These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

280 related articles for article (PubMed ID: 35978418)

  • 21. Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases.
    Kobayashi A; Parchi P; Yamada M; Mohri S; Kitamoto T
    Neuropathology; 2016 Jun; 36(3):305-10. PubMed ID: 26669818
    [TBL] [Abstract][Full Text] [Related]  

  • 22. V180I genetic Creutzfeldt-Jakob disease: Severe degeneration of the inferior olivary nucleus in an autopsied patient with identification of the M2T prion strain.
    Watanabe M; Nakamura K; Saito R; Takeuchi A; Takahashi T; Kitamoto T; Onodera O; Kakita A
    Neuropathology; 2023 Dec; 43(6):479-485. PubMed ID: 37165430
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cross-sequence transmission of sporadic Creutzfeldt-Jakob disease creates a new prion strain.
    Kobayashi A; Asano M; Mohri S; Kitamoto T
    J Biol Chem; 2007 Oct; 282(41):30022-8. PubMed ID: 17709374
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prion propagation estimated from brain diffusion MRI is subtype dependent in sporadic Creutzfeldt-Jakob disease.
    Pascuzzo R; Oxtoby NP; Young AL; Blevins J; Castelli G; Garbarino S; Cohen ML; Schonberger LB; Gambetti P; Appleby BS; Alexander DC; Bizzi A
    Acta Neuropathol; 2020 Aug; 140(2):169-181. PubMed ID: 32535770
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Large-scale validation of skin prion seeding activity as a biomarker for diagnosis of prion diseases.
    Zhang W; Orrú CD; Foutz A; Ding M; Yuan J; Shah SZA; Zhang J; Kotobelli K; Gerasimenko M; Gilliland T; Chen W; Tang M; Cohen M; Safar J; Xu B; Hong DJ; Cui L; Hughson AG; Schonberger LB; Tatsuoka C; Chen SG; Greenlee JJ; Wang Z; Appleby BS; Caughey B; Zou WQ
    Acta Neuropathol; 2024 Jan; 147(1):17. PubMed ID: 38231266
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Role of prion protein glycosylation in replication of human prions by protein misfolding cyclic amplification.
    Camacho MV; Telling G; Kong Q; Gambetti P; Notari S
    Lab Invest; 2019 Nov; 99(11):1741-1748. PubMed ID: 31249376
    [TBL] [Abstract][Full Text] [Related]  

  • 27. MRI characteristics of sporadic CJD with valine homozygosity at codon 129 of the prion protein gene and PrPSc type 2 in Japan.
    Fukushima R; Shiga Y; Nakamura M; Fujimori J; Kitamoto T; Yoshida Y
    J Neurol Neurosurg Psychiatry; 2004 Mar; 75(3):485-7. PubMed ID: 14966171
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Development of an Automated Capillary Immunoassay to Detect Prion Glycotypes in Creutzfeldt-Jakob Disease.
    Myskiw J; Lamoureux L; Peterson A; Knox D; Jansen GH; Coulthart MB; Booth SA
    Lab Invest; 2023 Mar; 103(3):100029. PubMed ID: 36925197
    [TBL] [Abstract][Full Text] [Related]  

  • 29. MRI lesion profiles in sporadic Creutzfeldt-Jakob disease.
    Meissner B; Kallenberg K; Sanchez-Juan P; Collie D; Summers DM; Almonti S; Collins SJ; Smith P; Cras P; Jansen GH; Brandel JP; Coulthart MB; Roberts H; Van Everbroeck B; Galanaud D; Mellina V; Will RG; Zerr I
    Neurology; 2009 Jun; 72(23):1994-2001. PubMed ID: 19506221
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.
    Parchi P; Cescatti M; Notari S; Schulz-Schaeffer WJ; Capellari S; Giese A; Zou WQ; Kretzschmar H; Ghetti B; Brown P
    Brain; 2010 Oct; 133(10):3030-42. PubMed ID: 20823086
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A traceback phenomenon can reveal the origin of prion infection.
    Kobayashi A; Asano M; Mohri S; Kitamoto T
    Neuropathology; 2009 Oct; 29(5):619-24. PubMed ID: 19659941
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Histotype-Dependent Oligodendroglial PrP Pathology in Sporadic CJD: A Frequent Feature of the M2C "Strain".
    Gelpi E; Klotz S; Vidal-Robau N; Ricken G; Regelsberger G; Ströbel T; Kalev O; Leoni M; Budka H; Kovacs GG
    Viruses; 2021 Sep; 13(9):. PubMed ID: 34578377
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature.
    Rossi M; Saverioni D; Di Bari M; Baiardi S; Lemstra AW; Pirisinu L; Capellari S; Rozemuller A; Nonno R; Parchi P
    Acta Neuropathol Commun; 2017 Nov; 5(1):87. PubMed ID: 29169405
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.
    Faucheux BA; Morain E; Diouron V; Brandel JP; Salomon D; Sazdovitch V; Privat N; Laplanche JL; Hauw JJ; Haïk S
    Neuropathol Appl Neurobiol; 2011 Aug; 37(5):500-12. PubMed ID: 21450052
    [TBL] [Abstract][Full Text] [Related]  

  • 35. MM2-thalamic Creutzfeldt-Jakob disease: neuropathological, biochemical and transmission studies identify a distinctive prion strain.
    Moda F; Suardi S; Di Fede G; Indaco A; Limido L; Vimercati C; Ruggerone M; Campagnani I; Langeveld J; Terruzzi A; Brambilla A; Zerbi P; Fociani P; Bishop MT; Will RG; Manson JC; Giaccone G; Tagliavini F
    Brain Pathol; 2012 Sep; 22(5):662-9. PubMed ID: 22288561
    [TBL] [Abstract][Full Text] [Related]  

  • 36. An autopsied case of MM1 + MM2-cortical with thalamic-type sporadic Creutzfeldt-Jakob disease presenting with hyperintensities on diffusion-weighted MRI before clinical onset.
    Iwasaki Y; Mori K; Ito M; Mimuro M; Kitamoto T; Yoshida M
    Neuropathology; 2017 Feb; 37(1):78-85. PubMed ID: 27436355
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene.
    Di Fede G; Catania M; Atzori C; Moda F; Pasquali C; Indaco A; Grisoli M; Zuffi M; Guaita MC; Testi R; Taraglio S; Sessa M; Gusmaroli G; Spinelli M; Salzano G; Legname G; Tarletti R; Godi L; Pocchiari M; Tagliavini F; Imperiale D; Giaccone G
    Acta Neuropathol Commun; 2019 Jan; 7(1):1. PubMed ID: 30606247
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British woman.
    Mead S; Joiner S; Desbruslais M; Beck JA; O'Donoghue M; Lantos P; Wadsworth JD; Collinge J
    Arch Neurol; 2007 Dec; 64(12):1780-4. PubMed ID: 18071044
    [TBL] [Abstract][Full Text] [Related]  

  • 39. An autopsied case of MV2K + C-type sporadic Creutzfeldt-Jakob disease presenting with widespread cerebral cortical involvement and Kuru plaques.
    Iwasaki Y; Saito Y; Aiba I; Kobayashi A; Mimuro M; Kitamoto T; Yoshida M
    Neuropathology; 2017 Jun; 37(3):241-248. PubMed ID: 28568896
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease.
    Worrall BB; Herman ST; Capellari S; Lynch T; Chin S; Gambetti P; Parchi P
    J Neurol Neurosurg Psychiatry; 1999 Nov; 67(5):671-4. PubMed ID: 10519879
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.