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 *

392 related articles for article (PubMed ID: 22411239)

  • 21. A New Transgenic Mouse Model of Gerstmann-Straussler-Scheinker Syndrome Caused by the A117V Mutation of PRNP.
    Yang W; Cook J; Rassbach B; Lemus A; DeArmond SJ; Mastrianni JA
    J Neurosci; 2009 Aug; 29(32):10072-80. PubMed ID: 19675240
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129.
    Young K; Clark HB; Piccardo P; Dlouhy SR; Ghetti B
    Brain Res Mol Brain Res; 1997 Feb; 44(1):147-50. PubMed ID: 9030710
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Different Complicated Brain Pathologies in Monozygotic Twins With Gerstmann-Sträussler-Scheinker Disease.
    Honda H; Sasaki K; Takashima H; Mori D; Koyama S; Suzuki SO; Iwaki T
    J Neuropathol Exp Neurol; 2017 Oct; 76(10):854-863. PubMed ID: 28922846
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Divergent clinical and neuropathological phenotype in a Gerstmann-Sträussler-Scheinker P102L family.
    Popova SN; Tarvainen I; Capellari S; Parchi P; Hannikainen P; Pirinen E; Haapasalo H; Alafuzoff I
    Acta Neurol Scand; 2012 Nov; 126(5):315-23. PubMed ID: 22211828
    [TBL] [Abstract][Full Text] [Related]  

  • 25. NGS study in a sicilian case series with a genetic diagnosis for Gerstmann-Sträussler-Scheinker syndrome (PRNP, p.P102L).
    Salemi M; Mandarà LGM; Salluzzo MG; Schillaci FA; Castiglione R; Cordella A; Iorio R; Perrotta CS; Ferri R; Romano C
    Mol Biol Rep; 2023 Nov; 50(11):9715-9720. PubMed ID: 37812352
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient.
    Jansen C; Parchi P; Capellari S; Strammiello R; Dopper EG; van Swieten JC; Kamphorst W; Rozemuller AJ
    J Neuropathol Exp Neurol; 2011 Aug; 70(8):698-702. PubMed ID: 21760536
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Anesthetic management of a patient with Gerstmann-Sträussler-Scheinker syndrome (mutation of prion protein).
    Nakamura M; Ogata M; Matsuo Y; Sata T
    Anesth Analg; 2006 Apr; 102(4):1285-6. PubMed ID: 16551938
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A new point mutation of the PRNP gene in Gerstmann-Sträussler-Scheinker case in Poland.
    Bratosiewicz J; Barcikowska M; Cervenakowa L; Brown P; Gajdusek DC; Liberski PP
    Folia Neuropathol; 2000; 38(4):164-6. PubMed ID: 11693719
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A new PRNP mutation (G131V) associated with Gerstmann-Sträussler-Scheinker disease.
    Panegyres PK; Toufexis K; Kakulas BA; Cernevakova L; Brown P; Ghetti B; Piccardo P; Dlouhy SR
    Arch Neurol; 2001 Nov; 58(11):1899-902. PubMed ID: 11709001
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [A trend of molecular genetics on prion diseases and prion protein].
    Muramatsu Y; Shinagawa M
    Nihon Rinsho; 1993 Sep; 51(9):2494-502. PubMed ID: 8411733
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature.
    Jansen C; Voet W; Head MW; Parchi P; Yull H; Verrips A; Wesseling P; Meulstee J; Baas F; van Gool WA; Ironside JW; Rozemuller AJ
    Acta Neuropathol; 2011 Jan; 121(1):59-68. PubMed ID: 20198483
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prion protein mutation at codon 102 in an Italian family with Gerstmann-Sträussler-Scheinker syndrome.
    Kretzschmar HA; Kufer P; Riethmüller G; DeArmond S; Prusiner SB; Schiffer D
    Neurology; 1992 Apr; 42(4):809-10. PubMed ID: 1348851
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein.
    Asante EA; Linehan JM; Smidak M; Tomlinson A; Grimshaw A; Jeelani A; Jakubcova T; Hamdan S; Powell C; Brandner S; Wadsworth JD; Collinge J
    PLoS Pathog; 2013; 9(9):e1003643. PubMed ID: 24086135
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A Chinese patient of P102L Gerstmann-Sträussler-Scheinker disease contains three other disease-associated mutations in SYNE1.
    Wang J; Xiao K; Zhou W; Gao C; Chen C; Shi Q; Dong XP
    Prion; 2018 Mar; 12(2):150-155. PubMed ID: 29509064
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Transmissibility of Gerstmann-Sträussler-Scheinker syndrome in rodent models: New insights into the molecular underpinnings of prion infectivity.
    Nonno R; Angelo Di Bari M; Agrimi U; Pirisinu L
    Prion; 2016 Nov; 10(6):421-433. PubMed ID: 27892798
    [TBL] [Abstract][Full Text] [Related]  

  • 36. iPS Cell Cultures from a Gerstmann-Sträussler-Scheinker Patient with the Y218N PRNP Mutation Recapitulate tau Pathology.
    Matamoros-Angles A; Gayosso LM; Richaud-Patin Y; di Domenico A; Vergara C; Hervera A; Sousa A; Fernández-Borges N; Consiglio A; Gavín R; López de Maturana R; Ferrer I; López de Munain A; Raya Á; Castilla J; Sánchez-Pernaute R; Del Río JA
    Mol Neurobiol; 2018 Apr; 55(4):3033-3048. PubMed ID: 28466265
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease.
    Parchi P; Chen SG; Brown P; Zou W; Capellari S; Budka H; Hainfellner J; Reyes PF; Golden GT; Hauw JJ; Gajdusek DC; Gambetti P
    Proc Natl Acad Sci U S A; 1998 Jul; 95(14):8322-7. PubMed ID: 9653185
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family.
    De Michele G; Pocchiari M; Petraroli R; Manfredi M; Caneve G; Coppola G; Casali C; Saccà F; Piccardo P; Salvatore E; Berardelli A; Orio M; Barbieri F; Ghetti B; Filla A
    Can J Neurol Sci; 2003 Aug; 30(3):233-6. PubMed ID: 12945948
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cryo-EM structures of prion protein filaments from Gerstmann-Sträussler-Scheinker disease.
    Hallinan GI; Ozcan KA; Hoq MR; Cracco L; Vago FS; Bharath SR; Li D; Jacobsen M; Doud EH; Mosley AL; Fernandez A; Garringer HJ; Jiang W; Ghetti B; Vidal R
    Acta Neuropathol; 2022 Sep; 144(3):509-520. PubMed ID: 35819518
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A family with hereditary cerebellar ataxia finally confirmed as Gerstmann-Straussler-Scheinker syndrome with P102L mutation in PRNP gene.
    Long L; Cai X; Shu Y; Lu Z
    Neurosciences (Riyadh); 2017 Apr; 22(2):138-142. PubMed ID: 28416787
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.