rogers H, Jacques TS, Reitboeck PG, Pearce K, Sheer D, Grundy RG, Brandner S. Comparative expression analysis reveals lineage relationships between human and murine gliomas and a dominance of glial signatures during tumor propagation in vitro. Cancer Research. 73: 5834-44. PMID 23887970 DOI: 10.1158/0008-5472.Can-13-1299 |
0.309 |
|
| 2013 |
Cottenie E, Menezes MP, Rossor AM, Morrow JM, Yousry TA, Dick DJ, Anderson JR, Jaunmuktane Z, Brandner S, Blake JC, Houlden H, Reilly MM. Rapidly progressive asymmetrical weakness in Charcot-Marie-Tooth disease type 4J resembles chronic inflammatory demyelinating polyneuropathy. Neuromuscular Disorders : Nmd. 23: 399-403. PMID 23489662 DOI: 10.1016/J.Nmd.2013.01.010 |
0.34 |
|
| 2013 |
Akhtar S, Grizenkova J, Wenborn A, Hummerich H, Fernandez de Marco M, Brandner S, Collinge J, Lloyd SE. Sod1 deficiency reduces incubation time in mouse models of prion disease. Plos One. 8: e54454. PMID 23349894 DOI: 10.1371/Journal.Pone.0054454 |
0.336 |
|
| 2013 |
Acquati S, Greco A, Licastro D, Bhagat H, Ceric D, Rossini Z, Grieve J, Shaked-Rabi M, Henriquez NV, Brandner S, Stupka E, Marino S. Epigenetic regulation of survivin by Bmi1 is cell type specific during corticogenesis and in gliomas. Stem Cells (Dayton, Ohio). 31: 190-202. PMID 23132836 DOI: 10.1002/Stem.1274 |
0.308 |
|
| 2012 |
Grizenkova J, Akhtar S, Hummerich H, Tomlinson A, Asante EA, Wenborn A, Fizet J, Poulter M, Wiseman FK, Fisher EM, Tybulewicz VL, Brandner S, Collinge J, Lloyd SE. Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice. Proceedings of the National Academy of Sciences of the United States of America. 109: 13722-7. PMID 22869728 DOI: 10.1073/Pnas.1208917109 |
0.358 |
|
| 2012 |
Ghazi-Noori S, Froud KE, Mizielinska S, Powell C, Smidak M, Fernandez de Marco M, O'Malley C, Farmer M, Parkinson N, Fisher EM, Asante EA, Brandner S, Collinge J, Isaacs AM. Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic mice. Brain : a Journal of Neurology. 135: 819-32. PMID 22366797 DOI: 10.1093/Brain/Aws006 |
0.362 |
|
| 2012 |
Castro-Seoane R, Hummerich H, Sweeting T, Tattum MH, Linehan JM, Fernandez de Marco M, Brandner S, Collinge J, Klöhn PC. Plasmacytoid dendritic cells sequester high prion titres at early stages of prion infection. Plos Pathogens. 8: e1002538. PMID 22359509 DOI: 10.1371/Journal.Ppat.1002538 |
0.31 |
|
| 2012 |
Davidson G, Murphy S, Polke J, Laura M, Salih M, Muntoni F, Blake J, Brandner S, Davies N, Horvath R, Price S, Donaghy M, Roberts M, Foulds N, Ramdharry G, et al. Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort. Journal of Neurology. 259: 1673-85. PMID 22302274 DOI: 10.1007/S00415-011-6397-Y |
0.316 |
|
| 2012 |
Klöhn PC, Farmer M, Linehan JM, O'Malley C, Fernandez de Marco M, Taylor W, Farrow M, Khalili-Shirazi A, Brandner S, Collinge J. PrP antibodies do not trigger mouse hippocampal neuron apoptosis. Science (New York, N.Y.). 335: 52. PMID 22223800 DOI: 10.1126/Science.1215579 |
0.32 |
|
| 2012 |
Hyare H, Ramlackhansingh A, Gelosa G, Edison P, Rudge P, Brandner S, Brooks DJ, Collinge J, Mead S. 11C-PiB PET does not detect PrP-amyloid in prion disease patients including variant Creutzfeldt-Jakob disease. Journal of Neurology, Neurosurgery, and Psychiatry. 83: 340-1. PMID 21478204 DOI: 10.1136/Jnnp.2010.233692 |
0.322 |
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| 2012 |
Murphy SM, Davidson GL, Brandner S, Houlden H, Reilly MM. Mutation in FAM134B causing severe hereditary sensory neuropathy. Journal of Neurology, Neurosurgery, and Psychiatry. 83: 119-20. PMID 21115472 DOI: 10.1136/Jnnp.2010.228965 |
0.324 |
|
| 2011 |
Akhtar S, Wenborn A, Brandner S, Collinge J, Lloyd SE. Sex effects in mouse prion disease incubation time. Plos One. 6: e28741. PMID 22174884 DOI: 10.1371/Journal.Pone.0028741 |
0.33 |
|
| 2011 |
Kaski DN, Pennington C, Beck J, Poulter M, Uphill J, Bishop MT, Linehan JM, O'Malley C, Wadsworth JD, Joiner S, Knight RS, Ironside JW, Brandner S, Collinge J, Mead S. Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factors. Brain : a Journal of Neurology. 134: 1829-38. PMID 21616973 DOI: 10.1093/Brain/Awr079 |
0.354 |
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| 2011 |
Murphy SM, Polke J, Manji H, Blake J, Reiniger L, Sweeney M, Houlden H, Brandner S, Reilly MM. A novel mutation in the nerve-specific 5'UTR of the GJB1 gene causes X-linked Charcot-Marie-Tooth disease. Journal of the Peripheral Nervous System : Jpns. 16: 65-70. PMID 21504505 DOI: 10.1111/J.1529-8027.2011.00321.X |
0.31 |
|
| 2011 |
Cleary JO, Wiseman FK, Norris FC, Price AN, Choy M, Tybulewicz VL, Ordidge RJ, Brandner S, Fisher EM, Lythgoe MF. Structural correlates of active-staining following magnetic resonance microscopy in the mouse brain. Neuroimage. 56: 974-83. PMID 21310249 DOI: 10.1016/J.Neuroimage.2011.01.082 |
0.312 |
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| 2011 |
Wadsworth JD, Dalmau-Mena I, Joiner S, Linehan JM, O'Malley C, Powell C, Brandner S, Asante EA, Ironside JW, Hilton DA, Collinge J. Effect of fixation on brain and lymphoreticular vCJD prions and bioassay of key positive specimens from a retrospective vCJD prevalence study. The Journal of Pathology. 223: 511-8. PMID 21294124 DOI: 10.1002/Path.2821 |
0.325 |
|
| 2011 |
Russo M, Laurá M, Polke JM, Davis MB, Blake J, Brandner S, Hughes RA, Houlden H, Bennett DL, Lunn MP, Reilly MM. Variable phenotypes are associated with PMP22 missense mutations. Neuromuscular Disorders : Nmd. 21: 106-14. PMID 21194947 DOI: 10.1016/J.Nmd.2010.11.011 |
0.323 |
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| 2011 |
Brandner S. Diversity of prion diseases: (no) strains attached? Acta Neuropathologica. 121: 1-4. PMID 21080180 DOI: 10.1007/S00401-010-0775-X |
0.381 |
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| 2011 |
Reiniger L, Lukic A, Linehan J, Rudge P, Collinge J, Mead S, Brandner S. Tau, prions and Aβ: the triad of neurodegeneration. Acta Neuropathologica. 121: 5-20. PMID 20473510 DOI: 10.1007/S00401-010-0691-0 |
0.326 |
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| 2010 |
de Marco MF, Linehan J, Gill ON, Clewley JP, Brandner S. Large-scale immunohistochemical examination for lymphoreticular prion protein in tonsil specimens collected in Britain. The Journal of Pathology. 222: 380-7. PMID 20922767 DOI: 10.1002/Path.2767 |
0.301 |
|
| 2010 |
Lukic A, Beck J, Joiner S, Fearnley J, Sturman S, Brandner S, Wadsworth JD, Collinge J, Mead S. Heterozygosity at polymorphic codon 219 in variant creutzfeldt-jakob disease. Archives of Neurology. 67: 1021-3. PMID 20697057 DOI: 10.1001/Archneurol.2010.184 |
0.355 |
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| 2010 |
Paisán-Ruiz C, Guevara R, Federoff M, Hanagasi H, Sina F, Elahi E, Schneider SA, Schwingenschuh P, Bajaj N, Emre M, Singleton AB, Hardy J, Bhatia KP, Brandner S, Lees AJ, et al. Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations. Movement Disorders : Official Journal of the Movement Disorder Society. 25: 1791-800. PMID 20669327 DOI: 10.1002/Mds.23221 |
0.324 |
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| 2010 |
Edgeworth JA, Gros N, Alden J, Joiner S, Wadsworth JD, Linehan J, Brandner S, Jackson GS, Weissmann C, Collinge J. Spontaneous generation of mammalian prions. Proceedings of the National Academy of Sciences of the United States of America. 107: 14402-6. PMID 20660771 DOI: 10.1073/Pnas.1004036107 |
0.302 |
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| 2010 |
Schott JM, Reiniger L, Thom M, Holton JL, Grieve J, Brandner S, Warren JD, Revesz T. Brain biopsy in dementia: clinical indications and diagnostic approach. Acta Neuropathologica. 120: 327-41. PMID 20640903 DOI: 10.1007/S00401-010-0721-Y |
0.306 |
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| 2010 |
Sandberg MK, Al-Doujaily H, Sigurdson CJ, Glatzel M, O'Malley C, Powell C, Asante EA, Linehan JM, Brandner S, Wadsworth JD, Collinge J. Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein. The Journal of General Virology. 91: 2651-7. PMID 20610667 DOI: 10.1099/Vir.0.024380-0 |
0.351 |
|
| 2010 |
Urwin H, Authier A, Nielsen JE, Metcalf D, Powell C, Froud K, Malcolm DS, Holm I, Johannsen P, Brown J, Fisher EM, van der Zee J, Bruyland M, Van Broeckhoven C, ... ... Brandner S, et al. Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations. Human Molecular Genetics. 19: 2228-38. PMID 20223751 DOI: 10.1093/Hmg/Ddq100 |
0.333 |
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| 2010 |
Jacques TS, Swales A, Brzozowski MJ, Henriquez NV, Linehan JM, Mirzadeh Z, O' Malley C, Naumann H, Alvarez-Buylla A, Brandner S. Combinations of genetic mutations in the adult neural stem cell compartment determine brain tumour phenotypes. The Embo Journal. 29: 222-35. PMID 19927122 DOI: 10.1038/Emboj.2009.327 |
0.32 |
|
| 2010 |
Murphy SM, Polke JM, Manji H, Brandner S, Houlden H, Reilly MM. P59 A novel mutation in the nerve-specific 5 UTR of the Cx32 gene causing CMTX1 Neuromuscular Disorders. 20. DOI: 10.1016/S0960-8966(10)70074-2 |
0.305 |
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| 2009 |
Achilli F, Bros-Facer V, Williams HP, Banks GT, AlQatari M, Chia R, Tucci V, Groves M, Nickols CD, Seburn KL, Kendall R, Cader MZ, Talbot K, van Minnen J, Burgess RW, ... Brandner S, et al. An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy. Disease Models & Mechanisms. 2: 359-73. PMID 19470612 DOI: 10.1242/Dmm.002527 |
0.333 |
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| 2009 |
Asante EA, Gowland I, Grimshaw A, Linehan JM, Smidak M, Houghton R, Osiguwa O, Tomlinson A, Joiner S, Brandner S, Wadsworth JD, Collinge J. Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins. The Journal of General Virology. 90: 546-58. PMID 19218199 DOI: 10.1099/Vir.0.007930-0 |
0.389 |
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| 2008 |
Brandner S, Whitfield J, Boone K, Puwa A, O'Malley C, Linehan JM, Joiner S, Scaravilli F, Calder I, P Alpers M, Wadsworth JD, Collinge J. Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 363: 3755-63. PMID 18849292 DOI: 10.1098/Rstb.2008.0091 |
0.379 |
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| 2008 |
Wadsworth JD, Joiner S, Linehan JM, Asante EA, Brandner S, Collinge J. Review. The origin of the prion agent of kuru: molecular and biological strain typing. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 363: 3747-53. PMID 18849291 DOI: 10.1098/Rstb.2008.0069 |
0.361 |
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| 2008 |
Collinge J, Whitfield J, McKintosh E, Frosh A, Mead S, Hill AF, Brandner S, Thomas D, Alpers MP. A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 363: 3725-39. PMID 18849289 DOI: 10.1098/Rstb.2008.0068 |
0.307 |
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| 2008 |
Webb TE, Poulter M, Beck J, Uphill J, Adamson G, Campbell T, Linehan J, Powell C, Brandner S, Pal S, Siddique D, Wadsworth JD, Joiner S, Alner K, Petersen C, et al. Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series. Brain : a Journal of Neurology. 131: 2632-46. PMID 18757886 DOI: 10.1093/Brain/Awn202 |
0.359 |
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| 2008 |
O'Shea M, Maytham EG, Linehan JM, Brandner S, Collinge J, Lloyd SE. Investigation of mcp1 as a quantitative trait gene for prion disease incubation time in mouse. Genetics. 180: 559-66. PMID 18716327 DOI: 10.1534/Genetics.108.090894 |
0.319 |
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| 2008 |
Isaacs AM, Powell C, Webb TE, Linehan JM, Collinge J, Brandner S. Lack of TAR-DNA binding protein-43 (TDP-43) pathology in human prion diseases. Neuropathology and Applied Neurobiology. 34: 446-56. PMID 18657254 DOI: 10.1111/J.1365-2990.2008.00963.X |
0.354 |
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| 2008 |
White MD, Farmer M, Mirabile I, Brandner S, Collinge J, Mallucci GR. Single treatment with RNAi against prion protein rescues early neuronal dysfunction and prolongs survival in mice with prion disease. Proceedings of the National Academy of Sciences of the United States of America. 105: 10238-43. PMID 18632556 DOI: 10.1073/Pnas.0802759105 |
0.362 |
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| 2008 |
Wadsworth JD, Powell C, Beck JA, Joiner S, Linehan JM, Brandner S, Mead S, Collinge J. Molecular diagnosis of human prion disease. Methods in Molecular Biology (Clifton, N.J.). 459: 197-227. PMID 18576157 DOI: 10.1007/978-1-59745-234-2_14 |
0.372 |
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| 2008 |
Wadsworth JD, Joiner S, Linehan JM, Desbruslais M, Fox K, Cooper S, Cronier S, Asante EA, Mead S, Brandner S, Hill AF, Collinge J. Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice. Proceedings of the National Academy of Sciences of the United States of America. 105: 3885-90. PMID 18316717 DOI: 10.1073/Pnas.0800190105 |
0.359 |
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| 2007 |
Mallucci GR, White MD, Farmer M, Dickinson A, Khatun H, Powell AD, Brandner S, Jefferys JG, Collinge J. Targeting cellular prion protein reverses early cognitive deficits and neurophysiological dysfunction in prion-infected mice. Neuron. 53: 325-35. PMID 17270731 DOI: 10.1016/J.Neuron.2007.01.005 |
0.322 |
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| 2007 |
Nayeem N, Kerr F, Naumann H, Linehan J, Lovestone S, Brandner S. Hyperphosphorylation of tau and neurofilaments and activation of CDK5 and ERK1/2 in PTEN-deficient cerebella. Molecular and Cellular Neurosciences. 34: 400-8. PMID 17208451 DOI: 10.1016/J.Mcn.2006.11.014 |
0.328 |
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| 2007 |
Wadsworth JD, Joiner S, Fox K, Linehan JM, Desbruslais M, Brandner S, Asante EA, Collinge J. Prion infectivity in variant Creutzfeldt-Jakob disease rectum. Gut. 56: 90-4. PMID 16763054 DOI: 10.1136/Gut.2006.091637 |
0.342 |
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| 2006 |
Wroe SJ, Pal S, Siddique D, Hyare H, Macfarlane R, Joiner S, Linehan JM, Brandner S, Wadsworth JD, Hewitt P, Collinge J. Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case report. Lancet. 368: 2061-7. PMID 17161728 DOI: 10.1016/S0140-6736(06)69835-8 |
0.321 |
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| 2006 |
Asante EA, Linehan JM, Gowland I, Joiner S, Fox K, Cooper S, Osiguwa O, Gorry M, Welch J, Houghton R, Desbruslais M, Brandner S, Wadsworth JD, Collinge J. Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous mice. Proceedings of the National Academy of Sciences of the United States of America. 103: 10759-64. PMID 16809423 DOI: 10.1073/Pnas.0604292103 |
0.381 |
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| 2006 |
Wadsworth JD, Joiner S, Linehan JM, Cooper S, Powell C, Mallinson G, Buckell J, Gowland I, Asante EA, Budka H, Brandner S, Collinge J. Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein. Brain : a Journal of Neurology. 129: 1557-69. PMID 16597650 DOI: 10.1093/Brain/Awl076 |
0.365 |
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| 2005 |
Kristiansen M, Messenger MJ, Klöhn PC, Brandner S, Wadsworth JD, Collinge J, Tabrizi SJ. Disease-related prion protein forms aggresomes in neuronal cells leading to caspase activation and apoptosis. The Journal of Biological Chemistry. 280: 38851-61. PMID 16157591 DOI: 10.1074/Jbc.M506600200 |
0.337 |
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| 2005 |
Hafezparast M, Brandner S, Linehan J, Martin JE, Collinge J, Fisher EM. Prion disease incubation time is not affected in mice heterozygous for a dynein mutation. Biochemical and Biophysical Research Communications. 326: 18-22. PMID 15567146 DOI: 10.1016/J.Bbrc.2004.10.206 |
0.367 |
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| 2004 |
Wadsworth JD, Asante EA, Desbruslais M, Linehan JM, Joiner S, Gowland I, Welch J, Stone L, Lloyd SE, Hill AF, Brandner S, Collinge J. Human prion protein with valine 129 prevents expression of variant CJD phenotype. Science (New York, N.Y.). 306: 1793-6. PMID 15539564 DOI: 10.1126/Science.1103932 |
0.353 |
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| 2004 |
Martins LM, Morrison A, Klupsch K, Fedele V, Moisoi N, Teismann P, Abuin A, Grau E, Geppert M, Livi GP, Creasy CL, Martin A, Hargreaves I, Heales SJ, Okada H, ... Brandner S, et al. Neuroprotective role of the Reaper-related serine protease HtrA2/Omi revealed by targeted deletion in mice. Molecular and Cellular Biology. 24: 9848-62. PMID 15509788 DOI: 10.1128/Mcb.24.22.9848-9862.2004 |
0.322 |
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| 2004 |
Frosh A, Smith LC, Jackson CJ, Linehan JM, Brandner S, Wadsworth JD, Collinge J. Analysis of 2000 consecutive UK tonsillectomy specimens for disease-related prion protein. Lancet. 364: 1260-2. PMID 15464187 DOI: 10.1016/S0140-6736(04)17143-2 |
0.315 |
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| 2004 |
Horstmann S, Perry A, Reifenberger G, Giangaspero F, Huang H, Hara A, Masuoka J, Rainov NG, Bergmann M, Heppner FL, Brandner S, Chimelli L, Montagna N, Jackson T, Davis DG, et al. Genetic and expression profiles of cerebellar liponeurocytomas. Brain Pathology (Zurich, Switzerland). 14: 281-9. PMID 15446583 DOI: 10.1111/J.1750-3639.2004.Tb00065.X |
0.328 |
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| 2004 |
Lloyd SE, Linehan JM, Desbruslais M, Joiner S, Buckell J, Brandner S, Wadsworth JD, Collinge J. Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred mice. The Journal of General Virology. 85: 2471-8. PMID 15269389 DOI: 10.1099/Vir.0.79889-0 |
0.338 |
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| 2004 |
Lloyd SE, Thompson SR, Beck JA, Linehan JM, Wadsworth JD, Brandner S, Collinge J, Fisher EM. Identification and characterization of a novel mouse prion gene allele. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 15: 383-9. PMID 15170227 DOI: 10.1007/S00335-004-3041-5 |
0.324 |
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| 2004 |
Anderson L, Rossi D, Linehan J, Brandner S, Weissmann C. Transgene-driven expression of the Doppel protein in Purkinje cells causes Purkinje cell degeneration and motor impairment. Proceedings of the National Academy of Sciences of the United States of America. 101: 3644-9. PMID 15007176 DOI: 10.1073/Pnas.0308681101 |
0.35 |
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| 2003 |
Mallucci G, Dickinson A, Linehan J, Klöhn PC, Brandner S, Collinge J. Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis. Science (New York, N.Y.). 302: 871-4. PMID 14593181 DOI: 10.1126/Science.1090187 |
0.334 |
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| 2003 |
White AR, Enever P, Tayebi M, Mushens R, Linehan J, Brandner S, Anstee D, Collinge J, Hawke S. Monoclonal antibodies inhibit prion replication and delay the development of prion disease. Nature. 422: 80-3. PMID 12621436 DOI: 10.1038/Nature01457 |
0.334 |
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| 2001 |
Masuoka J, Brandner S, Paulus W, Soffer D, Vital A, Chimelli L, Jouvet A, Yonekawa Y, Kleihues P, Ohgaki H. Germline SDHD mutation in paraganglioma of the spinal cord. Oncogene. 20: 5084-6. PMID 11526495 DOI: 10.1038/Sj.Onc.1204579 |
0.305 |
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| 2001 |
Aguzzi A, Brandner S, Fischer MB, Furukawa H, Glatzel M, Hawkins C, Heppner FL, Montrasio F, Navarro B, Parizek P, Pekarik V, Prinz M, Raeber AJ, Röckl C, Klein MA. Spongiform encephalopathies: insights from transgenic models. Advances in Virus Research. 56: 313-52. PMID 11450305 DOI: 10.1016/S0065-3527(01)56032-7 |
0.357 |
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| 2001 |
Behrens A, Brandner S, Genoud N, Aguzzi A. Normal neurogenesis and scrapie pathogenesis in neural grafts lacking the prion protein homologue Doppel. Embo Reports. 2: 347-52. PMID 11306558 DOI: 10.1093/Embo-Reports/Kve088 |
0.368 |
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| 2001 |
Reis RM, Herva R, Brandner S, Koivukangas J, Mironov N, Bär W, Kleihues P, Ohgaki H. Second primary glioblastoma. Journal of Neuropathology and Experimental Neurology. 60: 208-15. PMID 11273008 DOI: 10.1093/Jnen/60.2.208 |
0.323 |
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| 2000 |
Glatzel M, Klein MA, Brandner S, Aguzzi A. Prions: from neurografts to neuroinvasion. Archives of Virology. Supplementum. 3-12. PMID 11214933 DOI: 10.1007/978-3-7091-6308-5_1 |
0.339 |
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| 2000 |
Aguzzi A, Klein MA, Montrasio F, Pekarik V, Brandner S, Furukawa H, Käser P, Röckl C, Glatzel M. Prions: pathogenesis and reverse genetics. Annals of the New York Academy of Sciences. 920: 140-57. PMID 11193143 DOI: 10.1111/J.1749-6632.2000.Tb06916.X |
0.367 |
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| 2000 |
Brandner S, Klein MA, Frigg R, Pekarik V, Parizek P, Raeber A, Glatzel M, Schwarz P, Rülicke T, Weissmann C, Aguzzi A. Neuroinvasion of prions: insights from mouse models. Experimental Physiology. 85: 705-12. PMID 11187965 DOI: 10.1111/J.1469-445X.2000.02091.X |
0.364 |
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| 2000 |
Brandner S, Klein MA, Aguzzi A. [Mechanisms of neuroinvasion by prions: molecular principles and present state of research]. Schweizerische Medizinische Wochenschrift. 130: 435-42. PMID 10780058 DOI: 10.5167/Uzh-1919 |
0.354 |
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| 2000 |
Aguzzi A, Montrasio F, Brandner S, Frigg R, Röckl C, Fischer M, Pekarik V, Furukawa H. Molecular pathology of prion diseases Neurobiology of Aging. 21: 1. DOI: 10.1016/S0197-4580(00)82679-2 |
0.313 |
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| 1999 |
Aguzzi A, Brandner S. The genetics of prions--a contradiction in terms? Lancet. 354: SI22-5. PMID 10437852 DOI: 10.1016/S0140-6736(99)90245-3 |
0.352 |
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| 1999 |
Raeber AJ, Sailer A, Hegyi I, Klein MA, Rülicke T, Fischer M, Brandner S, Aguzzi A, Weissmann C. Ectopic expression of prion protein (PrP) in T lymphocytes or hepatocytes of PrP knockout mice is insufficient to sustain prion replication. Proceedings of the National Academy of Sciences of the United States of America. 96: 3987-92. PMID 10097150 DOI: 10.1073/Pnas.96.7.3987 |
0.337 |
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| 1998 |
Aguzzi A, Klein MA, Musahl C, Raeber AJ, Blättler T, Hegyi I, Frigg R, Brandner S. Use of brain grafts to study the pathogenesis of prion diseases. Essays in Biochemistry. 33: 133-47. PMID 10488447 DOI: 10.1042/Bse0330133 |
0.312 |
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| 1998 |
Raeber AJ, Brandner S, Klein MA, Benninger Y, Musahl C, Frigg R, Roeckl C, Fischer MB, Weissmann C, Aguzzi A. Transgenic and knockout mice in research on prion diseases. Brain Pathology (Zurich, Switzerland). 8: 715-33. PMID 9804380 DOI: 10.1111/J.1750-3639.1998.Tb00197.X |
0.348 |
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| 1998 |
Weissmann C, Fischer M, Raeber A, Büeler H, Sailer A, Shmerling D, Rülicke T, Brandner S, Aguzzi A. The use of transgenic mice in the investigation of transmissible spongiform encephalopathies. Revue Scientifique Et Technique (International Office of Epizootics). 17: 278-90. PMID 9638817 DOI: 10.1007/978-1-4899-1896-3_7 |
0.334 |
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| 1998 |
Kleinle S, Schneider V, Moosmann P, Brandner S, Krähenbühl S, Liechti-Gallati S. A novel mitochondrial tRNA(Phe) mutation inhibiting anticodon stem formation associated with a muscle disease. Biochemical and Biophysical Research Communications. 247: 112-5. PMID 9636664 DOI: 10.1006/Bbrc.1998.8729 |
0.301 |
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| 1998 |
Shmerling D, Hegyi I, Fischer M, Blättler T, Brandner S, Götz J, Rülicke T, Flechsig E, Cozzio A, von Mering C, Hangartner C, Aguzzi A, Weissmann C. Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions. Cell. 93: 203-14. PMID 9568713 DOI: 10.1016/S0092-8674(00)81572-X |
0.351 |
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| 1998 |
Brandner S, Isenmann S, Kühne G, Aguzzi A. Identification of the end stage of scrapie using infected neural grafts. Brain Pathology (Zurich, Switzerland). 8: 19-27. PMID 9458163 DOI: 10.1111/J.1750-3639.1998.Tb00130.X |
0.327 |
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| 1997 |
Raeber AJ, Race RE, Brandner S, Priola SA, Sailer A, Bessen RA, Mucke L, Manson J, Aguzzi A, Oldstone MB, Weissmann C, Chesebro B. Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie. The Embo Journal. 16: 6057-65. PMID 9321385 DOI: 10.1093/Emboj/16.20.6057 |
0.358 |
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| 1997 |
Blättler T, Brandner S, Raeber AJ, Klein MA, Voigtländer T, Weissmann C, Aguzzi A. PrP-expressing tissue required for transfer of scrapie infectivity from spleen to brain. Nature. 389: 69-73. PMID 9288968 DOI: 10.1038/37981 |
0.32 |
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| 1997 |
Aguzzi A, Blättler T, Klein MA, Räber AJ, Hegyi I, Frigg R, Brandner S, Weissmann C. Tracking prions: the neurografting approach. Cellular and Molecular Life Sciences : Cmls. 53: 485-95. PMID 9230924 DOI: 10.1007/S000180050060 |
0.356 |
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| 1996 |
Weissmann C, Fischer M, Raeber A, Büeler H, Sailer A, Shmerling D, Rülicke T, Brandner S, Aguzzi A. The role of PrP in pathogenesis of experimental scrapie. Cold Spring Harbor Symposia On Quantitative Biology. 61: 511-22. PMID 9246477 DOI: 10.1101/Sqb.1996.061.01.051 |
0.309 |
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| 1996 |
Brandner S, Raeber A, Sailer A, Blättler T, Fischer M, Weissmann C, Aguzzi A. Normal host prion protein (PrPC) is required for scrapie spread within the central nervous system. Proceedings of the National Academy of Sciences of the United States of America. 93: 13148-51. PMID 8917559 DOI: 10.1073/Pnas.93.23.13148 |
0.343 |
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| 1996 |
Aguzzi A, Brandner S, Marino S, Steinbach JP. Transgenic and knockout mice in the study of neurodegenerative diseases. Journal of Molecular Medicine (Berlin, Germany). 74: 111-26. PMID 8846161 DOI: 10.1007/Bf01575443 |
0.344 |
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| 1996 |
Fischer M, Rülicke T, Raeber A, Sailer A, Moser M, Oesch B, Brandner S, Aguzzi A, Weissmann C. Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie. The Embo Journal. 15: 1255-64. PMID 8635458 DOI: 10.1002/J.1460-2075.1996.Tb00467.X |
0.332 |
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| 1996 |
Tschopp RR, Brandner S, Marino S, Bothe K, Horak I, Rethwilm A, Aguzzi A. Analysis of the determinants of neurotropism and neurotoxicity of HFV in transgenic mice. Virology. 216: 338-46. PMID 8607263 DOI: 10.1006/Viro.1996.0069 |
0.308 |
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| 1996 |
Fritschy JM, Brandner S, Aguzzi A, Koedood M, Luscher B, Mitchell PJ. Brain cell type specificity and gliosis-induced activation of the human cytomegalovirus immediate-early promoter in transgenic mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 16: 2275-82. PMID 8601807 DOI: 10.1523/Jneurosci.16-07-02275.1996 |
0.325 |
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| 1996 |
Lindberg RL, Porcher C, Grandchamp B, Ledermann B, Bürki K, Brandner S, Aguzzi A, Meyer UA. Porphobilinogen deaminase deficiency in mice causes a neuropathy resembling that of human hepatic porphyria. Nature Genetics. 12: 195-9. PMID 8563760 DOI: 10.1038/Ng0296-195 |
0.305 |
|
| 1996 |
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0.33 |
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| 1994 |
Aguzzi A, Brandner S, Sure U, Rüedi D, Isenmann S. Transgenic and knock-out mice: models of neurological disease. Brain Pathology (Zurich, Switzerland). 4: 3-20. PMID 8025701 DOI: 10.1111/J.1750-3639.1994.Tb00806.X |
0.397 |
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| Show low-probability matches. |
