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 *

134 related articles for article (PubMed ID: 28899992)

  • 41. Convulsive responses to seizure-inducible drugs are exacerbated in progranulin-deficient mice.
    Kuroda M; Matsuwaki T; Tanaka Y; Yamanouchi K; Nishihara M
    Neuroreport; 2020 Apr; 31(6):478-483. PubMed ID: 32168097
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Endocytosis of GluN2B-containing NMDA receptors mediates NMDA-induced excitotoxicity.
    Wu Y; Chen C; Yang Q; Jiao M; Qiu S
    Mol Pain; 2017 Jan; 13():1744806917701921. PubMed ID: 28326942
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Tau is required for the function of extrasynaptic NMDA receptors.
    Pallas-Bazarra N; Draffin J; Cuadros R; Antonio Esteban J; Avila J
    Sci Rep; 2019 Jun; 9(1):9116. PubMed ID: 31235881
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Conditional loss of progranulin in neurons is not sufficient to cause neuronal ceroid lipofuscinosis-like neuropathology in mice.
    Petkau TL; Blanco J; Leavitt BR
    Neurobiol Dis; 2017 Oct; 106():14-22. PubMed ID: 28647554
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Local Somatodendritic Translation and Hyperphosphorylation of Tau Protein Triggered by AMPA and NMDA Receptor Stimulation.
    Kobayashi S; Tanaka T; Soeda Y; Almeida OFX; Takashima A
    EBioMedicine; 2017 Jun; 20():120-126. PubMed ID: 28566250
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Higher levels of phosphorylated Y1472 on GluN2B subunits in the frontal cortex of aged mice are associated with good spatial reference memory, but not cognitive flexibility.
    Zamzow DR; Elias V; Acosta VA; Escobedo E; Magnusson KR
    Age (Dordr); 2016 Jun; 38(3):50. PubMed ID: 27094400
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Single-neuron NMDA receptor phenotype influences neuronal rewiring and reintegration following traumatic injury.
    Patel TP; Ventre SC; Geddes-Klein D; Singh PK; Meaney DF
    J Neurosci; 2014 Mar; 34(12):4200-13. PubMed ID: 24647941
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Lipidomic and Transcriptomic Basis of Lysosomal Dysfunction in Progranulin Deficiency.
    Evers BM; Rodriguez-Navas C; Tesla RJ; Prange-Kiel J; Wasser CR; Yoo KS; McDonald J; Cenik B; Ravenscroft TA; Plattner F; Rademakers R; Yu G; White CL; Herz J
    Cell Rep; 2017 Sep; 20(11):2565-2574. PubMed ID: 28903038
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Progranulin Deficiency Reduces CDK4/6/pRb Activation and Survival of Human Neuroblastoma SH-SY5Y Cells.
    de la Encarnación A; Alquézar C; Esteras N; Martín-Requero Á
    Mol Neurobiol; 2015 Dec; 52(3):1714-1725. PubMed ID: 25377796
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration.
    Krüger J; Kaivorinne AL; Udd B; Majamaa K; Remes AM
    Eur J Neurol; 2009 Jan; 16(1):27-30. PubMed ID: 19049508
    [TBL] [Abstract][Full Text] [Related]  

  • 51. GluN2B-containing NMDA receptors are upregulated in plasma membranes by the sphingosine-1-phosphate analog FTY720P.
    Attiori Essis S; Laurier-Laurin ME; Pépin É; Cyr M; Massicotte G
    Brain Res; 2015 Oct; 1624():349-358. PubMed ID: 26260438
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Core neuropathological abnormalities in progranulin-deficient mice are penetrant on multiple genetic backgrounds.
    Petkau TL; Hill A; Leavitt BR
    Neuroscience; 2016 Feb; 315():175-95. PubMed ID: 26701296
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Disulfide-containing high mobility group box-1 promotes N-methyl-D-aspartate receptor function and excitotoxicity by activating Toll-like receptor 4-dependent signaling in hippocampal neurons.
    Balosso S; Liu J; Bianchi ME; Vezzani A
    Antioxid Redox Signal; 2014 Oct; 21(12):1726-40. PubMed ID: 24094148
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide.
    Benussi L; Ghidoni R; Pegoiani E; Moretti DV; Zanetti O; Binetti G
    Neurobiol Dis; 2009 Mar; 33(3):379-85. PubMed ID: 19101631
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Opposing role of NMDA receptor GluN2B and GluN2D in somatosensory development and maturation.
    Yamasaki M; Okada R; Takasaki C; Toki S; Fukaya M; Natsume R; Sakimura K; Mishina M; Shirakawa T; Watanabe M
    J Neurosci; 2014 Aug; 34(35):11534-48. PubMed ID: 25164652
    [TBL] [Abstract][Full Text] [Related]  

  • 56. The GluN2B subunit represents a major functional determinant of NMDA receptors in human induced pluripotent stem cell-derived cortical neurons.
    Neagoe I; Liu C; Stumpf A; Lu Y; He D; Francis R; Chen J; Reynen P; Alaoui-Ismaili MH; Fukui H
    Stem Cell Res; 2018 Apr; 28():105-114. PubMed ID: 29454156
    [TBL] [Abstract][Full Text] [Related]  

  • 57. The lysosomal protein cathepsin L is a progranulin protease.
    Lee CW; Stankowski JN; Chew J; Cook CN; Lam YW; Almeida S; Carlomagno Y; Lau KF; Prudencio M; Gao FB; Bogyo M; Dickson DW; Petrucelli L
    Mol Neurodegener; 2017 Jul; 12(1):55. PubMed ID: 28743268
    [TBL] [Abstract][Full Text] [Related]  

  • 58. A novel phosphorylation site of N-methyl-D-aspartate receptor GluN2B at S1284 is regulated by Cdk5 in neuronal ischemia.
    Lu W; Ai H; Peng L; Wang JJ; Zhang B; Liu X; Luo JH
    Exp Neurol; 2015 Sep; 271():251-8. PubMed ID: 26093036
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Mutations in progranulin gene: clinical, pathological, and ribonucleic acid expression findings.
    López de Munain A; Alzualde A; Gorostidi A; Otaegui D; Ruiz-Martínez J; Indakoetxea B; Ferrer I; Pérez-Tur J; Sáenz A; Bergareche A; Barandiarán M; Poza JJ; Zabalza R; Ruiz I; Urtasun M; Fernández-Manchola I; Olasagasti B; Espinal JB; Olaskoaga J; Ruibal M; Moreno F; Carrera N; Martí Massó JF
    Biol Psychiatry; 2008 May; 63(10):946-52. PubMed ID: 17950702
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The molecular genetics and neuropathology of frontotemporal lobar degeneration: recent developments.
    Mackenzie IR; Rademakers R
    Neurogenetics; 2007 Nov; 8(4):237-48. PubMed ID: 17805587
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.